Fact-checked by Grok 2 weeks ago

LRP5

LRP5 is a gene located on chromosome 11q13.2 that encodes low-density lipoprotein receptor-related protein 5 (LRP5), a 1,615-amino acid transmembrane co-receptor essential for canonical Wnt/β-catenin signaling.^[1]^[2] This protein facilitates the binding of Wnt ligands to Frizzled receptors on the cell surface, stabilizing β-catenin and promoting its nuclear translocation to regulate genes involved in cell proliferation, differentiation, migration, and survival.^[2] LRP5 is widely expressed across tissues, with prominent roles in osteoblasts for bone homeostasis, retinal vascularization for eye development, and additional functions in cholesterol metabolism, glucose-induced insulin secretion, and adipocyte insulin sensitivity.^[1]^[2]^[3] In bone physiology, LRP5 primarily acts within the osteoblast lineage to control proliferation and inhibit apoptosis, thereby influencing bone mass accrual and density.^[4] Its activity is negatively regulated by secreted antagonists such as dickkopf-1 (DKK1) and sclerostin (SOST), which bind to LRP5 and prevent Wnt signal transduction.^[2] Beyond skeletal effects, LRP5 contributes to the development of retinal and inner ear blood vessels, as well as systemic metabolic processes, including the modulation of serotonin synthesis in the gut that indirectly affects bone formation.^[1]^[2] Dysregulation of LRP5 signaling disrupts these pathways, leading to a spectrum of developmental and metabolic disorders. Mutations in LRP5 are associated with contrasting bone phenotypes depending on their functional impact. Loss-of-function variants, such as nonsense mutations (e.g., W10X, R428X), cause osteoporosis-pseudoglioma syndrome (OPPG; OMIM 259770), a rare autosomal recessive disorder featuring juvenile-onset osteoporosis, low bone mineral density, and ocular abnormalities like pseudoglioma due to impaired retinal vascularization.^[2] These mutations also underlie familial exudative vitreoretinopathy type 4 (EVR4; OMIM 601813) and LRP5-related primary osteoporosis, both involving reduced Wnt signaling and defective tissue development.^[1]^[2] In contrast, gain-of-function mutations, notably G171V in the first β-propeller domain, result in autosomal dominant high bone mass traits (OMIM 601884), including osteosclerosis and endosteal hyperostosis, where enhanced Wnt activity leads to increased bone density without major adverse effects.^[2] Additional LRP5 variants have been linked to anophthalmia/microphthalmia and polycystic liver disease type 4 (PCLD4; OMIM 617875), highlighting its broader role in organogenesis and disease.^[1]^[2] Research on LRP5 has advanced understanding of Wnt pathway therapeutics, with inhibitors of its antagonists (e.g., anti-sclerostin antibodies) approved for osteoporosis treatment, underscoring the protein's therapeutic potential.^[4] Animal models, including Lrp5-knockout mice exhibiting low bone mass and retinal defects, further validate its conserved functions across species.^[2] Ongoing studies continue to explore LRP5's implications in metabolic syndromes, such as its promotion of lower-body fat distribution and insulin sensitivity in adipocytes.^[5]

Genetics

Genomic Location and Organization

The LRP5 gene is located on the long (q) arm of human chromosome 11 at cytogenetic band 11q13.2, spanning approximately 137 kb from genomic coordinates 68,312,447 to 68,449,275 on the GRCh38.p14 assembly.^[6] This positioning places it within a region associated with various genetic linkages in bone-related disorders. Orthologs of LRP5 are conserved in other vertebrates, including the mouse Lrp5 gene on chromosome 19, reflecting shared genomic architecture across mammals.^[7] The canonical transcript comprises 23 exons that collectively encode a 1,615-amino-acid protein, with UTRs in the first and last exons. The gene model includes 28 unique exons across alternative transcripts.^[8] Intron-exon boundaries are precisely defined, facilitating accurate splicing; for instance, studies of splicing mutations have mapped critical junctions, such as those at exons 7 and 20, where disruptions can alter transcript integrity. Alternative splicing generates at least 15 distinct transcripts, allowing for potential isoform diversity in different tissues or conditions.^[6]^[9] Evolutionary analyses highlight the conservation of LRP5 across species, with 201 orthologs identified, underscoring the preservation of essential regulatory and structural elements. A 2024 study revealed archaic human variants, including five missense mutations (e.g., p.A67T and p.A67V) in Neanderthals and Denisovans located in the first β-propeller domain, which enhance Wnt pathway activation and correlate with elevated bone mineral density—contrasting with modern human alleles that may contribute to relatively lower skeletal robustness as an adaptation.^[6]^[10]

