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神经胶质生成:历史视角,1839年至1985年

Gliogenesis: historical perspectives, 1839-1985.

作者信息

Webster Henry deF, Aström Karl E

机构信息

Neuroimmunology Branch, National Institute of Neurological Diseases and Stroke MSC, Bethesda, MD 20892-1400, USA.

出版信息

Adv Anat Embryol Cell Biol. 2009;202:1-109.

Abstract

This historical review of gliogenesis begins with Schwann's introduction of the cell doctrine in 1839. Subsequent microscopic studies revealed the cellular structure of many organs and tissues, but the CNS was thought to be different. In 1864, Virchow created the concept that nerve cells are held together by a "Nervenkitte" which he called"glia" (for glue). He and his contemporaries thought that "glia" was an unstructured, connective tissue-like ground substance that separated nerve cells from each other and from blood vessels. Dieters, a pupil of Virchow, discovered that this ground substance contained cells, which he described and illustrated. Improvements in microscopes and discovery of metallic impregnation methods finally showed convincingly that the "glia" was not a binding substance. Instead, it was composed of cells, each separate and distinct from neighboring cells and each with its own characteristic array of processes. Light microscopic studies of developing and mature nervous tissue led to the discovery of different types of glial cells-astroglia, oligodendroglia, microglia, and ependymal cells in the CNS, and Schwann cells in the peripheral nervous system (PNS). Subsequent studies characterized the origins and development of each type of glial cell. A new era began with the introduction of electron microscopy, immunostaining, and in vitro maintenance of both central and peripheral nervous tissue. Other methods and models greatly expanded our understanding of how glia multiply, migrate, and differentiate. In 1985, almost a century and a half of study had produced substantial progress in our understanding of glial cells, including their origins and development. Major advances were associated with the discovery of new methods. These are summarized first. Then the origins and development of astroglia, oligodendroglia, microglia, ependymal cells, and Schwann cells are described and discussed. In general, morphology is emphasized. Findings related to cytodifferentiation, cellular interactions, functions, and regulation of developing glia have also been included.

摘要

对神经胶质生成的这一历史回顾始于1839年施旺提出的细胞学说。随后的显微镜研究揭示了许多器官和组织的细胞结构,但人们认为中枢神经系统有所不同。1864年,魏尔啸提出神经细胞由一种他称为“神经组织”(意为“胶水”)的物质维系在一起的概念。他和他的同时代人认为“神经组织”是一种无结构的、类似结缔组织的基质,将神经细胞彼此分隔,并将它们与血管分隔开来。魏尔啸的学生迪特斯发现这种基质包含细胞,并对其进行了描述和绘图。显微镜的改进以及金属浸染方法的发现最终令人信服地表明,“神经组织”并非一种结合物质。相反,它由细胞组成,每个细胞都与相邻细胞分开且不同,并且每个细胞都有其独特的突起排列。对发育中和成熟神经组织的光学显微镜研究导致发现了不同类型的神经胶质细胞——中枢神经系统中的星形胶质细胞、少突胶质细胞、小胶质细胞和室管膜细胞,以及周围神经系统中的施万细胞。随后的研究对每种类型神经胶质细胞的起源和发育进行了表征。随着电子显微镜、免疫染色以及中枢和周围神经组织的体外培养技术的引入,一个新时代开始了。其他方法和模型极大地扩展了我们对神经胶质细胞如何增殖、迁移和分化的理解。1985年,经过近一个半世纪的研究,我们对神经胶质细胞的理解,包括它们的起源和发育,取得了重大进展。主要进展与新方法的发现有关。首先对这些进行总结。然后描述并讨论星形胶质细胞、少突胶质细胞、小胶质细胞、室管膜细胞和施万细胞的起源和发育。总体而言,重点是形态学。还包括了与细胞分化、细胞间相互作用、功能以及发育中神经胶质细胞的调节相关的研究结果。

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