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关于胃肠道中Cajal间质细胞作为起搏器和神经传递介质的案例。

A case for interstitial cells of Cajal as pacemakers and mediators of neurotransmission in the gastrointestinal tract.

作者信息

Sanders K M

机构信息

Department of Physiology and Cell Biology, University of Nevada School of Medicine, Reno, USA.

出版信息

Gastroenterology. 1996 Aug;111(2):492-515. doi: 10.1053/gast.1996.v111.pm8690216.

Abstract

Electrical rhythmicity in gastrointestinal muscles has been studied for a century, but the pacemakers driving this phenomenon have been elusive. Anatomic studies suggest that interstitial cells of Cajal (ICC) may be pacemakers and conductors of electrical activity. ICC may also mediate neurotransmission from enteric neurons. Functional evaluations of ICC include the following. (1) Electrophysiology experiments on dissected muscle strips show that slow waves originate from specific sites. These pacemaker areas are populated by networks of ICC that make gap junctions with smooth muscle cells. Removal of pacemaker regions interferes with slow wave generation and propagation. (2) Chemicals that label ICC histochemically can damage ICC and abolish rhythmicity. (3) isolated ICC are spontaneously active, and several voltage-dependent ion channels, including a low-threshold Ca2+ conductance, are expressed. (4) ICC are innervated by enteric neurons, and they respond to neurotransmitters. ICC may produce nitric oxide and amplify inhibitory neurotransmission. (5) Some classes of ICC fall to develop in animals with mutations in c-kit or stem cell factor, the ligand for c-Kit receptors. Without ICC, electrical slow waves are absent. Many questions remain about the function of ICC, but modern technologies should now facilitate rapid progress toward determining the role of these cells in normal physiology and pathological conditions.

摘要

胃肠肌肉的电节律性已被研究了一个世纪,但驱动这一现象的起搏器一直难以捉摸。解剖学研究表明, Cajal间质细胞(ICC)可能是电活动的起搏器和传导者。ICC也可能介导来自肠神经元的神经传递。对ICC的功能评估如下:(1)对分离的肌条进行的电生理学实验表明,慢波起源于特定部位。这些起搏区域由与平滑肌细胞形成缝隙连接的ICC网络构成。去除起搏区域会干扰慢波的产生和传播。(2)用组织化学方法标记ICC的化学物质会损伤ICC并消除节律性。(3)分离出的ICC具有自发活性,并且表达几种电压依赖性离子通道,包括低阈值Ca2+电导。(4)ICC由肠神经元支配,并且它们对神经递质有反应。ICC可能产生一氧化氮并放大抑制性神经传递。(5)在c-kit或干细胞因子(c-Kit受体的配体)发生突变的动物中,某些类型的ICC无法发育。没有ICC,电慢波就不存在。关于ICC的功能仍有许多问题,但现代技术现在应该有助于在确定这些细胞在正常生理和病理状况中的作用方面取得快速进展。

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