Transcription and Regulation

Transcription of the LRP5 gene produces multiple mRNA isoforms through alternative splicing, with at least 15 distinct transcripts widely expressed across human tissues, with particularly high levels observed in the liver, heart, lung, pancreas, skeletal muscle, kidney, and adipose tissue.^[11] Notable expression also occurs in bone-forming cells such as osteoblasts, the retina of the eye, and regions of the central nervous system including the brain, where LRP5 contributes to developmental processes.^[11] These tissue-specific patterns underscore LRP5's role in diverse physiological contexts, though quantitative RNA levels vary, with lower baseline expression reported in brain tissue compared to visceral organs. The promoter region of LRP5 contains genetic variations that influence transcriptional activity, including polymorphisms associated with bone mineral density in young women, indicating regulatory elements responsive to environmental and genetic factors.^[12] Epigenetic mechanisms contribute to LRP5 regulation, with DNA methylation at the promoter region identified as a key modulator in specific contexts. For instance, altered methylation patterns in the LRP5 promoter have been linked to metabolic perturbations in offspring of sleep-deprived fathers, affecting pancreatic islet function and Wnt signaling components.^[13] Recent studies highlight such methylation changes as part of broader epigenetic responses to environmental stressors.^[14] Post-transcriptional regulation of LRP5 mRNA occurs through microRNAs (miRNAs) that bind to its 3' untranslated region, suppressing translation and promoting degradation. The miR-23a miRNA directly targets LRP5, inhibiting its expression and thereby attenuating osteogenic differentiation of human bone marrow mesenchymal stem cells by dampening Wnt signaling.^[15] Similarly, miR-375-3p targets LRP5 to negatively regulate osteogenesis, reducing β-catenin levels and bone formation.^[16] The miR-29 family, while not directly targeting LRP5, indirectly influences its pathway by promoting Wnt/β-catenin activity in osteoblasts through feedback loops that enhance overall bone anabolic processes.^[17]

Protein

Structure

LRP5 is a single-pass type I transmembrane protein characterized by a large extracellular domain, a hydrophobic transmembrane helix spanning approximately 20-25 amino acids, and a short intracellular C-terminal tail of about 216 residues. The extracellular domain, which constitutes the majority of the protein's length, features a modular architecture typical of the low-density lipoprotein receptor family: it begins with four N-terminal low-density lipoprotein receptor class A (LDL-A) repeats, followed by four tandem β-propeller/EGF-like modules—each module consisting of six YWTD repeats that fold into a six-bladed β-propeller structure connected to an epidermal growth factor (EGF)-like domain—and terminates with three additional LDL-A repeats.^[18]^[19] The LDL-A repeats, rich in cysteine residues and stabilized by disulfide bonds, primarily mediate initial ligand binding through calcium-dependent interactions, while the β-propeller domains, formed by the YWTD motifs, provide structural rigidity and contribute to ligand specificity by forming funnel-like pockets for selective engagement.^[20] The EGF-like domains, in turn, link the propeller modules and may influence overall domain flexibility. Cryo-electron microscopy (cryo-EM) studies in the 2020s, particularly on the closely related LRP6 homolog, have provided high-resolution insights (around 3.8 Å) into the extracellular domain's conformation within signaling complexes, revealing a compact arrangement of the β-propeller modules that facilitates Wnt-Frizzled interactions.^[21] The full-length LRP5 polypeptide comprises 1,615 amino acids with a calculated molecular mass of approximately 179 kDa; however, extensive post-translational glycosylation at multiple N-linked sites (at least six predicted) increases the observed molecular weight to 180-200 kDa in SDS-PAGE analyses.^[2]^[22]

Post-Translational Modifications

LRP5 undergoes N-linked glycosylation at multiple asparagine residues within its extracellular domains, which is critical for proper protein folding, stability, and trafficking to the plasma membrane. The extracellular domain contains six predicted N-linked glycosylation sites, and dysregulation of this modification in the endoplasmic reticulum can impair LRP5/6 transport, thereby attenuating Wnt signaling responsiveness.^[23] Phosphorylation occurs primarily in the cytoplasmic tail of LRP5, with key sites including five PPPSP motifs targeted by glycogen synthase kinase 3β (GSK3β) upon Wnt stimulation. These phosphorylation events create docking sites for scaffold proteins like AXIN, thereby inhibiting the β-catenin destruction complex and promoting canonical Wnt pathway activation.^[24]^[25]^[22] Ubiquitination regulates LRP5 stability and turnover by targeting it for endocytosis, a process modulated through binding of AXIN to the phosphorylated cytoplasmic tail. E3 ubiquitin ligases facilitate this modification, leading to internalization of the LRP5-Frizzled-Wnt complex and fine-tuning signal duration to prevent excessive pathway activation.^[26]^[27]

