祖细胞
神经发生
星形胶质细胞
神经干细胞
细胞生物学
神经科学
生物
内皮干细胞
神经细胞
神经球
干细胞
细胞
成体干细胞
中枢神经系统
生物化学
遗传学
体外
作者
Wenlu Li,Emiri T. Mandeville,Violeta Durán‐Laforet,Norito Fukuda,Zhanyang Yu,Yi Zheng,Aaron Held,Jihyun Park,Takafumi Nakano,Masayoshi Tanaka,Jingfei Shi,Elga Esposito,Wanting Niu,Changhong Xing,Kazuhide Hayakawa,Ignacio Lizasoaín,Klaus van Leyen,Xunming Ji,Brian J. Wainger,Marı́a A. Moro,Eng H. Lo
标识
DOI:10.1038/s41467-022-35498-6
摘要
The concept of the neurovascular unit emphasizes the importance of cell-cell signaling between neural, glial, and vascular compartments. In neurogenesis, for example, brain endothelial cells play a key role by supplying trophic support to neural progenitors. Here, we describe a surprising phenomenon where brain endothelial cells may release trans-differentiation signals that convert astrocytes into neural progenitor cells in male mice after stroke. After oxygen-glucose deprivation, brain endothelial cells release microvesicles containing pro-neural factor Ascl1 that enter into astrocytes to induce their trans-differentiation into neural progenitors. In mouse models of focal cerebral ischemia, Ascl1 is upregulated in endothelium prior to astrocytic conversion into neural progenitor cells. Injecting brain endothelial-derived microvesicles amplifies the process of astrocyte trans-differentiation. Endothelial-specific overexpression of Ascl1 increases the local conversion of astrocytes into neural progenitors and improves behavioral recovery. Our findings describe an unexpected vascular-regulated mechanism of neuroplasticity that may open up therapeutic opportunities for improving outcomes after stroke.
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