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小鼠星形胶质细胞中 Notch 信号调控的潜在神经发生程序。

A latent neurogenic program in astrocytes regulated by Notch signaling in the mouse.

机构信息

Department of Cell and Molecular Biology, Karolinska Institute, SE-171 77 Stockholm, Sweden.

Lund Stem Cell Center, University Hospital, SE-221 84 Lund, Sweden.

出版信息

Science. 2014 Oct 10;346(6206):237-41. doi: 10.1126/science.346.6206.237. Epub 2014 Oct 9.

Abstract

Neurogenesis is restricted in the adult mammalian brain; most neurons are neither exchanged during normal life nor replaced in pathological situations. We report that stroke elicits a latent neurogenic program in striatal astrocytes in mice. Notch1 signaling is reduced in astrocytes after stroke, and attenuated Notch1 signaling is necessary for neurogenesis by striatal astrocytes. Blocking Notch signaling triggers astrocytes in the striatum and the medial cortex to enter a neurogenic program, even in the absence of stroke, resulting in 850 ± 210 (mean ± SEM) new neurons in a mouse striatum. Thus, under Notch signaling regulation, astrocytes in the adult mouse brain parenchyma carry a latent neurogenic program that may potentially be useful for neuronal replacement strategies.

摘要

神经发生在成年哺乳动物的大脑中受到限制;在正常生活中,大多数神经元既不被交换,也不在病理情况下被替换。我们报告说,中风会引发小鼠纹状体星形胶质细胞中的潜在神经发生程序。中风后星形胶质细胞中的 Notch1 信号减少,减弱的 Notch1 信号对于纹状体星形胶质细胞的神经发生是必要的。阻断 Notch 信号会触发纹状体和内侧皮质中的星形胶质细胞进入神经发生程序,即使在没有中风的情况下也是如此,导致一只老鼠的纹状体中产生 850 ± 210(平均值 ± SEM)个新神经元。因此,在 Notch 信号调节下,成年小鼠脑实质中的星形胶质细胞携带潜在的神经发生程序,这可能对神经元替代策略有用。

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