小胶质细胞
神经科学
生物
特雷姆2
神经可塑性
突触发生
神经发生
CX3CR1型
轴突引导
受体
轴突
趋化因子
趋化因子受体
免疫学
炎症
遗传学
作者
Subrata Pramanik,Hyde Thomas M,Saswata Chakrabarty,Berkay Paylar,Ajay Pradhan,Manisha Thaker,Shamini Ayyadhury,Arulmani Manavalan,Per‐Erik Olsson,Gopal Pramanik,Klaus Heese
标识
DOI:10.1016/j.neubiorev.2024.105834
摘要
Microglia, the intrinsic neuroimmune cells residing in the central nervous system (CNS), exert a pivotal influence on brain development, homeostasis, and functionality, encompassing critical roles during both aging and pathological states. Recent advancements in comprehending brain plasticity and functions have spotlighted conspicuous variances between male and female brains, notably in neurogenesis, neuronal myelination, axon fasciculation, and synaptogenesis. Nevertheless, the precise impact of microglia on sex-specific brain cell plasticity, sculpting diverse neural network architectures and circuits, remains largely unexplored. This article seeks to unravel the present understanding of microglial involvement in brain development, plasticity, and function, with a specific emphasis on microglial signaling in brain sex polymorphism. Commencing with an overview of microglia in the CNS and their associated signaling cascades, we subsequently probe recent revelations regarding molecular signaling by microglia in sex-dependent brain developmental plasticity, functions, and diseases. Notably, C-X3-C motif chemokine receptor 1 (CX3CR1), triggering receptors expressed on myeloid cells 2 (TREM2), calcium (Ca
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