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Synaptic pruning

Synaptic pruning is a critical developmental process in the mammalian brain whereby excess synapses—connections between neurons—are selectively eliminated to refine neural circuits and enhance their efficiency.^[1] This targeted removal of functional synapses, often involving the dismantling of presynaptic terminals and postsynaptic elements, occurs primarily during early postnatal life and adolescence, reducing synaptic density from peak levels (up to 50% higher than in adults) to more streamlined adult configurations.^[2] Driven by neural activity, the process follows principles of competition where active synapses are strengthened and stabilized, while inactive or weak ones are tagged for elimination, ensuring precise wiring for sensory processing, learning, and behavior.^[2] The biological mechanisms underlying synaptic pruning integrate neural activity with immune and cellular signaling pathways. In the developing visual system, for instance, spontaneous retinal waves before eye opening initiate pruning in the retinogeniculate circuit to segregate inputs from each eye, while post-eye-opening visual experience further refines connections through activity-dependent competition.^[2] Key players include microglia, the brain's resident immune cells, which engulf and remove tagged synapses via processes like trogocytosis, guided by complement proteins (e.g., C1q and C3) and fractalkine signaling.^[1] Major histocompatibility complex class I (MHC-I) molecules also contribute by restricting synapse density and enabling activity-dependent elimination.^[2] This activity reliance aligns with Hebbian principles—"cells that fire together wire together"—whereby correlated activity promotes synapse maintenance, and decorrelated or deprived activity triggers pruning, as seen in monocular deprivation experiments that shift ocular dominance in the visual cortex.^[2] Synaptic pruning's importance lies in its role in optimizing brain architecture for efficient information processing and adaptability. By eliminating redundant connections, it enhances signal-to-noise ratios in neural networks, supporting cognitive functions like memory consolidation and sensory acuity.^[1] Disruptions in this process are implicated in neurodevelopmental disorders: excessive pruning has been linked to schizophrenia, potentially contributing to reduced synaptic density in prefrontal regions, while insufficient pruning may underlie autism spectrum disorders, leading to hyperconnectivity.^[1] Recent studies from 2023-2025 provide direct evidence of impaired synaptic pruning in autism via compromised immune cell function, update the synaptic hypothesis of schizophrenia emphasizing multi-hit vulnerability, and identify synaptic pruning gene networks correlated with Alzheimer's neuropathology and cognitive decline.^[3]^[4]^[5] In neurodegenerative contexts, such as Alzheimer's disease, aberrant pruning mechanisms involving microglia and complement could exacerbate synapse loss.^[1] Ongoing research explores therapeutic modulation of these pathways, highlighting pruning's dual role in both healthy development and pathology.

Overview

Definition

Synaptic pruning is the selective elimination of excess or weak synapses during neural development, a process that refines neural circuits by removing unnecessary connections and strengthening those that are functionally relevant, thereby enhancing the efficiency and specificity of brain wiring.^[6] This targeted removal occurs primarily through the phagocytosis of synaptic elements by glial cells, but the core outcome is the streamlining of connectivity to support mature cognitive and behavioral functions.^[7] In early brain development, synapses are overproduced in a phase known as synaptogenesis, generating up to 50% more connections than required for adult circuitry, particularly in regions like the human frontal cortex where synaptic density peaks around 1-2 years of age.^[8] Pruning then counters this overproduction by eliminating redundant or less active synapses, transitioning the brain from a diffuse, exploratory network to a more optimized, specialized one. This process is distinct from synaptogenesis, which involves the formation of new synapses, and from synaptic plasticity mechanisms like long-term potentiation or depression, which adjust the strength of existing synapses without their physical removal.^[7] The timeline of synaptic pruning features prominent peaks during infancy, when initial refinements occur rapidly postnatally, and again during adolescence, with a sharp decline in synaptic density leading to adult-like stabilization.^[6] This elimination is driven by activity-dependent competition, where synapses involved in correlated neural activity are preferentially preserved, while inactive or mismatched ones are tagged for removal, ensuring circuits adapt to experiential demands.^[9]

