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Sexual dimorphism of complement-dependent microglial synaptic pruning and other immune pathways in the developing brain

https://doi.org/10.1101/204412

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1001/jamapsychiatry.2013.272openalex-snapshot

Microglial Activation in Young Adults With Autism Spectrum Disorder

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Neuroglial activation and neuroinflammation in the brain of patients with autism

inferredcites →https://doi.org/10.1002/glia.23176openalex-snapshot

Generation of a microglial developmental index in mice and in humans reveals a sex difference in maturation and immune reactivity

inferredcites →https://doi.org/10.1007/s11481-011-9299-yopenalex-snapshot

A Lifespan Approach to Neuroinflammatory and Cognitive Disorders: A Critical Role for Glia

inferredcites →https://doi.org/10.1016/j.bbi.2007.10.003openalex-snapshot

Early-life infection leads to altered BDNF and IL-1β mRNA expression in rat hippocampus following learning in adulthood

inferredcites →https://doi.org/10.1016/j.bbr.2005.12.002openalex-snapshot

A behavioural characterization of neonatal infection-facilitated memory impairment in adult rats

inferredcites →https://doi.org/10.1016/j.biopsych.2010.05.024openalex-snapshot

Microglial Activation and Increased Microglial Density Observed in the Dorsolateral Prefrontal Cortex in Autism

inferredcites →https://doi.org/10.1016/j.cell.2007.10.036openalex-snapshot

The Classical Complement Cascade Mediates CNS Synapse Elimination

inferredcites →https://doi.org/10.1016/j.cell.2016.04.001openalex-snapshot

Progranulin Deficiency Promotes Circuit-Specific Synaptic Pruning by Microglia via Complement Activation

inferredcites →https://doi.org/10.1016/j.conb.2013.09.012openalex-snapshot

Phagocytic glial cells: sculpting synaptic circuits in the developing nervous system

inferredcites →https://doi.org/10.1016/j.conb.2015.12.004openalex-snapshot

New insights on the role of microglia in synaptic pruning in health and disease

inferredcites →https://doi.org/10.1016/j.devcel.2016.07.006openalex-snapshot

Microglia: Phagocytosing to Clear, Sculpt, and Eliminate

inferredcites →https://doi.org/10.1016/j.it.2015.08.008openalex-snapshot

Microglia: Dynamic Mediators of Synapse Development and Plasticity

inferredcites →https://doi.org/10.1016/j.jsbmb.2015.09.039openalex-snapshot

Sex differences in neurodevelopmental and neurodegenerative disorders: Focus on microglial function and neuroinflammation during development

inferredcites →https://doi.org/10.1016/j.nbd.2008.01.012openalex-snapshot

Immune transcriptome alterations in the temporal cortex of subjects with autism

inferredcites →https://doi.org/10.1016/j.neuron.2012.03.026openalex-snapshot

Microglia Sculpt Postnatal Neural Circuits in an Activity and Complement-Dependent Manner

inferredcites →https://doi.org/10.1016/j.yhbeh.2012.02.018openalex-snapshot

Sex, glia, and development: Interactions in health and disease

inferredcites →https://doi.org/10.1016/s0074-7742(05)71013-8openalex-snapshot

Immunological Findings in Autism

inferredcites →https://doi.org/10.1037/0735-7044.119.1.293openalex-snapshot

Neonatal Infection Induces Memory Impairments Following an Immune Challenge in Adulthood.

inferredcites →https://doi.org/10.1038/nature10110openalex-snapshot

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

inferredcites →https://doi.org/10.1038/nature10523openalex-snapshot

Spatio-temporal transcriptome of the human brain

inferredcites →https://doi.org/10.1038/nature20612openalex-snapshot

Genome-wide changes in lncRNA, splicing, and regional gene expression patterns in autism

inferredcites →https://doi.org/10.1038/ncomms10717openalex-snapshot

Gene expression in human brain implicates sexually dimorphic pathways in autism spectrum disorders

