Calcium and activity-dependent signaling in the developing cerebral cortex

被引:15
|
作者
McKinney, Arpana Arjun [1 ,2 ,3 ,4 ]
Petrova, Ralitsa [2 ,3 ,4 ,5 ]
Panagiotakos, Georgia [1 ,2 ,3 ,4 ]
机构
[1] Univ Calif San Francisco, Grad Program Dev & Stem Cell Biol, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Eli & Edythe Broad Ctr Regenerat Med & Stem Cell R, San Francisco, CA 94143 USA
[3] Univ Calif San Francisco, Dept Biochem & Biophys, San Francisco, CA 94143 USA
[4] Univ Calif San Francisco, Kavli Inst Neurosci, San Francisco, CA 94143 USA
[5] Teva Pharmaceut, Redwood City, CA 94063 USA
来源
DEVELOPMENT | 2022年 / 149卷 / 17期
基金
美国国家卫生研究院;
关键词
Calcium signaling; Cortical development; Neurodevelopmental disorders; OLIGODENDROCYTE PRECURSOR CELLS; CORTICAL INTERNEURON MIGRATION; NFAT1 TRANSCRIPTION FACTOR; PERMEABLE AMPA RECEPTORS; CENTRAL-NERVOUS-SYSTEM; GENE-EXPRESSION; NEURONAL MIGRATION; NMDA RECEPTORS; PROGENITOR CELLS; RADIAL MIGRATION;
D O I
10.1242/dev.198853
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Calcium influx can be stimulated by various intra-and extracellular signals to set coordinated gene expression programs into motion. As such, the precise regulation of intracellular calcium represents a nexus between environmental cues and intrinsic genetic programs. Mounting genetic evidence points to a role for the deregulation of intracellular calcium signaling in neuropsychiatric disorders of developmental origin. These findings have prompted renewed enthusiasm for understanding the roles of calcium during normal and dysfunctional prenatal development. In this Review, we describe the fundamental mechanisms through which calcium is spatiotemporally regulated and directs early neurodevelopmental events. We also discuss unanswered questions about intracellular calcium regulation during the emergence of neurodevelopmental disease, and provide evidence that disruption of cell-specific calcium homeostasis and/or redeployment of developmental calcium signaling mechanisms may contribute to adult neurological disorders. We propose that understanding the normal developmental events that build the nervous system will rely on gaining insights into cell type-specific calcium signaling mechanisms. Such an understanding will enable therapeutic strategies targeting calcium -dependent mechanisms to mitigate disease.
引用
收藏
页数:21
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