Historical Background

The concept of synaptic pruning emerged from early postmortem studies of human brain tissue in the 1970s, when neurologist Peter Huttenlocher quantified synapse density in the frontal cortex across age groups. Using electron microscopy on samples from infants to adults, Huttenlocher observed that synaptic density peaks around age 1–2 years, reaching approximately 1.66 × 10^9 synapses per cubic millimeter (50% above adult levels of ~1.1 × 10^9 synapses/mm³), before declining by about 33% to adult levels by adolescence, indicating a natural elimination process during development.^[10] This work provided the first direct evidence of synapse overproduction followed by selective reduction in humans, challenging prior assumptions of static neural connectivity.^[8] In the 1980s and 1990s, research shifted toward understanding the activity-dependent nature of pruning, particularly in the visual system of animal models. Carla Shatz and her collaborators demonstrated through experiments in fetal and postnatal cats that spontaneous neural activity drives the refinement of retinogeniculate connections, where initially diffuse axonal projections segregate into precise eye-specific layers via competitive elimination of weak synapses. Extending these findings to ferrets, whose visual system develops postnatally similar to humans, Shatz's team showed that disrupting correlated activity with tetrodotoxin blocks this pruning, resulting in persistent overlapping connections and underscoring the role of patterned firing in circuit maturation. These studies established synaptic pruning as a dynamic, experience-guided process essential for functional wiring. The molecular mechanisms underlying pruning gained clarity in the 2000s with the identification of immune components as key mediators. Beth Stevens and colleagues discovered that complement proteins C1q and C3 tag synapses for elimination in the developing retinogeniculate system of mice, localizing to a subset of synapses during the peak pruning period around postnatal day 5–10.^[9] Deficiency in C1q or C3 led to sustained excess synapses, confirming their necessity for microglia-mediated phagocytosis without affecting synapse formation. This breakthrough linked innate immunity to neural development, revealing pruning as an active tagging-and-clearance process. Advances in the 2020s have enabled real-time visualization of pruning dynamics using two-photon microscopy for in vivo imaging. Techniques combining genetic labeling of synapses with high-resolution two-photon excitation have captured microglia engulfing tagged dendritic spines in the mouse olfactory bulb over hours, revealing rapid, activity-modulated elimination dynamics during critical windows.^[11] These observations, previously limited to static snapshots, highlight the spatiotemporal precision of pruning and its responsiveness to sensory input.

Developmental Role

Early Brain Development

Synaptic pruning initiates during the prenatal period, beginning in utero as neural circuits form and refine through activity-dependent mechanisms driven by spontaneous neural activity. In the retinogeniculate pathway, retinal ganglion cell axons initially project diffusely to the dorsal lateral geniculate nucleus (dLGN), where excess connections are eliminated to establish eye-specific segregation; this process is evident in animal models such as cats and mice, where prenatal retinal waves guide early refinement of thalamocortical projections. Similarly, thalamocortical connections undergo initial pruning in utero, sculpting foundational wiring between thalamic nuclei and cortical targets before birth.^[12]^[2] Following birth, synaptic pruning undergoes a postnatal surge, particularly in sensory cortices, where rapid elimination of superfluous synapses refines neural circuits for processing environmental inputs. In humans, this is prominent in the visual and auditory cortices from birth to approximately 2-3 years of age, coinciding with heightened synaptogenesis and subsequent overproduction of connections that must be pared down for efficiency. For instance, in the visual cortex, synapse density increases dramatically in the first few months postpartum, supporting the maturation of retinogeniculate inputs to primary visual areas. This surge ensures the consolidation of essential pathways while discarding inactive ones, laying the groundwork for sensory perception.^[1]^[13] Quantitative assessments reveal that synapse density in human sensory cortices peaks between approximately 4 and 12 months postpartum, reaching levels up to 150% of adult values in the visual cortex, before declining progressively through pruning. By age 10, this density has dropped by approximately 40-50%, approaching adult-like configurations as circuits stabilize. These changes are most pronounced in early sensory regions, where overproduction facilitates adaptability but requires selective elimination to optimize signal transmission.^[14] Pruning in early development is highly dependent on sensory input, with deprivation leading to aberrant refinement of neural circuits. In cases of congenital cataracts, which block patterned visual experience from birth until surgical correction, the visual cortex exhibits disrupted pruning, resulting in persistent increases in cortical thickness and imbalances in excitatory-inhibitory signaling even after sight restoration. This underscores the role of experience in directing the elimination of unused synapses, preventing maladaptive overconnectivity in sensory areas.^[15]^[16]

