Microglia roles in synaptic plasticity and myelination in homeostatic conditions and neurodevelopmental disorders

被引:80
作者
Bar, Ela [1 ,2 ,3 ]
Barak, Boaz [1 ,2 ]
机构
[1] Tel Aviv Univ, Sch Psychol Sci, Fac Social Sci, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Sagol Sch Neurosci, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Fac Life Sci, Sch Neurobiol Biochem & Biophys, Tel Aviv, Israel
关键词
autism; microglia; myelin; neurodevelopmental disorders; synaptic plasticity; CENTRAL-NERVOUS-SYSTEM; DORSOLATERAL PREFRONTAL CORTEX; OLIGODENDROCYTE LINEAGE CELLS; TOLL-LIKE RECEPTORS; BRAIN-DEVELOPMENT; MOUSE MODEL; VAL66MET POLYMORPHISM; MULTIPLE-SCLEROSIS; CLEARANCE FUNCTION; DOWN-REGULATION;
D O I
10.1002/glia.23637
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Microglia are the immune cells of the brain, involved in synapse formation, circuit sculpting, myelination, plasticity, and cognition. Being active players during early development as well as in adulthood, microglia affect other cells directly by their long processes and unique receptors and indirectly by secreting growth factors and cytokines. In this review, we discuss the roles of microglia in neurodevelopmental disorders, synaptic plasticity, myelination, and homeostatic conditions throughout human and mouse development. Within these processes, we specifically focus on the contribution of altered microglial interactions with neurons and oligodendrocytes, altered cytokine and growth factor activities, and alterations in the complement system. We conclude by highlighting future perspectives and providing an overview of future research on microglia.
引用
收藏
页码:2125 / 2141
页数:17
相关论文
共 221 条
[1]   Gastrointestinal flora and gastrointestinal status in children with autism-comparisons to typical children and correlation with autism severity [J].
Adams, James B. ;
Johansen, Leah J. ;
Powell, Linda D. ;
Quig, David ;
Rubin, Robert A. .
BMC GASTROENTEROLOGY, 2011, 11
[2]   Microglia Enhance Synapse Activity to Promote Local Network Synchronization [J].
Akiyoshi, Ryohei ;
Wake, Hiroaki ;
Kato, Daisuke ;
Horiuchi, Hiroshi ;
Ono, Riho ;
Ikegami, Ako ;
Haruwaka, Koichiro ;
Omori, Toshiaki ;
Tachibana, Yoshihisa ;
Moorhouse, Andrew J. ;
Nabekura, Junichi .
ENEURO, 2018, 5 (05)
[3]   Immune function of microglia [J].
Aloisi, F .
GLIA, 2001, 36 (02) :165-179
[4]   Shank3mutation in a mouse model of autism leads to changes in the S-nitroso-proteome and affects key proteins involved in vesicle release and synaptic function [J].
Amal, Haitham ;
Barak, Boaz ;
Bhat, Vadiraja ;
Gong, Guanyu ;
Joughin, Brian A. ;
Wang, Xin ;
Wishnok, John S. ;
Feng, Guoping ;
Tannenbaum, Steven R. .
MOLECULAR PSYCHIATRY, 2020, 25 (08) :1835-1848
[5]   Altered white matter connectivity as a neural substrate for social impairment in Autism Spectrum Disorder [J].
Ameis, Stephanie H. ;
Catani, Marco .
CORTEX, 2015, 62 :158-181
[6]   Attention-Deficit/Hyperactivity Disorder And Inflammation: What Does Current Knowledge Tell Us? A Systematic Review [J].
Anand, Deepa ;
Colpo, Gabriela D. ;
Zeni, Gregory ;
Zeni, Cristian P. ;
Teixeira, Antonio L. .
FRONTIERS IN PSYCHIATRY, 2017, 8
[7]   Fractalkine Signaling and Microglia Functions in the Developing Brain [J].
Arnoux, Isabelle ;
Audinat, Etienne .
NEURAL PLASTICITY, 2015, 2015
[8]   Transcriptional profiling reveals evidence for signaling and oligodendroglial abnormalities in the temporal cortex from patients with major depressive disorder [J].
Aston, C ;
Jiang, L ;
Sokolov, BP .
MOLECULAR PSYCHIATRY, 2005, 10 (03) :309-322
[9]   Neuronal deletion of Gtf2i, associated with Williams syndrome, causes behavioral and myelin alterations rescuable by a remyelinating drug [J].
Barak, Boaz ;
Zhang, Zicong ;
Liu, Yuanyuan ;
Nir, Ariel ;
Trangle, Sari S. ;
Ennis, Michaela ;
Levandowski, Kirsten M. ;
Wang, Dongqing ;
Quast, Kathleen ;
Boulting, Gabriella L. ;
Li, Yi ;
Bayarsaihan, Dashzeveg ;
He, Zhigang ;
Feng, Guoping .
NATURE NEUROSCIENCE, 2019, 22 (05) :700-+
[10]   Neurobiology of social behavior abnormalities in autism and Williams syndrome [J].
Barak, Boaz ;
Feng, Guoping .
NATURE NEUROSCIENCE, 2016, 19 (05) :647-655