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少突胶质前体细胞:中枢神经系统中不断进行有丝分裂的细胞。

Oligodendrocyte progenitor cells: the ever mitotic cells of the CNS.

作者信息

Neumann Bjoern, Kazanis Ilias

机构信息

Wellcome Trust- MRC Cambridge Stem Cell Institute, Allbutt Building, Cambridge Biomedical Campus, Hill Road, Cambridge, CB2 0AH, UK,

出版信息

Front Biosci (Schol Ed). 2016 Jan 1;8(1):29-43. doi: 10.2741/s444.

Abstract

Oligodendrocyte Progenitor Cells (OPCs) first appear at mid embryogenic stages during development of the mammalian CNS and a mitotically active population of them remains present even into late adulthood. During the life-time of the organism they initially proliferate and migrate in order to populate the whole nervous tissue, then they massively generate oligodendrocytesand finally they switch to a less mitotically active phase generating new oligodendrocytes at a slow rate in the adult brain; importantly, they can regenerate acutely or chronically destroyed myelin. All the above depend on the capacity of OPCs to regulate their cell cycle within different contexts. In this review we describe the development of OPCs, their differential mitotic behavior in various conditions (embryo, disease, ageing), we discuss what is known about the mechanisms that control their cell cycle and wehighlightfew interesting and still open questions.

摘要

少突胶质前体细胞(OPCs)最早出现在哺乳动物中枢神经系统发育的胚胎中期阶段,并且即使到成年后期,仍有一群具有有丝分裂活性的少突胶质前体细胞存在。在生物体的生命周期中,它们最初进行增殖和迁移,以便遍布整个神经组织,然后大量生成少突胶质细胞,最后进入有丝分裂活性较低的阶段,在成人大脑中以缓慢的速度生成新的少突胶质细胞;重要的是,它们能够急性或慢性再生被破坏的髓鞘。上述所有情况都依赖于少突胶质前体细胞在不同环境中调节其细胞周期的能力。在这篇综述中,我们描述了少突胶质前体细胞的发育过程、它们在各种条件下(胚胎、疾病、衰老)的不同有丝分裂行为,我们讨论了已知的控制其细胞周期的机制,并强调了一些有趣且仍未解决的问题。

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