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神经系统中细胞因子介导的细胞命运调控的潜在机制。

Mechanisms underlying cytokine-mediated cell-fate regulation in the nervous system.

作者信息

Nakashima Kinichi, Taga Tetsuya

机构信息

Department of Cell Fate Modulation, Institute of Molecular Embryology and Genetics, Kumamoto University, Japan.

出版信息

Mol Neurobiol. 2002 Jun;25(3):233-44. doi: 10.1385/MN:25:3:233.

Abstract

Neurons, astrocytes, and oligodendrocytes, the three major cell types in the nervous system, are generated from common neural stem cells during development. Recent studies have provided evidence that neural stem cells are preserved in the adult brain, where, until recently, neurogenesis had not been considered to take place. The mechanisms that gOvern the fate of neural stem-cell determination have yet to be clarified. It is becoming apparent that soluble protein mediators referred to as cytokines play critical roles in cell-fate determination. For instance, bone morphogenetic proteins (BMPs) alter the fate of developing brain cells from a neurogenic differentiation to an astrocytic one. Different types of cytokines sometimes cooperate to modulate differentiation. For example, the interleukin-6 (IL-6) family cytokines and the BMP family cytokines act in synergy to elaborate astrocyte differentiation. In this review, we focus on recent progress that addresses the molecular mechanisms whereby cytokines regulate the fate of cells in neural lineages. We also discuss possible clinical applications of these findings to minimize the undesirable gliogenesis that occurs after neural stem-cell implantation and nerve injury.

摘要

神经元、星形胶质细胞和少突胶质细胞是神经系统中的三种主要细胞类型,在发育过程中由共同的神经干细胞产生。最近的研究表明,神经干细胞在成人大脑中得以保留,而直到最近,人们一直认为成人大脑中不会发生神经发生。决定神经干细胞命运的机制尚待阐明。越来越明显的是,被称为细胞因子的可溶性蛋白质介质在细胞命运决定中起着关键作用。例如,骨形态发生蛋白(BMPs)会将发育中的脑细胞命运从神经源性分化转变为星形细胞分化。不同类型的细胞因子有时会协同调节分化。例如,白细胞介素-6(IL-6)家族细胞因子和BMP家族细胞因子协同作用以促进星形胶质细胞分化。在本综述中,我们重点关注近期在解决细胞因子调节神经谱系中细胞命运的分子机制方面取得的进展。我们还将讨论这些发现可能的临床应用,以尽量减少神经干细胞植入和神经损伤后发生的不良胶质细胞生成。

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