Function

Role in Wnt Signaling

LRP5 functions as an essential co-receptor in the canonical Wnt/β-catenin signaling pathway, partnering with Frizzled (FZD) family receptors to transduce extracellular Wnt signals into intracellular responses. Upon binding of Wnt ligands to both FZD and LRP5 on the cell surface, a ternary complex forms that facilitates the recruitment of the cytoplasmic adaptor protein Dishevelled (DVL). This interaction promotes the phosphorylation of LRP5's intracellular domain by kinases such as GSK3β and CK1, creating binding sites for AXIN and inhibiting the β-catenin destruction complex.^[25] The β-catenin destruction complex, comprising AXIN, APC, GSK3β, and CK1, normally phosphorylates β-catenin, marking it for ubiquitination and proteasomal degradation. In the presence of the Wnt-LRP5-FZD ternary complex, DVL recruitment disrupts this complex by sequestering AXIN to the plasma membrane, thereby preventing β-catenin phosphorylation and allowing its accumulation in the cytoplasm. Stabilized β-catenin then translocates to the nucleus, where it interacts with TCF/LEF transcription factors to activate target gene expression. This signal transduction mechanism underscores LRP5's central role in canonical Wnt pathway activation.^[28] Canonical Wnt signaling via LRP5 is negatively regulated by secreted antagonists such as Dickkopf-1 (DKK1), which binds with high affinity to the first β-propeller domain of LRP5's extracellular region. This binding disrupts the formation of the Wnt-FZD-LRP5 ternary complex and promotes the internalization of LRP5, thereby inhibiting downstream β-catenin stabilization.^[29] Although LRP5 is predominantly involved in the canonical pathway, emerging evidence suggests minor contributions to non-canonical Wnt signaling, such as modulation of planar cell polarity or Wnt/Ca²⁺ pathways in specific contexts, though these roles are secondary and less characterized compared to its canonical functions.^[30]

Regulation of Bone Homeostasis

LRP5 serves as a co-receptor in the canonical Wnt/β-catenin signaling pathway, playing a pivotal role in promoting osteoblast proliferation and differentiation within bone tissue. Activation of LRP5 by Wnt ligands stabilizes β-catenin, which translocates to the nucleus to induce transcription of genes essential for osteoblast maturation, such as Runx2 and Osterix.^[31] Studies in Lrp5 knockout mice demonstrate reduced osteoblast numbers and impaired bone formation, underscoring LRP5's necessity for maintaining osteoblast activity during bone accrual.^[32] Furthermore, LRP5-mediated Wnt signaling enhances osteoblast survival and mineralization, contributing to overall bone mass regulation.^[4] In addition to direct effects on osteoblasts, LRP5 indirectly inhibits osteoclast activity by modulating the RANKL/OPG axis in bone cells. Wnt signaling through LRP5 upregulates osteoprotegerin (OPG) expression while suppressing receptor activator of nuclear factor kappa-B ligand (RANKL), thereby reducing osteoclast differentiation and bone resorption.^[33] This balance is evident in models where LRP5 loss leads to elevated RANKL/OPG ratios and increased osteoclastogenesis, resulting in net bone loss.^[4] Consequently, LRP5 helps preserve bone homeostasis by favoring formation over resorption. LRP5 also integrates with the BMP pathway to support fracture healing, where BMP-2 induces Lrp5 expression to amplify Wnt/β-catenin signaling and promote osteogenic repair.^[34] This crosstalk enhances mesenchymal stem cell commitment to osteoblasts at fracture sites, accelerating callus formation and bone regeneration.^[35] In LRP5-deficient models, delayed fracture healing highlights its role in coordinating these pathways for effective skeletal repair.^[36]

Interactions

Protein-Protein Interactions

LRP5 serves as a co-receptor in the Wnt signaling pathway by binding to members of the Frizzled (FZD) receptor family, specifically FZD1 through FZD10, to form a heteromeric complex essential for signal transduction.^[37] This interaction occurs independently of Wnt ligands and is regulated by phosphorylation events that stabilize the receptor complex on the cell surface.^[38] Structural studies have shown that the extracellular domains of LRP5 directly contact the cysteine-rich domain of Frizzled receptors, facilitating their clustering and activation.^[39] In the cytoplasmic domain, LRP5 interacts with Axin and Dishevelled (DVL) proteins to promote β-catenin stabilization. LRP5 binds directly to the N-terminal region of Axin, recruiting it to the plasma membrane and leading to the disassembly of the β-catenin destruction complex.^[40] Concurrently, LRP5, in coordination with DVL proteins, promotes Axin recruitment and phosphorylation, inhibiting GSK3β-mediated β-catenin degradation, thereby allowing β-catenin accumulation and nuclear translocation.^[41] These interactions are critical for the signalosome formation observed in canonical Wnt pathway activation.^[42] LRP5 also associates with its structural homolog LRP6 to form heterodimers that amplify Wnt signaling efficiency. This heterodimerization occurs via the extracellular β-propeller domains and enhances receptor clustering compared to LRP5 or LRP6 homodimers alone.^[43] In cellular assays, co-expression of LRP5 and LRP6 results in synergistic activation of downstream reporters, underscoring their cooperative role in pathway potentiation.^[44] Additionally, LRP5 forms complexes with GPR124 and RECK in response to Wnt7a, facilitating signaling in central nervous system vascular development.^[45]

