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Choroid plexus

The choroid plexus is a specialized neuroepithelial tissue located within the ventricles of the brain, consisting of a network of fenestrated capillaries enveloped by cuboidal epithelial cells that produce cerebrospinal fluid (CSF) and form the blood-CSF barrier. This structure plays a critical role in maintaining brain homeostasis by secreting CSF, which cushions the central nervous system, facilitates nutrient transport, removes metabolic waste, and provides immune surveillance.^[1] Anatomically, the choroid plexus lines the lateral, third, and fourth ventricles of the brain, though it is absent from certain regions such as the frontal and occipital horns of the lateral ventricles and the cerebral aqueduct. It is composed of a vascular core derived from the pia mater, surrounded by a single layer of ependymal epithelial cells connected by tight junctions, which exhibit microvilli and cilia to enhance CSF secretion and circulation. The epithelial cells actively transport ions, water, and solutes from the bloodstream into the ventricular space, generating approximately 500 mL of CSF per day in adults, with only a small fraction (about 150 mL) present in the ventricular system at any time due to continuous circulation and absorption.^[1] Beyond CSF production, the choroid plexus serves diverse physiological functions essential for brain health. It acts as a selective barrier, preventing the entry of pathogens, toxins, and large molecules into the CSF while allowing the passage of essential nutrients, hormones, and growth factors such as insulin-like growth factor and fibroblast growth factor. The structure also contributes to immune modulation by facilitating leukocyte trafficking and cytokine signaling, particularly during neuroinflammation or aging, where it shifts immune responses toward anti-inflammatory profiles. Additionally, it influences neural stem cell behavior and neurogenesis through secreted signaling molecules in the CSF, supporting brain development and repair processes.^[1]^[2] Embryologically, the choroid plexus develops early in gestation from interactions between neuroectodermal and mesodermal tissues, beginning around the fifth to seventh week, and matures to support fetal CSF dynamics critical for brain growth. Dysfunctions in choroid plexus function are implicated in conditions such as hydrocephalus, often linked to overproduction of CSF or barrier disruptions, highlighting its integral role in neurological homeostasis.^[1]^[3]

Anatomy

Location and gross anatomy

The choroid plexus is a highly vascularized structure present in all four cerebral ventricles of the brain: the paired lateral ventricles (one in each cerebral hemisphere), the third ventricle, and the fourth ventricle.^[1] In the lateral ventricles, it extends along the body (choroidal zone), into the temporal horn (inferior choroidal zone), and reaches the atrium (glomus), forming continuous but segmented projections.^[4] The third ventricle contains a smaller, midline plexus located along the roof, protruding through the tela choroidea.^[1] In the fourth ventricle, the plexus occupies the roof and extends into the lateral recesses, appearing as irregular tufts on either side of the midline.^[1] Macroscopically, the choroid plexus consists of frond-like, villous projections that form a cauliflower-like mass, with a tufted and highly folded appearance due to its vascular core enveloped by epithelial cells.^[5] It varies in size and compactness across ventricles, being the largest and most extensive in the lateral ventricles, smaller and less elaborate in the third ventricle, and more compact in the fourth ventricle.^[5] These structures are suspended within the ventricular lumen, increasing surface area for interaction with cerebrospinal fluid. The vascular supply to the choroid plexus arises from branches of the internal carotid and vertebrobasilar systems.^[1] The lateral ventricular plexuses receive blood primarily from the anterior choroidal artery (a branch of the internal carotid artery) and the lateral posterior choroidal artery (from the posterior cerebral artery), while the third ventricular plexus is supplied by the medial posterior choroidal artery (also from the posterior cerebral artery).^[4] The fourth ventricular plexus is fed by the posterior inferior cerebellar artery (from the vertebrobasilar system).^[1] Nervous innervation to the choroid plexus is sparse and primarily autonomic, with sympathetic fibers originating from the superior cervical ganglion to regulate blood flow, and parasympathetic input that may influence vascular tone.^[4] Related structures include arachnoid granulations, which are outgrowths of the arachnoid mater involved in cerebrospinal fluid reabsorption and functionally complement the choroid plexus in cerebrospinal fluid dynamics.^[1]

Histology and ultrastructure

The choroid plexus exhibits a specialized layered structure consisting of fenestrated endothelium lining the capillaries, a basement membrane, a connective tissue stroma containing capillaries, and an apical layer of cuboidal to columnar epithelial cells.^[6] This organization facilitates the selective passage of plasma ultrafiltrate while establishing a barrier to larger molecules. The epithelial cells form a single polarized monolayer, characterized by numerous microvilli on their apical surface facing the cerebrospinal fluid, which greatly increases the surface area for exchange—approximately 15-fold across species.^[7] These cells also feature cilia that contribute to cerebrospinal fluid circulation and extensive basolateral infoldings that enhance transport capacity.^[6] At the ultrastructural level, tight junctions, specifically zonula occludens composed of occludins, claudins, and junctional adhesion molecules, seal the intercellular spaces between epithelial cells, forming the primary structural basis of the blood–cerebrospinal fluid barrier.^[6] Gap junctions, mediated by connexins, enable intercellular communication, while the abundance of mitochondria reflects the high metabolic activity required for epithelial functions. The predominant cell type is the choroid epithelial cell.^[6] Minor populations include fibroblasts, immune cells such as macrophages and dendritic cells, and pericytes associated with the vasculature.^[6] The stroma comprises loose connective tissue rich in collagen and elastin fibers, interspersed with fenestrated capillaries that permit the diffusion of water, ions, and small molecules from the plasma.^[6] Epithelial cells contain notable glycogen stores for energy support and express carbonic anhydrase, which facilitates ion transport processes.

