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
[Elsevier]
日期:2021-04-01
卷期号:35 (2): 108952-108952
被引量:43
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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