Ligand Binding

LRP5, a coreceptor in the canonical Wnt signaling pathway, binds various Wnt ligands through its extracellular domain, which consists of four β-propeller modules (E1–E4) followed by LDL receptor-like repeats. Canonical Wnt ligands such as Wnt1, Wnt3a, and Wnt10b interact with these domains to initiate signaling, with binding affinities typically in the low nanomolar range. For instance, Wnt3a exhibits a dissociation constant (Kd) of approximately 9 nM to the E1E4 fragment of the homologous LRP6 extracellular domain, reflecting similar high-affinity interactions expected for LRP5 due to their 70% sequence identity.^[46] Wnt1 and Wnt10b demonstrate a preference for LRP5 involvement, as their signaling requires both LRP5 and LRP6 at endogenous expression levels in cells like mammary epithelial cells and fibroblasts, whereas Wnt3a signals predominantly through LRP6 alone.^[47]^[48] Antagonists like Dickkopf-1 (DKK1) and sclerostin (SOST) inhibit Wnt binding to LRP5 by directly interacting with its extracellular propeller domains. DKK1 binds bivalently to the first (E1E2) and third (E3E4) propeller domains of LRP5/6, with reported Kd values of around 20–60 nM, effectively blocking Wnt association and promoting receptor endocytosis; this inhibitory mechanism requires co-binding to KREMEN1, which facilitates LRP5 internalization.^[46] SOST primarily targets the first propeller domain (E1) of LRP5, preventing Wnt ligand access and canonical signaling activation in osteoblasts, with high-affinity binding that is reduced in high bone mass-associated LRP5 mutants.^[49] Recent crystallographic studies in the 2020s have elucidated the structural basis of these interactions, primarily using LRP6 as a model due to its homology with LRP5. For example, the 2020 crystal structure of the SOST-LRP6 complex revealed tandem binding sites on the E1 and E2 domains, enhancing inhibitory potency by sterically occluding Wnt access.^[50] Similarly, a 2023 cryo-EM structure of the Wnt-Frizzled-LRP6 initiation complex highlighted modular linker regions in Wnt ligands that dictate specificity for LRP5/6 propeller domains, providing insights into how LRP5 accommodates Wnt1 and Wnt10b through cooperative binding with Frizzled receptors.^[51] These structures underscore the dynamic, multi-site nature of ligand engagement on LRP5, enabling fine-tuned regulation of Wnt signaling.