Development

Embryonic development

The choroid plexus begins to form during early human embryogenesis through invagination of the roof plate of the neural tube into the developing ventricles, shortly after neural tube closure around week 4 of gestation.^[8] This structure arises from neuroectoderm, which gives rise to the epithelial cells, while the underlying stroma derives from mesenchyme of mesodermal origin.^[9] The process starts in the fourth ventricle at approximately 6 weeks gestation (corresponding to a crown-rump length of about 16 mm), followed by the lateral ventricles around 7 weeks (19 mm), and the third ventricle at about 8 weeks (23 mm).^[8] Key developmental processes include the protrusion of mesenchymal tissue and capillaries into the ventricular lumen, leading to vascularization via angiogenic invasion from surrounding mesoderm, and the differentiation of epithelial cells from ependymal precursors into a polarized, cuboidal layer.^[9]^[10] In humans, the lateral ventricular choroid plexus undergoes four histological stages: stage I (week 7) features pseudostratified epithelium without glycogen or villi; stage II (week 9) shows glycogen-laden columnar cells with sparse microvilli; stage III (week 17) has cuboidal cells with microvilli and moderate glycogen; and stage IV (week 29) exhibits mature cuboidal cells lacking glycogen.^[11] Recent studies as of 2025 have identified additional molecular mechanisms in embryonic choroid plexus development. Apocrine secretion by choroid plexus epithelial cells regulates the cerebrospinal fluid (CSF) proteome, influencing neurodevelopment in mice, a process likely conserved in humans. Furthermore, epithelial cells emerge sequentially with distinct subtypes that contract over time, contributing to functional maturation.^[12]^[13] Molecular regulation is orchestrated by signaling pathways and transcription factors that specify choroid plexus fate in the dorsal neural tube. Bone morphogenetic protein (BMP) signaling, particularly BMP4, from the roof plate induces epithelial differentiation and proliferation while suppressing alternative fates.^[10] Transcription factors such as Lmx1a and Lmx1b are essential for roof plate formation and initial specification, with their expression overlapping markers like transthyretin (Ttr); Otx2 plays a temporal role in patterning, where early deletion abolishes all plexuses and later deletion affects hindbrain development.^[9]^[10] Wnt signaling, elevated in regions like the cortical hem, promotes branching in the fourth ventricle via factors such as Wnt1 and MEIS1-WNT5A, while Sonic hedgehog (Shh) gradients regulate vascular outgrowth and progenitor proliferation in the hindbrain plexus through autoregulatory loops.^[10]^[8] The developmental program is conserved across vertebrates, including mice, chicks, and zebrafish, where the sequential formation (hindbrain first, then forebrain) and reliance on BMP, Wnt, and Shh are similar; however, human lateral plexuses are more voluminous and complex compared to rodents, filling a larger proportion of the ventricles early on.^[10]^[9] Disruptions in these processes can lead to agenesis or hypoplasia of the choroid plexus, often associated with neural tube defects such as anencephaly, where failure of anterior neural tube closure results in absence of forebrain structures, including the lateral and third ventricular plexuses.^[14]^[15]

Postnatal development

Following birth, the choroid plexus exhibits rapid growth that parallels the expansion of the brain and ventricular system during infancy and early childhood. In humans, choroid plexus volume increases markedly from birth, reaching approximately 1.5 mL by around 1 year of age, after which it stabilizes and remains relatively constant through adolescence, while intracranial volume continues to grow until about 20 months. This growth supports the maturation of cerebrospinal fluid (CSF) dynamics, with production rates rising dramatically in the early postnatal period—evidence from rodent models indicates a sharp increase during the second postnatal week, achieving adult-like levels before weaning, a pattern extrapolated to humans where rates approach adult values (around 0.3–0.4 mL/min) by 1–2 years of age.^[16]^[10]^[17] In adulthood, the choroid plexus maintains a stable size with minor regional variations across the lateral, third, and fourth ventricles, reflecting its established role in steady-state CSF production of approximately 500–600 mL per day. Calcification commonly begins in the stromal tissue during this period and is observed in approximately 70% of adults, increasing with age and often appearing as incidental findings on imaging without functional impairment.^[18] Hormonal factors contribute to this stability and maturation; thyroid hormones and glucocorticoids promote epithelial differentiation and functional readiness postnatally, while sex differences emerge, with males typically exhibiting larger choroid plexus volumes than females, potentially influencing CSF composition and barrier properties.^[17]^[19]^[20] During aging, the choroid plexus undergoes progressive structural changes, including atrophy, fibrosis, and reductions in epithelial cell height and microvilli density. Studies from 2003 reported a notable decline in CSF production, from about 0.4 mL/min in young adults to approximately 0.2 mL/min in the elderly (particularly octogenarians), representing a reduction of up to 50%, alongside decreased enzymatic activity in epithelial cells. However, a 2025 study in rats found CSF secretion remains largely stable in healthy aging, suggesting the decline in humans may be less pronounced or influenced by health status, warranting further research. The regenerative capacity remains limited, with sparse stem cell populations in the epithelium, though choroid plexus epithelial cells can proliferate modestly in response to injury or growth factors, aiding partial repair without robust renewal. Comparatively, the choroid plexus occupies a larger relative volume in neonates compared to adults, facilitating higher CSF turnover rates essential for early brain development and nutrient delivery.^[21]^[22]^[23]^[10]^[24]

Physiology

Cerebrospinal fluid production

The choroid plexus is the primary site of cerebrospinal fluid (CSF) production in the brain, generating approximately 400–600 mL per day in adults, equivalent to about 0.3–0.4 mL/min, which accounts for 70–80% of total CSF production.^[25]^[3] The resulting CSF has a composition similar to plasma ultrafiltrate but with notably lower concentrations of proteins and potassium, alongside higher levels of sodium and chloride ions.^[3]^[26] CSF secretion occurs through active transport processes across the polarized choroid plexus epithelium, where blood plasma components are selectively modified into CSF. The basolateral membrane of these epithelial cells features Na+/K+-ATPase pumps that actively extrude sodium ions into the interstitial space, establishing an electrochemical gradient that drives subsequent ion movements.^[27] This gradient facilitates sodium entry at the apical membrane via Na+/H+ exchangers, coupled with chloride ion transport through dedicated channels, leading to net fluid secretion into the ventricular space.^[27]^[28] Central to ion transport is the role of carbonic anhydrase enzymes, which catalyze the formation of bicarbonate (HCO3-) from carbon dioxide and water, enabling chloride entry via associated transporters; isoforms II (cytosolic) and IV (membrane-bound) are prominently expressed in the choroid plexus epithelium.^[27]^[29] Key transporters include the Na+-K+-2Cl- cotransporter (NKCC1) on the apical membrane, which contributes substantially to chloride and sodium uptake for secretion, and the Na+/HCO3- cotransporter on the basolateral side, which supports bicarbonate efflux.^[30]^[27] Water movement follows this osmotic gradient primarily through aquaporin-1 (AQP1) channels abundantly localized in the apical membrane.^[27] Regulation of CSF production involves multiple physiological inputs, including autonomic innervation, where vagal (parasympathetic) stimulation enhances secretion rates.^[31] Hormonally, arginine vasopressin inhibits production via V1 receptors on the choroid plexus epithelium, reducing fluid secretion in response to osmotic signals.^[32] The process is also sensitive to plasma osmolarity, with the epithelium adjusting transport activity to maintain CSF homeostasis even against opposing gradients.^[33] Additionally, CSF production exhibits circadian rhythms, with elevated rates during the dark phase (active phase in nocturnal rodents and rest phase in diurnal humans), potentially linked to autonomic and transcriptional oscillations in the choroid plexus.^[34]^[35]

