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Notch受体激活会抑制少突胶质细胞的分化。

Notch receptor activation inhibits oligodendrocyte differentiation.

作者信息

Wang S, Sdrulla A D, diSibio G, Bush G, Nofziger D, Hicks C, Weinmaster G, Barres B A

机构信息

Stanford University School of Medicine, Department of Neurobiology, California 94305, USA.

出版信息

Neuron. 1998 Jul;21(1):63-75. doi: 10.1016/s0896-6273(00)80515-2.

Abstract

In this study, we show that oligodendrocyte differentiation is powerfully inhibited by activation of the Notch pathway. Oligodendrocytes and their precursors in the developing rat optic nerve express Notch1 receptors and, at the same time, retinal ganglion cells express Jagged1, a ligand of the Notch1 receptor, along their axons. Jagged1 expression is developmentally regulated, decreasing with a time course that parallels myelination in the optic nerve. These results suggest that the timing of oligodendrocyte differentiation and myelination is controlled by the Notch pathway and raise the question of whether localization of myelination is controlled by this pathway.

摘要

在本研究中,我们发现Notch信号通路的激活会强烈抑制少突胶质细胞的分化。发育中的大鼠视神经中的少突胶质细胞及其前体细胞表达Notch1受体,同时,视网膜神经节细胞沿其轴突表达Notch1受体的配体Jagged1。Jagged1的表达受发育调控,其表达随时间下降,这一过程与视神经髓鞘形成的时间进程平行。这些结果表明,少突胶质细胞分化和髓鞘形成的时间由Notch信号通路控制,并提出了髓鞘形成的定位是否受该信号通路控制的问题。

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