突触发生
星形胶质细胞
细胞生物学
下调和上调
线粒体生物发生
生物
代谢型谷氨酸受体5
谷氨酸受体
生物发生
线粒体
神经科学
神经胶质
代谢型谷氨酸受体
受体
中枢神经系统
生物化学
基因
作者
Tamara Zehnder,Francesco Petrelli,Jennifer Romanos,Eva C de Oliveira Figueiredo,Tommy L. Lewis,Nicole Déglon,Franck Polleux,Mirko Santello,Paola Bezzi
出处
期刊:Cell Reports
[Cell Press]
日期:2021-04-01
卷期号:35 (2): 108952-108952
被引量:114
标识
DOI:10.1016/j.celrep.2021.108952
摘要
The mechanisms controlling the post-natal maturation of astrocytes play a crucial role in ensuring correct synaptogenesis. We show that mitochondrial biogenesis in developing astrocytes is necessary for coordinating post-natal astrocyte maturation and synaptogenesis. The astrocytic mitochondrial biogenesis depends on the transient upregulation of metabolic regulator peroxisome proliferator-activated receptor gamma (PPARγ) co-activator 1α (PGC-1α), which is controlled by metabotropic glutamate receptor 5 (mGluR5). At tissue level, the loss or downregulation of astrocytic PGC-1α sustains astrocyte proliferation, dampens astrocyte morphogenesis, and impairs the formation and function of neighboring synapses, whereas its genetic re-expression is sufficient to restore the mitochondria compartment and correct astroglial and synaptic defects. Our findings show that the developmental enhancement of mitochondrial biogenesis in astrocytes is a critical mechanism controlling astrocyte maturation and supporting synaptogenesis, thus suggesting that astrocytic mitochondria may be a therapeutic target in the case of neurodevelopmental and psychiatric disorders characterized by impaired synaptogenesis.
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