Clinical Significance

Loss-of-Function Mutations

Loss-of-function mutations in the LRP5 gene, which encodes a co-receptor in the Wnt signaling pathway, lead to reduced protein function and are primarily associated with osteoporosis-pseudoglioma syndrome (OPPG; OMIM 259770), a rare autosomal recessive disorder characterized by severe early-onset osteoporosis and visual impairment due to pseudoglioma-like retinal changes.^[52] These mutations disrupt normal bone formation and retinal vascular development by impairing Wnt signal transduction, resulting in low bone mineral density and increased fracture risk from infancy, alongside leukocoria and eventual blindness.^[52] OPPG has a low prevalence, estimated at fewer than 1 in 1,000,000 individuals worldwide, with most cases reported in consanguineous families, reflecting its recessive inheritance pattern where affected individuals are homozygous or compound heterozygous for pathogenic variants.^[53] Pathogenic variants in LRP5 for OPPG include a variety of loss-of-function types, such as nonsense mutations (e.g., W10X [c.29G>A] and Q853X [c.2557C>T]), which introduce premature stop codons leading to truncated or absent protein via nonsense-mediated decay; frameshift mutations (e.g., T1268fsX1438 [c.3804delA]), which alter the reading frame and produce nonfunctional proteins; and certain missense mutations (e.g., T244M [c.731C>T] and S356L [c.1067C>T]), which impair receptor trafficking or ligand binding as demonstrated by reduced Wnt signaling in functional assays.^[52] Over 40 such mutations have been identified across multiple families, with a mutation detection rate of approximately 70% in clinically diagnosed OPPG cases, highlighting LRP5 as the primary genetic cause.^[52] Heterozygous loss-of-function mutations in LRP5 also cause juvenile primary osteoporosis (OMIM 239800), featuring reduced bone mass and increased childhood fracture risk without ocular abnormalities.^[54] Beyond OPPG, loss-of-function LRP5 mutations are implicated in familial exudative vitreoretinopathy (FEVR), a hereditary retinal vascular disorder featuring peripheral avascular retina, neovascularization, and potential tractional retinal detachment, often presenting in infancy.^[55] A 2025 cohort study of infants with FEVR phenotype reported LRP5 mutations in 33.3% of genetically confirmed cases, underscoring its significant contribution to this condition, particularly in autosomal dominant or recessive forms depending on variant zygosity.^[56] The underlying mechanism involves defective Wnt/β-catenin signaling due to impaired LRP5 interaction with ligands like Wnt proteins or Norrin, leading to diminished β-catenin stabilization and target gene transcription essential for osteoblast proliferation and retinal endothelial cell migration.^[52] In bone, this manifests as reduced osteoblast activity and low bone density, while in the retina, it causes delayed vascularization and abnormal vessel growth, contributing to the vitreoretinopathy observed in both OPPG and isolated FEVR.^[57] Diagnostic criteria for OPPG typically include clinical evidence of juvenile osteoporosis (e.g., fractures before age 5, bone mineral density Z-score ≤ -2.5) combined with ocular findings (e.g., bilateral leukocoria or retinal vascular leakage on fluorescein angiography), confirmed by bidirectional Sanger sequencing or next-generation sequencing of LRP5 revealing biallelic loss-of-function variants.^[52] For FEVR, diagnosis relies on characteristic retinal peripheral non-perfusion on wide-field imaging plus genetic testing, with LRP5 variants supporting classification in up to one-third of pediatric cases.^[56] Additionally, certain heterozygous variants in LRP5 are linked to polycystic liver disease type 4 (PCLD4; OMIM 617875), characterized by multiple benign liver cysts originating from biliary epithelium, typically without kidney cysts.^[58]

Gain-of-Function Mutations

Gain-of-function mutations in the LRP5 gene lead to autosomal dominant disorders characterized by increased bone mineral density (BMD) and hyperostosis, primarily through enhanced canonical Wnt signaling in osteoblasts.^[59] These mutations, often missense variants in the first β-propeller domain of LRP5, result in high bone mass (HBM; OMIM 601884), a condition first identified in families with exceptionally dense bones resistant to fractures.^[60] Representative examples include the G171V mutation, which was the first reported and causes lifelong accumulation of dense cortical and trabecular bone without impairing skeletal function.^[59] Certain gain-of-function variants also underlie Worth syndrome (autosomal dominant endosteal hyperostosis; OMIM 144750), featuring progressive endosteal thickening of long bones, widened mandible, and torus palatinus, but typically sparing the skull base.^[61] For instance, mutations such as p.Gly171Arg (rs121908669) have been linked to HBM phenotypes with variable expressivity, including elevated BMD in the lumbar spine and hips.^[62] A 2025 case report identified a novel heterozygous LRP5 mutation (p.Met282Val) causing endosteal hyperostosis (Worth syndrome) with torus palatinus and mandibular broadening, in the absence of ANKH or SOST involvement, highlighting the spectrum of LRP5-related sclerosing dysplasias.^[63] The molecular mechanism involves reduced inhibition of LRP5 by antagonists like Dickkopf-1 (DKK1) and sclerostin (SOST), leading to constitutively active Wnt/β-catenin signaling that promotes osteoblast proliferation and bone formation.^[64] Specifically, mutations like G171V alter the LRP5 extracellular domain, impairing DKK1 binding and thereby preventing its sequestration of LRP5 from the Wnt-Frizzled complex, resulting in hyperactivation targeted to bone cells.^[65] This resistance to negative regulation contrasts with physiological Wnt modulation and drives the anabolic effects on bone homeostasis.^[66] Clinically, affected individuals exhibit markedly increased BMD (often 2-3 standard deviations above normal), resistance to osteoporosis, and occasional extracranial manifestations such as enlarged jaw or palate tori, with rare progression to facial nerve entrapment causing hearing loss or facial palsy due to foraminal narrowing.^[59] Inheritance is autosomal dominant with high penetrance, though phenotypic severity varies; no increased fracture risk is observed, and management focuses on monitoring for neurologic complications rather than bone-targeted therapies.^[67]