Adolescent Refinement

Synaptic pruning reaches its peak during adolescence in the human prefrontal cortex and association areas, primarily between ages 12 and 20, where excitatory synapse density decreases by up to 40%.^[17] This process refines neural circuits in higher-order regions responsible for complex cognition, contrasting with earlier developmental phases focused on sensory areas.^[18] The reduction in synaptic density is evidenced by postmortem studies showing prolonged spine density in layer III pyramidal neurons of the dorsolateral prefrontal cortex until around age 16, followed by a sharp decline.^[18] This adolescent pruning correlates strongly with the maturation of executive functions, such as decision-making and impulse control, by enhancing the signal-to-noise ratio in prefrontal circuits. By eliminating weaker or unused connections, pruning streamlines information processing, reducing neural "white noise" and improving the efficiency of task-relevant signaling, which supports behavioral adaptations during this period.^[19] Disruptions in this refinement can create vulnerability windows for cognitive and emotional dysregulation, highlighting adolescence as a sensitive period for circuit optimization.^[20] Sex differences in adolescent synaptic pruning are notable, with the process occurring slightly earlier in females, often aligned with the onset of puberty around ages 10-12 compared to 12-14 in males.^[21] This temporal shift is influenced by pubertal hormones, particularly estrogen, which modulates synaptic plasticity and promotes earlier refinement in female prefrontal and hippocampal regions.^[22] In rodents, similar patterns emerge, with females exhibiting more pronounced pruning of dendritic spines during adolescence than males.^[23] Cross-species comparisons reveal conserved patterns of adolescent synaptic pruning in rodents and non-human primates, underscoring its role as a critical period for circuit stabilization across mammals.^[21] In rats and mice, prefrontal synapse elimination peaks during the equivalent of human adolescence (postnatal days 28-60), mirroring human timelines and contributing to stabilized executive-like behaviors.^[23] Primate studies, including macaques, show analogous reductions in prefrontal synaptic density during juvenile-to-adolescent transitions, reinforcing the evolutionary preservation of this mechanism for cognitive maturation.^[24]

Mechanisms

Axonal Processes

During synaptic pruning, axons undergo degeneration through a Wallerian-like process that targets distal segments following the tagging of weak synapses for elimination. This breakdown initiates locally at the presynaptic terminal and propagates distally, dismantling axonal branches without affecting the neuronal cell body.^[25] The process involves the activation of caspase enzymes, particularly caspase-3 and caspase-6, which cleave cytoskeletal proteins such as actin and tubulin, leading to fragmentation and disassembly of the axonal structure.^[26] Caspase activity in this context is distinct from apoptotic pathways, as it selectively drives axon degeneration while preserving neuronal viability.^[25] In contrast to full degeneration, axon retraction represents an active withdrawal of presynaptic terminals without complete axonal breakdown, allowing for rapid refinement of connections. This mechanism is prominent in the developing neuromuscular junction, where excess axonal branches retract toward the soma in response to competitive interactions among motor neurons.^[27] Retraction involves the dynamic reorganization of the presynaptic membrane and cytoskeleton, often triggered by reduced trophic support or activity-dependent signals, resulting in the selective elimination of polyinnervated synapses.^[28] Axon shedding occurs through the mechanical release of axonal fragments, facilitated by interactions with surrounding cells that exert physical forces to detach segments. This process has been observed in the developing neuromuscular junction, where glial cells contribute to fragmenting and displacing axonal pieces during circuit refinement.^[29] Electron microscopy studies provide direct evidence of these axonal changes, revealing fragmented axons and retracted terminals in pruned regions during critical developmental periods. Serial section electron microscopy of neuromuscular junctions, for instance, shows distal axonal segments undergoing piecemeal disassembly, with accumulated debris in refining arbors.^[30]

