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少突胶质细胞祖细胞发育迁移的机制。

Mechanisms of oligodendrocyte progenitor developmental migration.

作者信息

Xia Wenlong, Fancy Stephen P J

机构信息

Department of Neurology, University of California, San Francisco, San Francisco, California, USA.

Department of Pediatrics, University of California, San Francisco, San Francisco, California, USA.

出版信息

Dev Neurobiol. 2021 Nov;81(8):985-996. doi: 10.1002/dneu.22856. Epub 2021 Oct 24.

Abstract

Oligodendrocytes, the myelinating cells of the central nervous system (CNS), develop from oligodendrocyte progenitor cells (OPCs) that must first migrate extensively throughout the developing brain and spinal cord. Specified at particular times from discrete regions in the developing CNS, OPCs are one of the most migratory of cell types and disperse rapidly. A variety of factors act on OPCs to trigger intracellular changes that regulate their migration. We will discuss factors that act as long-range guidance cues, those that act to regulate cellular motility, and those that are critical in determining the final positioning of OPCs. In addition, recent evidence has identified the vasculature as the physical substrate used by OPCs for their migration. Several new findings relating to this oligodendroglial-vascular signaling axis reveal new insight on the relationship between OPCs and blood vessels in the developing and adult brain.

摘要

少突胶质细胞是中枢神经系统(CNS)的髓鞘形成细胞,由少突胶质前体细胞(OPC)发育而来,而OPC必须首先在发育中的脑和脊髓中广泛迁移。OPC在发育中的中枢神经系统的特定时间从离散区域分化而来,是迁移能力最强的细胞类型之一,并且迅速分散。多种因素作用于OPC,触发调节其迁移的细胞内变化。我们将讨论作为远程引导信号的因素、调节细胞运动的因素以及对确定OPC的最终定位至关重要的因素。此外,最近的证据表明,脉管系统是OPC迁移所利用的物理基质。与这种少突胶质细胞-血管信号轴相关的几项新发现揭示了发育中和成体脑中OPC与血管之间关系的新见解。

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