Blood–cerebrospinal fluid barrier

The blood–cerebrospinal fluid (B-CSF) barrier is primarily formed by the epithelial cells of the choroid plexus, which are sealed by tight junctions that prevent paracellular diffusion of substances between the blood and cerebrospinal fluid (CSF). These tight junctions include proteins such as occludin, which contributes to sealing the intercellular spaces, and claudins 1, 2, and 11, which are expressed in the choroid plexus epithelium to regulate paracellular permeability.^[36]^[37] In contrast to the blood–brain barrier (BBB), the endothelium of choroid plexus capillaries is fenestrated, lacking tight junctions and allowing free filtration of plasma components into the interstitial space before selective passage across the epithelial layer.^[38] The B-CSF barrier exhibits selective permeability, excluding large molecules greater than approximately 500 Da and immune cells while permitting the diffusion of small ions, water, and essential nutrients such as glucose.^[39] Active transport mechanisms further control substance exchange: influx transporters include GLUT1 for glucose uptake from blood and OAT3 for organic anions at the apical (CSF-facing) membrane, whereas efflux transporters such as P-glycoprotein (MDR1) and MRP1 export drugs, toxins, and xenobiotics back into the bloodstream to protect the CNS.^[38]^[40]^[41] Compared to the BBB, the B-CSF barrier is more permeable to small hydrophilic molecules and ions like calcium (with a tenfold higher influx rate) due to its fenestrated endothelium and distinct transporter profile, though both barriers share similar efflux pumps; additionally, the barrier is sensitive to pH differences, with CSF maintaining a slightly more alkaline pH (~7.3) than blood (~7.4), influencing ion transport.^[38]^[42] Regulation of the B-CSF barrier involves dynamic responses to physiological and pathological signals; for instance, inflammatory cytokines like TNF-α can disrupt tight junctions by downregulating occludin and activating matrix metalloproteinases, thereby increasing permeability.^[43] Thyroid hormones promote barrier maturation during development by enhancing epithelial tight junction integrity, though specific mechanisms in the choroid plexus remain under investigation.^[44] In clinical diagnostics, disruption of the B-CSF barrier is indicated by leakage of gadolinium-based contrast agents into the CSF on MRI, often observed in conditions like meningitis or neuroinflammation, signaling impaired selectivity.^[45]

Other physiological roles

The choroid plexus plays a critical role in immune surveillance within the central nervous system, secreting cytokines such as interleukin-6 (IL-6) and transforming growth factor-β (TGF-β), as well as complement proteins, to modulate inflammatory responses and maintain immune homeostasis.^[46]^[47] These secretions help detect pathogens and respond to changes in the cytokine milieu, facilitating coordinated immune signaling across the blood-CSF interface.^[48] Resident macrophages, often termed epiplexus cells or Kolmer cells, populate the choroid plexus and perform phagocytosis of cellular debris and pathogens, contributing to debris clearance in the cerebrospinal fluid (CSF).^[49] Additionally, the choroid plexus supports T-cell trafficking into the CSF, acting as a gateway for adaptive immune cells to patrol the brain's ventricular spaces and respond to threats.^[50] In neuroendocrine functions, the choroid plexus synthesizes transthyretin (TTR), a transport protein that binds thyroxine (T4) to facilitate its delivery from blood to brain parenchyma via the CSF, ensuring thyroid hormone availability for neural development and metabolism.^[51] It also serves as a local source of melatonin, expressing enzymes for its biosynthesis and contributing to elevated melatonin levels in the CSF, which supports circadian regulation and antioxidant defense in the brain.^[52] Furthermore, the choroid plexus is responsive to hormones like leptin, expressing receptors that mediate its transport across the blood-CSF barrier, thereby influencing energy balance and hypothalamic signaling.^[53] The choroid plexus contributes to waste clearance by integrating with the glymphatic system, where CSF flow driven by choroid plexus activity promotes the removal of metabolic byproducts from brain interstitial spaces.^[54] It facilitates the efflux of amyloid-β peptides through receptors such as low-density lipoprotein receptor-related protein 1 (LRP1), which binds and internalizes these proteins for clearance from the CSF, helping prevent protein aggregation in neurodegenerative contexts.^[55] During development, the choroid plexus provides essential signaling molecules to the embryonic CSF, including insulin-like growth factor 2 (IGF-2), which regulates neurogenesis, cortical layering, and overall brain size by promoting progenitor proliferation and neuronal differentiation.^[25] Retinoic acid secreted by the choroid plexus also guides neuronal migration from proliferative zones like the ganglionic eminence to cortical targets, supporting circuit formation and regional brain patterning.^[56]^[57] In metabolic homeostasis, the choroid plexus expresses glucose transporters that sense and regulate glucose influx into the CSF, maintaining a favorable gradient for brain energy supply despite high neural consumption.^[58] It transports insulin across the blood-CSF barrier and may produce it locally in epithelial cells, responding to serotonergic signals to modulate systemic glucose regulation.^[59] Additionally, through bicarbonate (HCO₃⁻) secretion and ion transport mechanisms, the choroid plexus buffers CSF pH, stabilizing the brain's chemical environment against fluctuations.^[60] Emerging research highlights the choroid plexus as a site of circadian rhythmicity, with epithelial cells expressing clock genes like Period 2 (Per2) that drive oscillatory gene expression and influence broader brain rhythms, including CSF dynamics and immune activity.^[61] This internal clock synchronizes with feeding cues and glucocorticoids, underscoring the choroid plexus's role in temporally coordinated brain homeostasis.^[62]

Clinical significance

Congenital anomalies and cysts

Choroid plexus cysts (CPCs) are benign, fluid-filled sacs that form within the choroid plexus of the lateral ventricles during fetal development.^[63] They arise from the invagination of neuroepithelium lining the interlobar clefts into the stroma, resulting in the accumulation of cerebrospinal fluid (CSF) and cellular debris.^[64] These cysts are typically transient and occur in approximately 1-2% of fetuses during the second trimester, with a prevalence of about 1 in 50 at 20 weeks' gestation.^[65] They range in size from 2 mm to 20 mm, though most are smaller than 10 mm, and more than 90% resolve spontaneously by 26-28 weeks of gestation or by birth.^[66] ^[64] Isolated CPCs are generally benign and not associated with adverse outcomes, but their presence warrants evaluation for chromosomal abnormalities, particularly when multiple, bilateral, larger than 10 mm, or accompanied by other sonographic soft markers.^[67] Such findings increase the risk for trisomy 18 (Edwards syndrome), with approximately three-fourths of aneuploidies linked to CPCs being this condition, and a smaller proportion involving trisomy 21.^[68] The pathogenesis may relate to incomplete regression of embryonic invaginations of the neuroepithelium, a process that briefly references normal choroid plexus formation during early gestation.^[64] Diagnosis of CPCs primarily occurs via prenatal ultrasound in the second trimester, appearing as single or multiple anechoic cystic areas greater than 2 mm in diameter within the choroid plexuses of one or both lateral ventricles.^[66] If concerns arise, fetal magnetic resonance imaging (MRI) can provide additional detail, while postnatal cysts are often incidental findings on neuroimaging.^[65] Management involves serial ultrasound monitoring to confirm resolution, with genetic counseling and amniocentesis recommended if risk factors for aneuploidy are present; surgical intervention, such as fenestration, is rare and reserved for symptomatic cases causing ventricular obstruction or hydrocephalus.^[69] ^[70] Other congenital anomalies of the choroid plexus include rare presentations of choroid plexus papilloma in neonates, which can manifest as space-occupying lesions shortly after birth.^[71] Additionally, severe holoprosencephaly may involve distorted or fused choroid plexuses due to failed prosencephalic cleavage, leading to abnormal ventricular structures.^[72]

