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肠神经胶质细胞

Enteric glia.

作者信息

Gershon M D, Rothman T P

机构信息

Department of Anatomy and Cell Biology, Columbia University College of Physicians and Surgeons, New York, New York 10032.

出版信息

Glia. 1991;4(2):195-204. doi: 10.1002/glia.440040211.

Abstract

The structure of the enteric nervous system (ENS) is different from that of extraenteric peripheral nerve. Collagen is excluded from the enteric plexuses and support for neuronal elements is provided by astrocyte-like enteric glial cells. Enteric glia differ from Schwann cells in that they do not form basal laminae and they ensheath axons, not individually, but in groups. Although enteric glia are rich in the S-100 and glial fibrillary acidic proteins, it has been difficult to find a single chemical marker that distinguishes enteric glia from non-myelinating Schwann cells. Nevertheless, two monoclonal antibodies have been obtained that recognize antigens that are expressed on Schwann cells (Ran-1 in rats and SMP in avians) but not enteric glia. Functional differences between enteric glia and non-myelinating Schwann cells, including responses to gliotoxins and in vitro proliferative rates, have also been observed. Developmentally, enteric glia, like Schwann cells, are derived from the neural crest. In both mammals and birds the precursors of the ENS appear to migrate to the bowel from sacral as well as vagal levels of the crest. These crest-derived emigrés give rise to both enteric glia and neurons; however, analyses of the ontogeny of the enteric innervation in a mutant mouse (the ls/ls), in which the original colonizing waves of crest-derived precursor cells are unable to invade the terminal colon, suggest that enteric glia can also arise from Schwann cells that enter the gut with the extrinsic innervation. When induced to leave back-transplanted segments of avian bowel, enteric crest-derived cells migrate into peripheral nerves and form Schwann cells. Enteric glia and Schwann cells thus appear to be different cell types, but ones that derive from lineages that diverge relatively late in ontogeny.

摘要

肠神经系统(ENS)的结构与肠外周围神经不同。肠丛中没有胶原蛋白,星形胶质细胞样的肠神经胶质细胞为神经元成分提供支持。肠神经胶质细胞与施万细胞不同,它们不形成基膜,它们包裹轴突,不是单个包裹,而是成组包裹。尽管肠神经胶质细胞富含S-100和胶质纤维酸性蛋白,但很难找到一种单一的化学标记物来区分肠神经胶质细胞和无髓施万细胞。然而,已经获得了两种单克隆抗体,它们识别在施万细胞(大鼠中的Ran-1和禽类中的SMP)上表达但不在肠神经胶质细胞上表达的抗原。还观察到了肠神经胶质细胞和无髓施万细胞之间的功能差异,包括对神经胶质毒素的反应和体外增殖率。在发育过程中,肠神经胶质细胞与施万细胞一样,都源自神经嵴。在哺乳动物和鸟类中,ENS的前体似乎从神经嵴的骶部以及迷走神经水平迁移到肠道。这些源自神经嵴的移民产生了肠神经胶质细胞和神经元;然而,对一种突变小鼠(ls/ls)的肠内神经支配个体发生的分析表明,肠神经胶质细胞也可以由随着外在神经支配进入肠道的施万细胞产生,在这种突变小鼠中,源自神经嵴的前体细胞的原始定植波无法侵入终末结肠。当诱导离开禽类肠道的回植段时,源自肠神经嵴的细胞迁移到外周神经并形成施万细胞。因此,肠神经胶质细胞和施万细胞似乎是不同的细胞类型,但它们源自个体发生中相对较晚分化的谱系。

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