微泡
神经干细胞
神经发生
生物
赫斯1
细胞生物学
小RNA
外体
干细胞
基因沉默
胚胎干细胞
星形胶质细胞
神经球
细胞分化
神经科学
成体干细胞
信号转导
中枢神经系统
遗传学
基因
Notch信号通路
作者
Ping Yuan,Lu Ding,Huili Chen,Yi Wang,Chunhong Li,Shuang Zhao,Xiaoyu Yang,Yizhao Ma,Jie Zhu,Xin-Rui Qi,Yanyan Zhang,Xiaohuan Xia,Jialin Zheng
标识
DOI:10.3389/fcell.2021.601600
摘要
Exosomes, a key element of the central nervous system microenvironment, mediate intercellular communication via horizontally transferring bioactive molecules. Emerging evidence has implicated exosomes in the regulation of neurogenesis. Recently, we compared the neurogenic potential of exosomes released from primary mouse embryonic neural stem cells (NSCs) and astrocyte-reprogrammed NSCs, and observed diverse neurogenic potential of those two exosome populations in vitro . However, the roles of NSC-derived exosomes on NSC differentiation and the underlying mechanisms remain largely unknown. In this study, we firstly demonstrated that NSC-derived exosomes facilitate the differentiation of NSCs and the maturation of both neuronal and glial cells in defined conditions. We then identified miR-9, a pro-neural miRNA, as the most abundantly expressed miRNA in NSC-derived exosomes. The silencing of miR-9 in exosomes abrogates the positive effects of NSC-derived exosomes on the differentiation of NSCs. We further identified Hes1 as miR-9 downstream target, as the transfection of Hes1 siRNA restored the differentiation promoting potential of NSC-derived exosomes after knocking down exosomal miR-9. Thus, our data indicate that NSC-derived exosomes facilitate the differentiation of NSCs via transferring miR-9, which sheds light on the development of cell-free therapeutic strategies for treating neurodegeneration.
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