Neoplasms

Choroid plexus neoplasms, also known as choroid plexus tumors (CPTs), are rare intraventricular tumors arising from the choroidal epithelium, classified by the World Health Organization (WHO) into three main types based on histological and molecular features: choroid plexus papilloma (CPP, WHO grade I, benign), atypical choroid plexus papilloma (aCPP, WHO grade II, intermediate), and choroid plexus carcinoma (CPC, WHO grade III, malignant).^[73] CPP accounts for approximately 80% of all CPTs and is characterized by well-differentiated papillary structures resembling normal choroid plexus, while CPC represents about 20% and exhibits aggressive features such as brain invasion and high mitotic activity.^[74] These tumors primarily occur within the cerebral ventricles, with CPP and CPC in children often located in the lateral ventricles and those in adults more frequently in the fourth ventricle.^[75] Epidemiologically, CPTs are uncommon, comprising 1-4% of all childhood brain tumors and up to 2-6% of those in pediatric patients, with an incidence of about 0.03 per 100,000 in adults.^[76] They predominantly affect young children, with over 70% diagnosed before age 2 years, particularly in the first year of life where they represent more than 10% of brain tumors; adult cases are rarer and typically occur in the fourth decade.^[77] Risk factors include germline TP53 mutations, as seen in Li-Fraumeni syndrome, which are associated with up to 40% of pediatric CPC cases.^[78] Pathologically, CPP originates from epithelial cell hyperplasia forming frond-like projections covered by a single layer of cuboidal epithelium without atypia or invasion, maintaining a low proliferative index.^[79] In contrast, CPC demonstrates malignant transformation with increased cellularity, nuclear pleomorphism, frequent mitoses exceeding 5 per 10 high-power fields, necrosis, and brain parenchymal invasion; somatic TP53 mutations occur in 36-60% of CPCs, contributing to genomic instability and poorer outcomes.^[80] ACPP serves as an intermediate entity with moderate atypia, elevated mitotic rates (2-5 per 10 high-power fields), and occasional brain invasion but lacks the full malignant criteria of CPC.^[81] Clinical symptoms of choroid plexus neoplasms often result from hydrocephalus due to cerebrospinal fluid (CSF) overproduction by the tumor or obstruction of CSF pathways, leading to increased intracranial pressure.^[74] Common presentations include headaches, vomiting, nausea, irritability, seizures, and visual disturbances such as blurred or double vision, particularly in infants where bulging fontanelles and lethargy may predominate.^[82] Diagnosis relies on neuroimaging, with magnetic resonance imaging (MRI) revealing a vividly enhancing, lobulated, cauliflower-like intraventricular mass that is iso- to hyperintense on T1 and T2 sequences, often accompanied by hydrocephalus.^[83] Computed tomography (CT) may show calcification or hemorrhage, while CSF cytology can detect malignant cells in CPC, aiding in distinguishing neoplastic from non-neoplastic lesions; histopathological confirmation via biopsy is essential for WHO grading.^[84] Treatment centers on maximal safe surgical resection, which is curative for most CPP and aCPP cases, with gross total resection achieving excellent control due to their well-circumscribed nature.^[85] For CPC, surgery is followed by adjuvant chemotherapy regimens including cisplatin, etoposide, and cyclophosphamide, particularly in children to delay or avoid radiation; radiation therapy is reserved for incomplete resections or recurrent disease but is cautiously used in young patients due to neurocognitive risks. As of 2025, ongoing research explores targeted therapies, including TP53 inhibitors and immunotherapies, to improve outcomes in TP53-mutated CPC cases.^[77]^[86] Prognosis varies markedly by tumor grade: CPP has a near 100% 5-year survival rate with complete resection, while aCPP exceeds 80%, and CPC ranges from 40-60% 5-year survival, influenced by extent of resection, TP53 status, and multimodal therapy.^[87] Early diagnosis and aggressive management have improved outcomes for malignant variants over recent decades.^[88]

Role in systemic and neurological disorders

The choroid plexus (ChP) plays a critical role in the pathogenesis of hydrocephalus, particularly through dysregulation of cerebrospinal fluid (CSF) production and flow. In inflammatory conditions, such as those following brain infection or injury, ChP epithelial cells release chemokines like CCL2, which recruit CCR2+ macrophages to the ChP stroma, leading to excessive CSF hypersecretion and ventricular enlargement. ^[89] This inflammatory cascade can exacerbate acquired hydrocephalus, where innate immune activation in the ChP disrupts normal CSF homeostasis. ^[90] Additionally, ChP enlargement or hyperplasia can obstruct CSF pathways, contributing to obstructive hydrocephalus, while therapeutic interventions like endoscopic choroid plexus coagulation aim to reduce CSF overproduction by ablating hyperactive epithelial tissue. ^[91] In infectious diseases, the ChP serves as a primary entry point for pathogens into the central nervous system (CNS), facilitating meningitis and ventriculitis. Bacterial agents, such as Escherichia coli in neonatal meningitis, invade ChP epithelial cells via basolateral mechanisms involving virulence factors like S fimbriae, breaching the blood-CSF barrier and allowing bacterial dissemination into the CSF. ^[92] Similarly, Neisseria meningitidis exploits Arp2/3 signaling and dynamin-dependent pathways to traverse the ChP epithelium, triggering ventriculitis and widespread CNS inflammation. ^[93] Viral infections can also compromise ChP integrity, leading to barrier leakage and immune cell infiltration that amplifies meningeal inflammation. ^[94] The ChP contributes to neurodegenerative disorders by impairing waste clearance and promoting protein aggregation. In Alzheimer's disease (AD), ChP dysfunction reduces the clearance of amyloid-β (Aβ) from the CSF via receptors like megalin, resulting in Aβ accumulation and exacerbated neurodegeneration; reduced megalin expression correlates with higher brain Aβ levels in AD patients. ^[95] ^[96] In multiple sclerosis (MS), ChP fibrosis and epithelial thickening, driven by chronic inflammation, disrupt the blood-CSF barrier and facilitate immune cell entry, correlating with lesion burden and disease progression. ^[97] For Parkinson's disease (PD), the ChP may propagate α-synuclein pathology, as seeding-competent α-synuclein in CSF—potentially derived from ChP sources—facilitates its spread across brain regions, contributing to motor deficits. ^[98] Systemic conditions alter ChP structure and function, influencing CNS homeostasis. In diabetes, dysregulation of glucose transport occurs due to impaired insulin signaling and reduced expression of glucose transporters like GLUT1 in ChP epithelium, potentially exacerbating neuroinflammation and cognitive decline. ^[99] Hypertension induces ChP remodeling, including increased calcification and variations in CSF protein composition, which may stem from endothelial dysfunction and heightened vascular permeability. ^[100] During COVID-19 infection, SARS-CoV-2 targets the ChP, causing epithelial damage, barrier disruption, and inflammatory enlargement that persists in long COVID, linking to cognitive impairments. ^[101] ^[102] In autoimmune disorders, the ChP acts as an immune gateway, amplifying CNS involvement. Neuromyelitis optica spectrum disorder (NMOSD) features AQP4 expression on ChP epithelial cells, where anti-AQP4 autoantibodies induce complement activation and barrier pathology, contributing to periventricular inflammation. ^[103] In systemic lupus erythematosus (SLE), particularly neuropsychiatric variants, ChP inflammation—termed choroid plexitis—involves T-cell infiltration and tertiary lymphoid structure formation, driving autoantibody-mediated CNS damage. ^[104] ^[105] Therapeutically, the ChP's relatively permeable barrier offers a route for CNS drug delivery, bypassing the blood-brain barrier via intra-CSF administration or targeted transport across ChP epithelium. ^[106] Experimental approaches, such as selective ChP ablation, have been explored to modulate CSF dynamics in inflammatory conditions, with potential extensions to alleviate neurogenic components of chronic pain by reducing inflammatory signaling from ChP-resident immune cells. ^[107]