Glial and Immune Involvement

Synaptic pruning involves the activation of the classical complement cascade, where the protein C1q binds to weak or inactive synapses, initiating downstream signaling that leads to the deposition of C3 for opsonization and subsequent recruitment of phagocytic cells.^[31] This process was first demonstrated in the developing retinogeniculate system, where C1q localizes to synapses during peak pruning periods, and its absence results in disrupted synapse elimination.^[31] The complement components C1q and C3 tag synapses for removal, marking them as targets for engulfment by microglia, thereby facilitating the refinement of neural circuits.^[32] Microglia serve as the primary phagocytes in synaptic pruning, actively engulfing tagged synapses through receptors such as P2Y12 and TREM2. The P2Y12 receptor enables microglial process extension toward synaptic sites, supporting the detection and removal of unnecessary connections during visual cortex plasticity.^[33] Similarly, TREM2 signaling is crucial for microglial-mediated synaptic refinement in early brain development, as its deficiency impairs the phagocytosis of excess synapses and alters circuit maturation.^[34] These receptors allow microglia to respond to complement-opsonized synapses, ensuring selective elimination without widespread neuronal damage.^[32] Astrocytes contribute to pruning by modulating synapse stability through secreted factors like thrombospondins and hevin, which influence the formation and maintenance of excitatory synapses. Thrombospondins, released by astrocytes, promote synaptogenesis by bridging neurexins and neuroligins on pre- and postsynaptic elements, but their regulated expression helps balance synapse addition and removal during development.^[28] In contrast, hevin acts to refine connectivity by disrupting certain neurexin-neuroligin interactions, thereby promoting the elimination of inappropriate spines and stabilizing functional circuits at dendritic sites.^[35] These astrocytic proteins thus fine-tune the pruning process, complementing immune-mediated mechanisms. The pruning process exhibits activity dependence, with high-activity synapses evading complement tagging and phagocytosis, while low-activity ones are preferentially marked and removed to optimize circuit efficiency. Recent studies (as of 2025) highlight neuron-to-glia and glia-to-glia signaling pathways directing experience-dependent glial synapse pruning.^[36]^[37] This selectivity is evident in models like C1qa knockout mice, where the lack of C1q leads to excessive retention of multi-innervated synapses in the retinogeniculate pathway, demonstrating dysregulation and impaired refinement.^[31] Such findings underscore the immune-glial axis's role in experience-driven circuit sculpting.

Functions and Variations

Circuit Optimization

Synaptic pruning plays a crucial role in refining neural circuits by selectively eliminating redundant synaptic connections, thereby reducing the metabolic and material costs associated with maintaining an overabundant network. This process minimizes wiring volume and energy expenditure in the brain, as excessive connections would otherwise impose significant physiological burdens on neural tissue. By removing these superfluous synapses, pruning prevents potential circuit overload, allowing for more streamlined signal transmission without interference from unused pathways.^[38] Pruning also enhances the specificity of neural circuits by strengthening frequently used pathways while weakening or eliminating those that are infrequently activated, aligning with the Hebbian principle encapsulated in the "use it or lose it" maxim. Under this activity-dependent framework, synapses involved in correlated firing patterns are stabilized and reinforced, promoting efficient information routing and functional specialization within networks. This refinement ensures that neural circuits become more precise, focusing resources on pathways essential for adaptive behavior and sensory processing.^[39]^[40] Quantitatively, the adult human brain contains approximately $1.5 \times 10^{14} synapses, a substantial reduction from the peak overproduction during early childhood, where synaptic density can exceed adult levels by 50-100% depending on the region. This downsizing optimizes circuit performance, including faster signal propagation due to decreased synaptic clutter and improved temporal precision in neural responses. Such scaling underscores pruning's role in balancing developmental exuberance with mature efficiency. A prominent example of circuit optimization through pruning is observed in the refinement of ocular dominance columns in the visual cortex, where monocular deprivation experiments demonstrate activity-dependent elimination of synapses from the deprived eye. In these studies, closing one eye during a critical developmental window leads to a selective loss of synaptic connections favoring the open eye, thereby sharpening columnar organization and enhancing visual processing specificity.^[41]^[18]