References

[1]
LRP5 gene: MedlinePlus Genetics
### Summary of LRP5 Gene
[2]
603506 - LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED ...
... Lrp5 gene to chromosome 19, which shows homology of synteny with human 11q13. Chen et al. (1999) mapped the human LRP5 gene to 11q13.4 by FISH and between ...
[3]
Low-density lipoprotein receptor-related protein 5 (LRP5) is ... - NIH
Low-density lipoprotein receptor-related protein 5 (LRP5) is essential for normal cholesterol metabolism and glucose-induced insulin secretion.
[4]
LRP5 and bone mass regulation: Where are we now? - PMC
Collectively, these mouse studies suggest that Lrp5 functions in the osteoblast lineage of cells to control proliferation and apoptosis, but has little or no ...
[5]
LRP5 promotes adipose progenitor cell fitness and adipocyte insulin ...
Feb 25, 2025 · Here we show that LRP5 promotes lower-body fat distribution and enhances systemic and adipocyte insulin sensitivity through cell-autonomous ...
[6]
https://www.ensembl.org/Homo_sapiens/Gene/Summary?db=core;g=ENSG00000162337
[7]
MGI:1278315 - low density lipoprotein receptor-related protein 5
View mouse Lrp5 Chr19:3634828-3736564 with: phenotypes, sequences, polymorphisms, proteins, references, function, expression.
[8]
LRP5 LDL receptor related protein 5 [ (human)] - NCBI
Sep 27, 2025 · This gene encodes a transmembrane low-density lipoprotein receptor that binds and internalizes ligands in the process of receptor-mediated ...
[9]
Novel mutations affecting LRP5 splicing in patients with ... - Nature
The LRP5 gene consists of 23 coding exons and is expressed in many tissues. ... PCR amplification products of all 23 coding exons and exon–intron boundaries of ...
[10]
Evolutionary and functional analyses of LRP5 in archaic and extant ...
May 27, 2024 · We have analyzed the LRP5 gene, which is known to be associated with high bone mineral density conditions, from an evolutionary and functional point of view.
[11]
LRP5: A Multifaceted Co-Receptor in Development, Disease, and ...
Beyond the skeletal system, LRP5 has emerged as a key regulator of retinal angiogenesis, vascular integrity, renal tubular function, neurodevelopment, and lipid ...
[12]
Association of low-density lipoprotein receptor-related protein 5 ...
Dec 11, 2007 · Our study aimed to evaluate the importance of LRP5 ... Conclusion: Common variations of the LRP5 promoter are associated with BMD in young women.
[13]
Wnt/β-catenin signalling: function, biological mechanisms ... - Nature
Jan 3, 2022 · When Wnts are recognized by FZD and LRP5/6, the “destruction complex” is recruited to the cell membrane by interacting with FZD, which loses the ...
[14]
Paternal sleep deprivation induces metabolic perturbations in male ...
Feb 20, 2023 · ... DNA methylation in the promoter of Lrp5 ... Furthermore, lots of factors can influence DNA methylation, includes histone modification, noncoding ...
[15]
Paternal sleep deprivation induces metabolic perturbations in male ...
Mechanistically, in pancreatic islets of SD-F1 offspring, we identified alterations in DNA methylation at the promoter region of the LRP5 (LDL receptor related ...
[16]
microRNA-23a inhibits osteogenic differentiation of human bone ...
Our data indicate that miR-23a plays an inhibitory role in osteogenic differentiation of hBMSCs, which may act by targeting LRP5. Keywords: Human bone marrow- ...
[17]
miR-375-3p negatively regulates osteogenesis by targeting and ...
In conclusion, we revealed miR-375-3p negatively regulated osteogenesis by targeting LRP5 and β-catenin. ... miRNA Target Expression Vector (Promega) digested ...
[18]
miR-29 Modulates Wnt Signaling in Human Osteoblasts through a ...
Mature miRNAs modulate gene expression by base pairing to complementary sequences within an mRNA target. Through their association with the RNA-induced ...
[19]
Mutations in LRP5 or FZD4 Underlie the Common Familial ...
LRP5 consists of 23 exons and encodes a 1,615–amino acid protein. Its extracellular segment contains four domains, each composed of six YWTD repeats (which form ...
[20]
Lrp5 and Lrp6 in Development and Disease - PMC - PubMed Central
Low-density lipoprotein-related receptors 5 and 6 (LRP5/6) are highly homologous proteins with key functions in canonical Wnt signaling.
[21]
Characterization of the Interaction of Sclerostin with the Low Density ...
LRP5 and LRP6 are proteins predicted to contain four six-bladed β-propeller domains and both bind the bone-specific Wnt signaling antagonist sclerostin.