History and etymology

Historical perspectives

The discovery of the choroid plexus dates back to ancient times, with the Greek anatomist Herophilus (c. 335–280 BC) providing the first known description, referring to it as the "choroid meninx" in his studies of brain structures conducted in Alexandria. This early observation highlighted its vascular appearance within the brain's ventricular system. In the 1st century AD, Rufus of Ephesus built upon this by coining the term "chorioid," emphasizing its net-like, chorionic quality in his anatomical texts. During the Renaissance, Andreas Vesalius advanced the understanding through detailed illustrations in his seminal work De humani corporis fabrica (1543), depicting the choroid plexus in the lateral, third, and fourth ventricles and noting its role in the ventricular architecture. This visual documentation marked a significant milestone in anatomical accuracy, shifting focus from speculative philosophy to empirical observation. In the 19th century, François Magendie (1825) linked the choroid plexus to cerebrospinal fluid (CSF) dynamics by describing the foramina that allow CSF circulation from the ventricles to the subarachnoid space, establishing its connection to fluid pathways.^[108] The 20th century brought experimental confirmation of the choroid plexus's functions. Harvey Cushing's 1913 studies, involving animal models, definitively identified it as the primary site of CSF production, revolutionizing views on intracranial physiology.^[25] Advancements in electron microscopy during the 1950s, particularly by researchers like Max W. Brightman, revealed the tight junctions in choroid plexus epithelium that form the blood–CSF barrier, preventing unregulated solute passage.^[109] From the 1980s onward, molecular studies identified key transporters, such as Na+/K+-ATPase and carbonic anhydrase, essential for ion and water movement in CSF secretion.^[27] In the modern era, since the 2000s, advanced imaging and genomic approaches have uncovered additional roles, including immune surveillance through transcriptomic profiling that shows expression of cytokines and immune-related genes in choroid plexus tissue.^[110] Research in the 2020s has integrated these findings with the glymphatic system, demonstrating how the choroid plexus facilitates waste clearance and modulates neuroimmune interactions via CSF flow dynamics.^[111]

Etymology

The term "choroid" derives from the Greek words khórion (χόριον), meaning "membrane" or "skin," particularly referring to the fetal membrane or afterbirth, and -eidḗs (-ειδής), a suffix indicating resemblance or likeness.^[112] This combination yields khorioeidḗs (χοριοειδής), translated as "like the chorion," reflecting the structure's vascular, membranous appearance akin to fetal integuments.^[113] The anatomist Galen (2nd century AD) applied "chorion" to describe the chorionic membrane in fetal contexts, influencing its later anatomical usage for brain structures with a similar delicate, vascular quality.^[114] The component "plexus" originates from Latin plexus, the past participle of plectere meaning "to braid" or "to intertwine," denoting a network or interlacing of fibers, nerves, or vessels.^[115] In anatomical nomenclature, it has been employed since the 16th century to describe such braided vascular arrangements, emphasizing the intertwined capillary bed within the structure.^[115] The full Latin term plexus choroideus (or plexus chorioideus) emerged in Renaissance and post-Renaissance anatomy texts to designate the choroid network, combining the Greek-derived "choroideus" with the Latin "plexus" for precision in describing the vascular formation.^[115] This nomenclature transitioned to English as "choroid plexus" by the 18th century, aligning with the era's adoption of Latin-Greek hybrids in medical terminology.^[112] Earlier historical variants include "choroid meninx," coined by Herophilus (c. 335–280 BC) to refer to the inner ventricular lining resembling a vascular membrane.^[116] Additionally, "tela choroidea" denotes the thin, choroid-like web or membrane serving as the plexus's precursor, highlighting its web-like (tela, Latin for "web") and membranous qualities.^[115] In modern usage, the term "choroid plexus" has been standardized through international anatomical nomenclatures, beginning with the Nomina Anatomica adopted at the Basel International Anatomical Congress in 1895, which formalized Latin-based terms for consistency across scientific literature, with no significant alterations since.^[117]