Experience-Dependent Adaptations

Synaptic pruning exhibits distinct modes of regulation, with a form of genetically programmed elimination occurring in non-sensory brain areas largely independent of sensory input. In regions such as the cerebellum, multiple climbing fiber inputs to Purkinje cells are refined to a single dominant connection through intrinsic molecular signaling, including metabotropic glutamate receptor 1 (mGluR1)-mediated release of semaphorin 7A and brain-derived neurotrophic factor, which drive synapse withdrawal without reliance on external activity.^[7] This activity-independent process ensures foundational circuit sculpting in areas not directly tied to immediate environmental cues, contrasting with sensory-driven refinements elsewhere.^[7] Experience-dependent adaptations in synaptic pruning are prominently observed in sensory systems, where environmental inputs selectively stabilize or eliminate connections based on usage. For instance, in the developing visual cortex, normal visual experience promotes the elimination of weak or unused retinogeniculate synapses during a critical period, refining connectivity to match functional demands; conversely, sensory deprivation through dark-rearing delays this pruning, leading to retention of excess synapses and prolonged juvenile circuit states.^[42] Similar patterns emerge in auditory and somatosensory cortices, where patterned sensory activity, often mediated briefly by microglial engulfment of less active terminals, drives the selective removal of underutilized connections to enhance circuit specificity.^[7] Beyond circuit refinement, synaptic pruning plays a key role in learning by facilitating the forgetting of outdated or irrelevant connections, thereby preventing interference and supporting efficient information processing. This process, akin to homeostatic scaling-down during sleep, weakens low-utility synapses through mechanisms involving Arc and Homer1a proteins, which reduce synaptic strength proportionally to prior activity levels and improve signal-to-noise ratios for retained memories.^[43] However, excessive pruning can disrupt memory consolidation by prematurely eliminating synapses involved in engram stabilization, potentially hindering the integration of new learning with existing knowledge.^[43] Synaptic pruning also links to broader physiological demands, conserving metabolic resources in the energy-intensive brain, which accounts for approximately 20% of the body's total energy expenditure despite comprising only 2% of body mass. By reducing the number of synapses—often by up to 50% in certain cortical regions during development—this elimination optimizes neural efficiency, minimizing ATP costs associated with maintaining inactive connections. These adaptations intensify during puberty, with discontinuous waves of pruning in prefrontal and association areas coinciding with reproductive maturation, potentially reallocating metabolic resources from exuberant early connectivity toward energy demands for sexual development and adult behavioral flexibility.^[44]

Pathological Aspects

Neurodevelopmental Disorders

Aberrant synaptic pruning has been implicated in the pathophysiology of autism spectrum disorder (ASD), where deficits in the pruning process during early development lead to an excess of synaptic connections, particularly in cortical regions involved in social cognition. Postmortem analyses of brain tissue from children with ASD reveal approximately 50% higher synaptic density compared to neurotypical individuals by late childhood, attributed to impaired elimination of unnecessary synapses mediated by overactive mTOR signaling and reduced macroautophagy in microglia.^[45] This excessive connectivity disrupts the excitatory-inhibitory balance in social brain networks, such as the prefrontal cortex and amygdala, contributing to core symptoms like impaired social interaction and sensory processing atypicalities. Furthermore, induced pluripotent stem cell-derived astrocytes from individuals with ASD exhibit significantly reduced expression of complement component 4 (C4), a key mediator of microglial synaptic engulfment, which further impairs pruning efficiency and fosters atypical neural circuit refinement.^[46] In attention-deficit/hyperactivity disorder (ADHD), synaptic pruning is notably delayed, particularly in prefrontal cortical areas responsible for executive functions, resulting in prolonged retention of immature neural connections that correlate with attention and impulse control deficits. Longitudinal MRI studies demonstrate that peak cortical thickness in children with ADHD occurs about three years later than in typically developing peers, with the most pronounced delays in the dorsolateral prefrontal cortex, reflecting a lag in gray matter thinning associated with synaptic elimination. This maturational delay extends into adolescence, where inefficient pruning in frontostriatal circuits hinders the refinement of cognitive control networks, exacerbating hyperactivity and inattention symptoms.^[47]^[48] Neuroimaging evidence supports these pruning abnormalities across ASD and ADHD. Positron emission tomography (PET) using the synaptic vesicle protein 2A ligand ^11^C-UCB-J reveals approximately 17% lower synaptic density throughout the cortex in adults with ASD, particularly in the prefrontal regions, suggesting that early pruning deficits may lead to compensatory over-pruning or degeneration later in life, which aligns with social impairment severity. In ADHD, structural MRI consistently shows regionally specific delays in cortical thinning as a proxy for reduced pruning, while PET imaging indicates altered dopamine-related synaptic activity in prefrontal areas, underscoring connectivity disruptions tied to attention deficits.^[49]^[47] Animal models provide mechanistic insights into these disorders through maternal immune activation (MIA) paradigms, where pregnant mice exposed to viral mimetics like poly(I:C) produce offspring with pruning deficits mimicking ASD features. In these models, male offspring display increased dendritic spine density in the hippocampus due to impaired microglial function, evidenced by reduced CX3CR1 expression, leading to behavioral anomalies such as social deficits and perseverative behaviors without gross neuropathology.^[50] Similar MIA-induced alterations in synaptic pruning have been observed in rat models relevant to ADHD-like hyperactivity, highlighting immune-mediated disruptions in circuit optimization during critical developmental windows.^[51] While aberrant pruning patterns in schizophrenia involve excessive synapse elimination in prefrontal regions, contributing to cognitive decline, the mechanisms in ASD and ADHD emphasize under-pruning or delays that preserve immature circuits.^[52]

