神经发生
异丙酚
生物
神经干细胞
小RNA
基因沉默
神经科学
双皮质醇
干细胞
药理学
细胞生物学
海马体
基因
遗传学
齿状回
作者
Qiliang Jiang,Yingwei Wang,Xueyin Shi
出处
期刊:Stem Cells and Development
[Mary Ann Liebert]
日期:2016-10-31
卷期号:26 (3): 189-196
被引量:34
标识
DOI:10.1089/scd.2016.0257
摘要
Prolonged or high-dose exposure to anesthetics, such as propofol, can cause brain cell degeneration and subsequent long-term learning or memory deficits, particularly in the developing brain. However, the cellular and molecular mechanisms underlying the deleterious effects of propofol at certain stages of development remain unclear. In this study we found that propofol inhibited the proliferation, neuronal differentiation, and migration of neural stem cells (NSCs) while upregulating miR-141-3p. Silencing of miR-141-3p abrogated the effects of propofol on NSC neurogenesis. Propofol treatment downregulated IGF2BP2, a direct target of miR-141-3p, whereas overexpression of IGF2BP2 attenuated the effects of propofol and miR-141-3p on NSC neurogenesis. In short, propofol inhibits NSC neurogenesis through a mechanism involving the miR-141-3p/IGF2BP2 axis. Our results may provide a potential approach for preventing the neurodegenerative effects of propofol in the developing brain.
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