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The anlage of the choroid plexus could be identified on the surface of the everting brain folds as early as gestational day 13. Thus, the abnormal eversion of ...
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Anencephaly and other neural tube defects | MedLink Neurology
Anencephaly is a lethal neural tube defect from incomplete anterior closure, leaving absent cranial vault and cerebral structures.Missing: agenesis | Show results with:agenesis
[13]
Normal growth curve of choroid plexus in children: implications for ...
Sep 8, 2023 · This study provides normal growth curves for intracranial volume, choroid plexus volume, and lateral ventricles volume.Missing: postnatal | Show results with:postnatal
[14]
Choroid plexus–CSF system - Neurology.org
Dec 18, 2015 · The choroid plexus epithelium expressed all the components of the renin-angiotensin system as well as the angiotensin type 1 receptor (AT1).Choroid Plexus--Csf System · Choroid Plexus Epithelium · Csf Secretion
[15]
Assessment of Physiologic Intracranial Calcification in Healthy ...
Feb 1, 2019 · It is most commonly found in the choroid plexus, pineal gland, habenula, and dura matter. It is present in 50%–70% of adults above the age of 30 ...
[16]
Characterization of Age-Related Differences in the Human Choroid ...
Sep 16, 2021 · Functionally, CSF production and turnover decrease with age in the CP (Preston, 2001; Stoquart-ElSankari et al., 2007). Thus, an increase in ...
[17]
Choroid plexus, aging of the brain, and Alzheimer's disease - PubMed
May 1, 2003 · Enzymatic activities of epithelial cells decrease significantly. CSF secretion decreases as much as 50%. These modifications are concurrent ...Missing: production decline
[18]
Cerebrospinal Fluid Pressure Decreases with Older Age - PMC
Dec 26, 2012 · Although opening CSF pressures were similar between the two groups, the mean CSF production was reduced by over 50% in the older age group (0.19 ...
[19]
Proliferation of Cultured Mouse Choroid Plexus Epithelial Cells
We conclude that although CPECs normally have a slow turnover rate, they expand in response to external stimuli such as injury and/or growth factors, which ...
[20]
The Choroid Plexus and Cerebrospinal Fluid: Emerging Roles in ...
Although universally recognized as the source of cerebrospinal fluid (CSF), the choroid plexus (ChP) has been one of the most understudied tissues in ...
[21]
Neuroanatomy, Cerebrospinal Fluid - StatPearls - NCBI Bookshelf
Jul 7, 2025 · The classical theory attributes approximately 80% of CSF production to the choroid plexus and the remaining 20% to secretion by endothelial ...
[22]
Cerebrospinal fluid circulation: What do we know and how do we ...
Apr 18, 2018 · CSF forms at a rate of about 0.3–0.4 mL/min; translating to 18-25 mL/hour and 430–530 mL/day.[1] The classic thought is that CSF flows due to ...
[23]
Molecular Mechanisms of Cerebrospinal Fluid Production - PMC
The epithelial cells of the choroid plexuses secrete cerebrospinal fluid (CSF), by a process which involves the transport of Na+, Cl- and HCO3- from the blood ...
[24]
Cerebrospinal fluid production by the choroid plexus - PubMed Central
Mar 22, 2022 · This review assesses evidence related to CSF secretion and posits that transporters expressed in the CSF-secreting tissue, the choroid plexus, play a central ...
[25]
Low levels of Na, K-ATPase and carbonic anhydrase II during ... - NIH
Low levels of Na, K-ATPase and carbonic anhydrase II during choroid plexus development suggest limited involvement in early CSF secretion. Pia Johansson. Pia ...
[26]
Cotransporter-mediated water transport underlying cerebrospinal ...
The Na+/K+/2Cl− cotransporter (NKCC1) expressed in the luminal membrane of choroid plexus contributes approximately half of the CSF production, via its unusual ...
[27]
Choroid plexus and the blood–cerebrospinal fluid barrier in disease
May 6, 2020 · Hypersecretion of CSF may also be induced by stimulation of glossopharyngeal and vagus ... production in response to hypoxia in the choroid plexus ...
[28]
Effect of vasopressin on production of cerebrospinal fluid - PubMed
The goal of this study was to examine the role of arginine vasopressin in humoral regulation of choroid plexus function. Production of cerebrospinal fluid ...
[29]
Cerebrospinal Fluid Secretion by the Choroid Plexus
Oct 1, 2013 · The choroid plexus epithelium is a cuboidal cell monolayer, which produces the majority of the cerebrospinal fluid. The concerted action of ...
[30]
Day–night fluctuations in choroid plexus transcriptomics and ...
The CSF secretion rate is elevated in the dark phase in both humans and rats, which could support the CSF flow along the paravascular spaces that may be ...
[31]
Nocturnal increase in cerebrospinal fluid secretion as a circadian ...
Jun 23, 2023 · Our findings suggest that CSF dynamics are modulated by the circadian rhythm, rather than merely sleep itself. Supplementary Information. The ...
[32]
Choroid plexus and the blood–cerebrospinal fluid barrier in disease
May 6, 2020 · The choroid plexus (CP) forming the blood–cerebrospinal fluid (B-CSF) barrier is among the least studied structures of the central nervous system (CNS) despite ...
[33]
Claudin-1, claudin-2 and claudin-11 are present in tight junctions of ...
The choroid plexus epithelium forms the blood-cerebrospinal fluid (CSF) barrier and is responsible for the secretion of the CSF from the blood.
[34]
Blood—Cerebrospinal Fluid Barrier - Basic Neurochemistry - NCBI
The major site of CSF formation is the choroid plexus, and from a morphological viewpoint, the epithelial cells of this tissue are similar to other secretory ...
[35]
Blood Cerebrospinal Fluid Barrier - an overview | ScienceDirect Topics
The blood–CSF barrier (BCB) is defined as a choroidal barrier system formed ... molecular weight of less than 500 Daltons (Da).11. View article · Read ...
[36]
Abundant Expression of OCT2, MATE1, OAT1, OAT3, PEPT2, BCRP ...
BCRP, MRP4, OATP2B1, MATE1, and GLUT1 are at the blood-facing membrane, while OAT3, PEPT2, MRP3, OCT2, xCT, MCT1, MCT4, and MCT8 are at the CSF-facing membrane.
[37]
Multidrug resistance protein 1 protects the choroid plexus epithelium ...
Our results indicate that Mrp1 helps to limit tissue distribution of certain drugs and contributes to the blood-CSF drug-permeability barrier. Introduction.Missing: GLUT1 OAT3
[38]
CSF, blood-brain barrier, and brain drug delivery
Areas Covered: Drug distribution into the CSF is a function of drug transport across the choroid plexus, which forms the blood-CSF barrier ... molecular weight.<|control11|><|separator|>
[39]
TNFα Induces Choroid Plexus Epithelial Cell Barrier Alterations by ...
The choroid plexus epithelium constitutes the structural basis of the blood-cerebrospinal fluid barrier. Since the cytokine TNFα is markedly increased ...
[40]
Thyroid hormones and fetal neurological development in
Our review will focus on the ontogeny of thyroid hormone in fetal development, with a focus on cell membrane transporters and TR action in the brain.Ontogenesis Of Thyroid... · Thyroid Hormone Transporters... · Tr Genes And Activity
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Imaging blood-brain barrier dysfunction: A state-of-the-art review ...
When present, disruption of the BBB in WMLs leads to extravasation of gadolinium (Gd) contrast agents seen on T1-weighted MRI, highlighting “active” lesions.
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The immune and metabolic milieu of the choroid plexus as a ...
... cytokines, type-I interferon, and complement components, can perpetuate brain inflammation and cognitive deterioration in aging and neurodegeneration.
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Choroid Plexus in Healthy and Diseased Brain - Oxford Academic
Feb 16, 2016 · The choroid plexus is composed of epithelial cells resting on a basal lamina. These cells produce the cerebrospinal fluid (CSF), which has many functions.
[44]
The choroid plexus and its role in the pathogenesis of neurological ...
Sep 10, 2022 · The choroid plexus (CP) is a highly vascularized complex found within each of the four ventricles of the brain. It is comprised of a monolayer ...
[45]
Macrophages on the margin: choroid plexus immune responses - PMC
Here, we review recent studies on ChP immune cells, with a focus on the ontogeny, development, and behaviors of ChP macrophages.
[46]
Cell trafficking through the choroid plexus - PMC - PubMed Central
It serves as a gateway for immune cell trafficking into the CSF and is in an excellent position to provide continuous immune surveillance by CD4+ T cells, ...Missing: debris | Show results with:debris
[47]
