生物
重编程
神经元
视网膜
谱系(遗传)
基因敲除
多嘧啶结合蛋白
电池类型
皮质激素生成
神经科学
神经胶质
穆勒胶质细胞
细胞
星形胶质细胞
细胞生物学
基因
干细胞
遗传学
基因亚型
中枢神经系统
选择性拼接
祖细胞
作者
Thanh D. Hoang,Dong-Won Kim,Haley Appel,Nicole A. Pannullo,Patrick J. Leavey,Manabu Ozawa,Sika Zheng,Minzhong Yu,Neal S. Peachey,Ju-Hyun Kim,Seth Blackshaw
标识
DOI:10.1101/2021.10.04.462784
摘要
Abstract Direct reprogramming of glia into neurons is a potentially promising approach for the replacement of neurons lost to injury or neurodegenerative disorders. Knockdown of the polypyrimidine tract-binding protein Ptbp1 has been recently reported to induce efficient conversion of retinal Müller glia and brain astrocytes into functional neurons. However, genetic analysis of Ptbp1 function in adult glia has not been conducted. Here, we use a combination of genetic lineage tracing, scRNA-Seq, and electrophysiological analysis to show that specific deletion of Ptbp1 in adult retinal Müller glia and brain astrocytes does not lead to any detectable level of glia-to-neuron conversion. Only a few changes in gene expression are observed in glia following Ptbp1 deletion, and glial identity is maintained. These findings highlight the importance of using genetic manipulation and lineage tracing methods in studying cell type conversion.
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