[22]
Structure of the Wnt–Frizzled–LRP6 initiation complex reveals the ...
The structure of the signaling-competent Wnt–Frizzled–LRP6 complex reveals the basis for initiating canonical Wnt/β-catenin signaling.Missing: LRP arrowhead-
[23]
LRP5 - Low-density lipoprotein receptor-related protein 5 - UniProt
Apr 12, 2005 · Acts as a coreceptor with members of the frizzled family of seven-transmembrane spanning receptors to transduce signal by Wnt proteins.
[24]
603506 - LOW DENSITY LIPOPROTEIN RECEPTOR-RELATED ...
(2001) determined that the LRP5 gene contains 23 coding exons and spans more than 100 kb. Twells et al. (2001) determined that the LRP5 gene spans 160 kb. ▻ ...
[25]
Identification of targets of the Wnt pathway destruction complex in ...
Mar 31, 2009 · ... (Lrp5/6) receptors facilitates the phosphorylation of Lrp5/6 cytoplasmic tail by GSK3 (4). This triggers the interaction of the Frizzled–Lrp5 ...
[26]
The function of endocytosis in Wnt signaling
Sep 14, 2017 · Overexpression of these ligases causes downregulation of Frizzled receptors and Lrp5/6 at the cell surface by targeting the receptors for ...
[27]
LRP5 and LRP6 in Wnt Signaling: Similarity and Divergence
The extracellular domain of LRP5 and LRP6 contains four tandem YWTD-type β-propeller (BP) domains, each followed by an epidermal growth factor (EGF)-like domain ...
[28]
Page not found | Nature
**Summary:**
[29]
An LDL-receptor-related protein mediates Wnt signalling in mice
Here we present evidence that a new member of the low-density lipoprotein (LDL)-receptor-related protein family, LRP6 (ref. 3), is critical for Wnt signalling ...Missing: co- paper
[30]
https://www.molbiolcell.org/doi/10.1091/mbc.e08-07-0711
[31]
The Extracellular Domain of Lrp5/6 Inhibits Noncanonical Wnt ...
Dec 3, 2008 · Lrp5/6 are crucial coreceptors for Wnt/β-catenin signaling, a pathway biochemically distinct from noncanonical Wnt signaling pathways.
[32]
LDL Receptor-Related Protein 5 (LRP5) Affects Bone Accrual and ...
We report that LRP5, encoding the low-density lipoprotein receptor-related protein 5, affects bone mass accrual during growth.
[33]
Wnt co-receptors Lrp5 and Lrp6 differentially mediate Wnt3a ...
Canonical Wnt signaling has been shown to promote osteoblast differentiation, enhance osteoblast proliferation, maturation and mineralization, and inhibit ...
[34]
Attenuation of WNT signaling by DKK-1 and -2 regulates BMP2 ...
Oct 30, 2007 · ... RANKL and OPG expression, resulting in a negative signal for osteoclast formation. Osteoclastogenesis is further dampened by Wnt3a's ability ...
[35]
BMP-2 Modulates β-Catenin Signaling Through Stimulation of Lrp5 ...
We found that BMP-2 stimulates Lrp5 expression and inhibits the expression of β-TrCP, the F-box E3 ligase responsible for β-catenin degradation.Missing: integration fracture healing
[36]
Wnt Pathway in Bone Repair and Regeneration - Frontiers
Jan 6, 2019 · Bone regeneration for fracture repair and defect healing ... Integration of BMP, Wnt, and notch signaling pathways in osteoblast differentiation.
[37]
Role of Wnt signaling in fracture healing - PMC - PubMed Central
Generally, activation of Wnt signaling is helpful to accelerate bone repair, and mutations in β-catenin or LRP5/6 reduce bone healing. Moreover, inhibition of ...Missing: integration | Show results with:integration
[38]
LRP5/6 directly bind to Frizzled and prevent Frizzled-regulated ...
Apr 22, 2015 · Here we report that Wnt receptor Frizzled (Frz) and theco-receptors LRP5 and LRP6 (LRP5/6) directly interact with each other and this interaction is regulated ...
[39]
LDL receptor-related proteins 5 and 6 in Wnt/beta-catenin signaling
We discuss Arrow/Lrp5/Lrp6 interactions with Wnt and the Frizzled family of Wnt receptors, and with the intracellular beta-catenin degradation apparatus. We ...<|control11|><|separator|>
[40]
Frizzled and LRP5/6 receptors for Wnt/β-catenin signaling - PubMed
Dec 1, 2012 · Frizzled and LRP5/6 are Wnt receptors that, when activated, lead to the stabilization of cytoplasmic β-catenin.Missing: ternary paper<|separator|>
[41]
Low-density lipoprotein receptor-related protein-5 binds to Axin and ...
We identified Axin as a protein that interacts with the intracellular domain of LRP-5. LRP-5, when expressed in fibroblast cells, showed no effect on the ...
[42]
Interaction between LRP5 and Frat1 mediates the activation of the ...