Transport of thyroid hormones via the choroid plexus into the brain
Thyroid hormones enter the choroid plexus via thyroid hormone transmembrane transporters and leave the choroid plexus to enter the cerebrospinal fluid via ...Missing: glucocorticoids | Show results with:glucocorticoids
[48]
Choroid plexus is an additional source of melatonin in the brain
Sep 27, 2018 · Our data show that the CP is a local source of melatonin to the central nervous system, probably contributing to its high levels in the cerebrospinal fluid.
[49]
Differential regulation of leptin transport by the choroid plexus and ...
Our findings suggest a key role of high affinity leptin transporters in the hypothalamus and choroid plexus in regulating leptin entry into the CNS and CSF ...Missing: responsive | Show results with:responsive
[50]
Glymphatic distribution of CSF-derived apoE into brain is isoform ...
Dec 8, 2016 · We show that the glymphatic fluid transporting system contributes to the delivery of choroid plexus/CSF-derived human apoE to neurons.
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Altered clearance of beta-amyloid from the cerebrospinal fluid following subchronic lead exposure in rats: Roles of RAGE and LRP1 in the choroid plexus.
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The path from the choroid plexus to the subventricular zone - Frontiers
Aug 9, 2012 · Wnt signaling regulates symmetry of division of neural stem cells in the adult brain and in response to injury. Stem Cells 29, 528–538.
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Emergence and Developmental Roles of the Cerebrospinal Fluid ...
Feb 10, 2020 · This review examines the current understanding about early CSF and its maturation and roles during CNS development and discusses open questions in the field.
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Glucose, Fructose, and Urate Transporters in the Choroid Plexus ...
Due to the rapid consumption of glucose by brain cells, a downhill gradient of glucose from blood towards the brain ISF is maintained.
[55]
Release of insulin produced by the choroid plexis is regulated by ...
Insulin is expressed and produced in epithelial cells of the choroid plexus and its secretion is regulated by serotonergic activity through 5HT2C receptor.Missing: homeostasis | Show results with:homeostasis
[56]
Transport across the choroid plexus epithelium
The choroid plexus epithelium is a secretory epithelium par excellence. However, this is perhaps not the most prominent reason for the massive interest in ...
[57]
The choroid plexus is an important circadian clock component - Nature
Mar 14, 2018 · We discovered robust circadian gene expression rhythms in the CP using two independent reporters, PER2::LUC and Bmal1-ELuc. We found that ...
[58]
Feeding regime synchronizes circadian clock in choroid plexus
Jun 23, 2025 · We identified mechanisms that can signal to the brain the time of feeding and the associated activity state via resetting of the ChP clock.
[59]
Choroid plexus cyst (antenatal) | Radiology Reference Article
Jul 17, 2025 · Antenatal choroid plexus cysts are benign and are often transient typically resulting in utero from an infolding of the neuroepithelium.Missing: pathogenesis | Show results with:pathogenesis
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Spectrum of Choroid Plexus Lesions in Children | AJR
The choroid plexus begins to differentiate in week 6 of gestation shortly after closure of the neural tube and bulging of the pia mater into the ventricular ...Congenital Disorders · Acquired Disorders · XanthogranulomaMissing: hypoplasia | Show results with:hypoplasia
[61]
Prenatal Diagnosis of Choroid Plexus Cyst: What Next? - PMC
Choroid plexus cysts are identified in approximately 1–2% of fetuses in the second trimester, and they occur equally in male and female fetuses [2]. The real ...Missing: pathogenesis | Show results with:pathogenesis
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Choroid plexus cysts - The Fetal Medicine Foundation
Prevalence: 1 in 50 fetuses at 20 weeks' gestation. More than 90% resolve by 26 weeks. ; Ultrasound diagnosis: Single or multiple cystic areas (>2 mm in diameter ...Missing: pathogenesis | Show results with:pathogenesis<|control11|><|separator|>
[63]
Clinical significance of fetal choroid plexus cysts - ScienceDirect.com
Choroid plexus (CP) cysts are commonly detected on routine mid-trimester ultrasound scan. When associated anomalies are detected, the risk is sufficient to ...Missing: prevalence | Show results with:prevalence
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Choroid Plexus Cysts
13 Approximately three fourths of abnormal fetal karyotypes associated with choroid plexus cysts are trisomy 18 and one fourth are trisomy 21.Missing: congenital pathogenesis
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FAQ: Choroid Plexus Cysts | Patient Education - UCSF Health
However, in a very small percentage of fetuses with choroid plexus cysts, there is an associated chromosome disorder called trisomy 18. Fetuses with trisomy 18 ...
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Choroid Plexus Cyst - ISUOG
Jan 11, 2019 · An isolated finding of a choroid plexus cyst does not alter the management of pregnancy. Most of the cysts resolve by 28 weeks. What does it ...
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Perinatal (fetal and neonatal) choroid plexus tumors: a review
Results: Choroid plexus papilloma (CPP) is the most common tumor followed by choroid plexus carcinoma (CPC) and atypical choroid plexus papilloma (ACPP).
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Holoprosencephaly: Review of Embryology, Clinical Phenotypes ...
Mar 30, 2023 · Genetic causes of HPE include chromosomal abnormalities and single gene disorders. Individuals with syndromic forms of HPE (i.e., associated ...
[69]
The 2021 WHO Classification of Tumors of the Central Nervous ...
Jun 29, 2021 · Designating this tumor as CNS WHO grade 4, and therefore equivalent to many untreatable pediatric brain tumors with a dismal outcome, ...
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Choroid Plexus Tumor: Diagnosis and Treatment - NCI
Aug 20, 2024 · Choroid plexus tumors are grouped in three grades based on their characteristics: grade 1, 2, or 3 (also written as grade I, II, or III). Grade ...
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Choroid plexus neoplasms | Radiology Reference Article
Feb 13, 2025 · primary tumors. choroid plexus papilloma (WHO grade I or II "atypical"); choroid plexus carcinoma (WHO Grade III); choroid plexus ...
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Incidence and survival of choroid plexus tumors in the United States
While rare, adult cases of CPT do occur, particularly among patients with CPP, who experienced an AAIR of 0.03 per 100 000 from 2004 to 2017 for cases those ...Abstract · Methods · Results · Discussion
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Choroid Plexus - American Brain Tumor Association | Learn More
They are more common in early infancy and represent over 10% of brain tumors diagnosed in the first year of life. Choroid plexus tumors are even rarer in adults ...
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TP53 Alterations Determine Clinical Subgroups and Survival of ...
Mar 22, 2010 · Choroid plexus carcinomas are pediatric tumors with poor survival rates and a strong, but poorly understood, association with Li-Fraumeni syndrome (LFS).
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Choroid Plexus Papilloma - Medscape Reference
Jun 8, 2023 · Choroid plexus papillomas are rare, accounting for about 1% of all brain tumors, 2-6% of pediatric brain tumors, and 0.5% of adult brain tumors.
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Choroid Plexus Carcinoma - Allen Press
Aug 1, 2008 · Choroid plexus carcinoma is a WHO grade III tumor which is distinguished histologically from CPP based on increased nuclear to cytoplasmic ...
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Choroid plexus tumors (papilloma, atypical papilloma, carcinoma)
Aug 9, 2023 · TP53 sequencing and testing for germ line TP53 mutation is advisable in children with choroid plexus carcinoma. Molecular / cytogenetics images.
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Choroid Plexus Carcinoma: Symptoms, Treatment & Prognosis
Nov 1, 2024 · Choroid plexus carcinoma is a rare, aggressive brain cancer that most often affects infants and children. Treatments include surgery to remove the tumor.
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Choroid plexus papilloma | Radiology Reference Article