inferredcites →https://doi.org/10.1038/ncomms6748openalex-snapshot

Transcriptome analysis reveals dysregulation of innate immune response genes and neuronal activity-dependent genes in autism

inferredcites →https://doi.org/10.1038/nn.3641openalex-snapshot

Deficient neuron-microglia signaling results in impaired functional brain connectivity and social behavior

inferredcites →https://doi.org/10.1038/nrn3978openalex-snapshot

Immune mediators in the brain and peripheral tissues in autism spectrum disorder

inferredcites →https://doi.org/10.1038/srep21181openalex-snapshot

Sex Biased Gene Expression Profiling of Human Brains at Major Developmental Stages

inferredcites →https://doi.org/10.1038/tp.2011.62openalex-snapshot

Identification of autoimmune gene signatures in autism

inferredcites →https://doi.org/10.1042/bst0380476openalex-snapshot

Synapse elimination during development and disease: immune molecules take centre stage

inferredcites →https://doi.org/10.1111/j.1471-4159.2011.07630.xopenalex-snapshot

Sex differences in microglial colonization of the developing rat brain

inferredcites →https://doi.org/10.1126/science.aad8373openalex-snapshot

Complement and microglia mediate early synapse loss in Alzheimer mouse models

inferredcites →https://doi.org/10.1155/2016/2827090openalex-snapshot

Sex and Gender Differences in Central Nervous System-Related Disorders

inferredcites →https://doi.org/10.1186/s13229-015-0061-9openalex-snapshot

Gene expression analysis in Fmr1KO mice identifies an immunological signature in brain tissue and mGluR5-related signaling in primary neuronal cultures

inferredcites →https://doi.org/10.1189/jlb.1205707openalex-snapshot

The immune response in autism: a new frontier for autism research

inferredcites →https://doi.org/10.1523/jneurosci.3688-11.2011openalex-snapshot

Microglia and Memory: Modulation by Early-Life Infection

inferredcites →https://doi.org/10.3389/fnins.2014.00235openalex-snapshot

New roles for Fc receptors in neurodegeneration-the impact on Immunotherapy for Alzheimer's Disease

inferredcites →https://doi.org/10.4049/jimmunol.0903833openalex-snapshot

Systemic Inflammation Modulates Fc Receptor Expression on Microglia during Chronic Neurodegeneration

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.1002/dev.22473openalex-snapshot

Synaptic pruning during adolescence shapes adult social behavior in both males and females

inferred← citeshttps://doi.org/10.1007/s00281-018-0726-5openalex-snapshot

Sex differences in vaccine-induced humoral immunity

inferred← citeshttps://doi.org/10.1038/s41467-018-06118-zopenalex-snapshot

Microglial dopamine receptor elimination defines sex-specific nucleus accumbens development and social behavior in adolescent rats

inferred← citeshttps://doi.org/10.1101/2022.11.06.515311openalex-snapshot

Integrative single-cell characterization of hypothalamus sex-differential and obesity-associated genes and regulatory elements

inferred← citeshttps://doi.org/10.1101/211029openalex-snapshot

Microglial elimination of dopamine D1 receptors defines sex-specific changes in nucleus accumbens development and social play behavior during adolescence

inferred← citeshttps://doi.org/10.1126/scitranslmed.abe9726openalex-snapshot

In utero exposure to maternal anti–aquaporin-4 antibodies alters brain vasculature and neural dynamics in male mouse offspring

inferred← citeshttps://doi.org/10.3390/ijms20092270openalex-snapshot

Sex-Dependent Effects of Perinatal Inflammation on the Brain: Implication for Neuro-Psychiatric Disorders

inferred← citeshttps://doi.org/10.3410/f.734066247.793551885openalex-snapshot

Faculty Opinions recommendation of Microglial dopamine receptor elimination defines sex-specific nucleus accumbens development and social behavior in adolescent rats.

inferred← citeshttps://doi.org/10.3410/f.734066247.793553635openalex-snapshot

Faculty Opinions recommendation of Microglial dopamine receptor elimination defines sex-specific nucleus accumbens development and social behavior in adolescent rats.

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