We demonstrate here that LRP5/Frat1 interaction is involved in beta-catenin nuclear translocation and TCF-1 transcriptional activation.
[43]
Wnt5a promotes Frizzled-4 signalosome assembly by ... - PubMed
May 1, 2017 · These results complement our understanding of lipoprotein receptor-related proteins 5 and 6 (LRP5/6), Dishevelled, and Axin signalosome assembly ...
[44]
Surrogate Wnt agonists that phenocopy canonical ... - PubMed - NIH
May 11, 2017 · Here we develop surrogate Wnt agonists, water-soluble FZD-LRP5/LRP6 heterodimerizers, with FZD5/FZD8-specific and broadly FZD-reactive binding domains.<|separator|>
[45]
LRP5 and LRP6 in development and disease - PubMed - NIH
Here, we discuss the links between alterations in LRP5/6 and disease, proteins that interact with them, and insights gained into their function from mouse ...
[46]
https://www.jbc.org/article/S0021-9258(20)87312-8/fulltext
[47]
https://www.jbc.org/content/287/20/16454.long
[48]
Distinct roles of LRP5 and LRP6 in Wnt signaling regulation in the ...
The roles of Wnt co-receptors LRP5 and LRP6 in Wnt signaling regulation remain elusive, as most retinal cells express both of the co-receptors. To address this ...
[49]
Sclerostin inhibits Wnt signaling through tandem interaction with two ...
Oct 23, 2020 · SOST inhibits new bone formation and growth by binding to LRP5/6, thereby inhibiting canonical Wnt signaling in osteoblasts. Sclerosteosis, ...
[50]
Structure of the Wnt–Frizzled–LRP6 initiation complex reveals the ...
The structure of the signaling-competent Wnt–Frizzled–LRP6 complex reveals the basis for initiating canonical Wnt/β-catenin signaling.
[51]
https://www.pnas.org/doi/10.1073/pnas.2218238120
[52]
Osteoporosis-pseudoglioma syndrome - Orphanet
Diagnostic methods. Diagnosis is suspected on clinical presentation (typically congenital blindness and white pupils) and confirmed by genetic testing.Missing: criteria | Show results with:criteria
[53]
Structure and Function of the Retina of Low-density Lipoprotein ...
Loss-of-function mutations in the Wnt co-receptor, low-density lipoprotein receptor-related protein 5 (LRP5), result in familial exudative vitreoretinopathy ...
[54]
High Bone Density Due to a Mutation in LDL-Receptor–Related ...
Genetic analysis revealed linkage of the syndrome to chromosome 11q12–13 (odds of linkage, >1 million to 1), an interval that contains LRP5. Affected members of ...<|separator|>
[55]
Entry - #601884 - BONE MINERAL DENSITY QUANTITATIVE TRAIT ...
A number sign (#) is used with this entry because bone mineral density variation (BMND1) can result from mutation in the LRP5 gene (603506) on chromosome ...Missing: gain- function
[56]
144750 - ENDOSTEAL HYPEROSTOSIS, AUTOSOMAL DOMINANT
Autosomal dominant endosteal hyperostosis is a generalized bone dysplasia characterized by a cortical thickening of the long bones, with no alteration in ...
[57]
Relationship of LRP5rs121908669(G171R) genotypes to femur T ...
Feb 8, 2023 · LRP5G171R(LRP5rs121908669) is a proven pathogenic single nucleotide polymorphism SNP for a disease associated with high bone mass HBM. There ...
[58]
A Case of Endosteal Hyperostosis Caused by a Mutation of the Low ...
May 30, 2025 · A rare disease caused by a gain-of-function mutation of the low-density lipoprotein receptor-related protein 5 (LRP5) gene leading to endosteal hyperostosis.<|control11|><|separator|>
[59]
Reduced Affinity to and Inhibition by DKK1 Form a Common ...
Wnt1, Wnt10b, and Wnt3a were able to activate canonical signaling in 293T cells that had not been transfected with LRP5 (Fig. 4A to D). This activation may be ...Missing: values | Show results with:values
[60]
High Bone Mass–Causing Mutant LRP5 Receptors Are Resistant to ...
This second mechanism implies that resistance to SOST and DKK1 is due to less LRP5 reaching the cell surface, rather than to reduced affinity between LRP5 ...
[61]
Six Novel Missense Mutations in the LDL Receptor-Related Protein ...
The LDL receptor-related protein 5 (LRP5) gene has been shown to be involved in both osteoporosis-pseudoglioma syndrome and the high–bone-mass phenotype and ...
[62]
LRP5 high bone mass (Worth-type autosomal dominant endosteal ...
Sep 2, 2023 · LRP5 high bone mass (HBM) is an autosomal dominant endosteal hyperostosis caused by mutations of the low-density lipoprotein receptor-related protein 5 (LRP5) ...Missing: 601884 | Show results with:601884