Oct 25, 2025 · Choroid plexus papillomas are an uncommon, benign (CNS WHO grade 1) neuroepithelial intraventricular tumor, which can occur in both the ...Choroid plexus carcinoma · Legacy Case · Case · Question 527Missing: congenital | Show results with:congenital
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Feb 4, 2025 · Choroid plexus carcinoma can happen at any age. This brain cancer happens most often in children under 2 years old. Inherited syndromes. Some ...<|separator|>
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Management of choroid plexus tumors—an institutional experience
Feb 19, 2019 · Choroid plexus tumors are rare entities. Resection is the mainstay of treatment in grade I and grade II tumors and adjuvant treatment is usually reserved for ...
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Choroid Plexus Tumors - UCSF Benioff Children's Hospitals
Choroid plexus tumors are rare growths of cells that form in the choroid plexus, a vascular structure inside the brain's ventricles.
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POMS: DI 23022.938 - Choroid Plexus Carcinoma - Social Security
Aug 11, 2021 · Choroid Plexus Carcinoma tumors spread aggressively and prognosis is generally poor. Only about one in four children will survive five years ...<|control11|><|separator|>
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Choroid plexus CCL2‒CCR2 signaling orchestrates macrophage ...
Jun 26, 2024 · We identify the chemokine CCL2, released by ChP epithelial cells, recruits CCR2 + monocytes to the ChP thereby inciting hydrocephalus pathogenesis.
[85]
The choroid plexus links innate immunity to CSF dysregulation in ...
The ChP is also the blood-CSF barrier, gating circulating immune cell entry into the CSF in the setting of infection or tissue damage. The ChP's location at the ...<|separator|>
[86]
Symptomatic obstructive hydrocephalus caused by choroid plexus ...
Oct 2, 2023 · Choroid plexus hyperplasia has been described as a rare cause of communicating hydrocephalus due to cerebrospinal fluid (CSF) overproduction.
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Virulence factor-dependent basolateral invasion of choroid plexus ...
Escherichia coli is the most common Gram-negative causative agent of neonatal meningitis and E. coli meningitis is associated with high morbidity and mortality.
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Invasion of the choroid plexus epithelium by Neisseria meningitidis ...
Sep 6, 2021 · Invasion of the choroid plexus epithelium by Neisseria meningitidis is differently mediated by Arp2/3 signaling and possibly by dynamin ...
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The choroid plexus—a multi-role player during infectious diseases ...
The choroid plexus (CP) is the source of cerebrospinal fluid (CSF) production and location of the blood-CSF barrier (BCSFB), which is constituted by the ...
[90]
Clearance of amyloid-β peptide across the choroid plexus ... - PubMed
Patients with AD have reduced levels of megalin at the choroid plexus, which in turn seem to increase brain levels of Aβ through a decreased efflux of brain Aβ.
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The Choroid Plexus Removes β-Amyloid from Brain Cerebrospinal ...
... 3000 daltons mol wt cutoff membrane (14,000 g, 30 mins, 4°C). Medium ... surface area; CDonor, the initial concentration in the donor chamber; and δC ...
[92]
The Time Trajectory of Choroid Plexus Enlargement in Multiple ...
Apr 1, 2024 · Choroid plexus (CP) can be seen as a watchtower of the central nervous system (CNS) that actively regulates CNS homeostasis.
[93]
The Spreading and Effects of Human Recombinant α-Synuclein ...
Mar 1, 2024 · Furthermore, we identify the choroid plexus (ChP), an often-neglected brain region, as a potentially important player in PD pathology due to its ...
[94]
Metabolic Alterations Associated to Brain Dysfunction in Diabetes
Accordingly, decrease in insulin receptor levels and impaired insulin signalling was observed in the hippocampus, cortex and choroid plexus [62], and insulin ...
[95]
High Blood Pressure Effects on the Blood to Cerebrospinal Fluid ...
The conclusion made here is that hypertension in SHR produces important variations in cerebrospinal fluid proteins that could be due to a choroid plexus ...
[96]
SARS-CoV-2 Infects the Brain Choroid Plexus and Disrupts the ...
Oct 13, 2020 · We show that infection with SARS-CoV-2 damages the choroid plexus epithelium, leading to leakage across this important barrier that normally prevents entry of ...
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SARS-CoV-2 induces blood-brain barrier and choroid plexus barrier ...
SARS-CoV-2 induces blood-brain barrier and choroid plexus barrier impairments and vascular inflammation in mice
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Pathogenic implications of cerebrospinal fluid barrier pathology in ...
Feb 9, 2017 · Within the choroid plexus, AQP4 loss was coincident with C9neo immunoreactivity on epithelial cell membranes only in NMO cases. These ...
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Tertiary lymphoid structures in the choroid plexus ... - PubMed Central
Jun 6, 2019 · Tertiary lymphoid structures are found in the choroid plexus of a mouse model of lupus with neuropsychiatric disease, suggesting a mechanism of ...Missing: plexitis | Show results with:plexitis
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Anti-intercellular adhesion molecule-1 (ICAM-1) antibody ... - PubMed
Brain histology revealed a similar degree of choroid plexus inflammation in both groups. Our study demonstrated that anti-ICAM-1 was effective in ...
[101]
Recent advances in drug delivery and targeting to the brain - PMC
For instance, drug delivery from the blood into the CSF via the choroid plexus is comparatively simpler, providing a considerably leakier barrier than the BBB.
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Targeting choroid plexus epithelium as a novel therapeutic strategy ...
Jun 17, 2022 · It is now believed that the choroid plexus is in an inflammatory state after damage to the brain. This state, along with changes in the cilia, ...
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Magendie and Luschka: Holes in the 4th ventricle - PMC - NIH
Hubert von Luschka (1820-1875) (Figure 2) was a German anatomist. In his book "The choroid plexuses of the human brain" (Die Adergeflechte des menschlichen ...Missing: Goodsir 1845
[104]
THE ELECTRON MICROSCOPY OF THE CHOROID PLEXUS
Oct 24, 2025 · By the mid-1950's, TEM methods had improved considerably and were increasingly used by numerous research groups for detailed studies of choroid ...
[105]
Transcriptome sequencing of the choroid plexus in schizophrenia
Nov 29, 2016 · The choroid plexus (CP) has a key role in maintaining brain homeostasis by producing cerebrospinal fluid (CSF), by mediating transport of ...
[106]
Multimodal MRI reveals impaired glymphatic function with choroid ...
Aug 19, 2025 · This study evaluated CSF circulation in patients with AD using magnetic resonance imaging (MRI)-derived measures, including choroid plexus (CP) ...Missing: 2020s | Show results with:2020s
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Choroid - Etymology, Origin & Meaning
From Greek khorion (membrane) + eidos (resemblance), this 1680s term means "like a chorion," describing a membranous structure. Origin reflects its meaning.Missing: plexus anatomical Galen Herophilus
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Choroid plexuses - Clinical Anatomy Associates Inc.
Jun 5, 2015 · The suffix [-oid] means "similar to", while the root term [chor-] derives from the Greek word [χορίου] pronounced (joríu), meaning "dermis", " ...Missing: Galen Herophilus<|control11|><|separator|>
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How the brain got its names and numbers.
Sixteenth century anatomists, including. Vesalius, shifted some attention toward the cor- tex, but even then, and for the next two centuries, central brain ...
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Use and meaning of the anatomical terms „Plexus choroideus” and ...
From an etymological point of view, “plexus” means braid or plexus, in anatomy an interlacing of nerves, vessels, or fibres [102].Missing: Greek Galen
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The Neuroanatomy of Herophilus - ResearchGate
Aug 10, 2025 · He reported ''the tunic covering the ventricles of the brain on the inside'' and called it ''choroid meninx'' [1, 30] , but the latter ...
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The standard anatomical position was abandoned and the terms of direction were related to parts of the body, making the terms applicable to all vertebrates ...<|control11|><|separator|>