Potential Therapeutic Targets

One promising avenue for therapeutic intervention in disorders involving aberrant synaptic pruning targets the complement system, which tags synapses for microglial phagocytosis. Inhibitors of complement components such as C1q and C3 have shown potential in preclinical models to reduce excessive pruning associated with schizophrenia. For instance, genetic ablation or pharmacological blockade of C1q and C3 in mouse models prevents over-pruning in the prefrontal cortex, preserving synaptic density and improving behavioral outcomes in schizophrenia-like phenotypes.^[53]^[54] Recent studies in the 2020s have advanced this approach, with small-molecule inhibitors of C3 demonstrating reduced microglial engulfment of synapses in rodent models of neurodevelopmental risk, suggesting a pathway for clinical translation.^[55] Microglial modulators, particularly colony-stimulating factor 1 receptor (CSF1R) inhibitors, offer another targeted strategy to regulate phagocytosis rates during pruning. In autism spectrum disorder (ASD) mouse models, such as those with maternal immune activation, CSF1R inhibitors like PLX3397 transiently deplete microglia, normalizing excessive synaptic elimination and correcting synaptic dysfunction without long-term neuronal loss.^[56] These agents restore balanced circuit refinement, as evidenced by improved social behaviors and synaptic protein expression in treated animals.^[57] Preclinical data from 2020 onward indicate that timed CSF1R inhibition during critical developmental windows enhances therapeutic efficacy, highlighting its role in modulating glial-neuronal interactions.^[58] Repurposed antibiotics like minocycline have emerged as accessible modulators of microglial activity, dampening overactive pruning in adolescent mental health contexts. By inhibiting microglial activation and synaptic engulfment, minocycline ameliorates behavioral deficits in depression and schizophrenia models, with reduced phagocytic microglia observed in treated rodents.^[59] Clinical trials, including phase II studies such as the BeneMin trial (completed in 2018), demonstrate its promise in early psychosis intervention, where it attenuates inflammation-linked pruning abnormalities and supports adolescent brain maturation.^[60] Meta-analyses confirm modest but significant improvements in negative symptoms, underscoring minocycline's potential as an adjunct therapy.^[61] Advancements in imaging technologies, such as super-resolution microscopy, are facilitating real-time monitoring of pruning dynamics in vivo, paving the way for personalized therapeutic strategies. Techniques like stimulated emission depletion (STED) microscopy enable nanoscale visualization of synaptic elimination in living mouse brains, tracking microglial-synapse interactions during development.^[62] Integrated with two-photon imaging, these methods reveal pruning deficits in disease models, guiding targeted interventions like complement blockade.^[11] By 2025, such imaging has informed preclinical trial designs, allowing assessment of therapeutic impacts on synaptic stability.^[63]

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Aug 7, 2025 · Moreover, our results indicated that minocycline treatment dampened microglial activation, decreased the phagocytic microglia density, reduced ...
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Synaptic Pruning in Schizophrenia: Does Minocycline Modulate ...
Recent studies suggest that the tetracycline antibiotic minocycline, or its cousins, hold therapeutic potential for affective and psychotic disorders.Missing: trials activity phase 2025
[53]
Microglia Activation and Schizophrenia: Lessons From the Effects of ...
Jun 27, 2016 · Minocycline significantly alters microglia-mediated engulfment and synaptic pruning in the retinogeniculate system at early postnatal stages.30 ...Missing: II | Show results with:II
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Synaptic pruning mechanisms and application of emerging imaging
Synaptic pruning is a crucial process in synaptic refinement, eliminating unstable synaptic connections in neural circuits. This process is triggered and ...
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In vivo super-resolution of the brain – How to visualize the hidden ...
Aug 17, 2022 · Applications of super-resolution in the anesthetized mouse brain enlighten the stability and plasticity of synaptic nanostructures. These ...Missing: pruning | Show results with:pruning