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[肠道上皮中的氯离子分泌:通道、离子与细胞内信号传导]

[Chloride secretion in the intestinal epithelium: channels, ions, and intracellular signaling].

作者信息

Mayol J, Fernández-Represa J A

机构信息

Servicio de Cirugía I, Hospital Clínico San Carlos, Madrid.

出版信息

Rev Esp Enferm Dig. 1998 Oct;90(10):714-21.

PMID:9824937
Abstract

Salt and water secretion by epithelial cells is required to hydrate the mucosal surface of both gastrointestinal and respiratory tracts. Intestinal secretion is the result of active transcellular chloride transport by epithelial cells lining the crypts. Defective chloride secretion is responsible for many common disorders such as secretory diarrhea and cystic fibrosis. In this review we deal with the most relevant issues regarding epithelial transcellular chloride secretion. We first consider the principles of membrane transport and transport protein function. Then, we briefly discuss the use of state-of-the-art techniques for electrophysiological studies such as "patch-clamp" and microfluorometry. The epithelial chloride secretion model is described according to observations made in both native tissue and cultured intestinal epithelial cells. Next, we consider the intracellular signaling cascades involved in the regulation of membrane transport systems and transcellular chloride secretion. Finally, the clinical implications of the most recent findings are commented, with emphasis on potential molecular targets for the treatment of cystic fibrosis and secretory diarrhea.

摘要

上皮细胞分泌盐和水对于胃肠道和呼吸道黏膜表面的水合作用至关重要。肠道分泌是隐窝内衬上皮细胞主动跨细胞转运氯离子的结果。氯离子分泌缺陷是导致许多常见疾病的原因,如分泌性腹泻和囊性纤维化。在这篇综述中,我们探讨了与上皮细胞跨细胞氯离子分泌最相关的问题。我们首先考虑膜转运和转运蛋白功能的原理。然后,我们简要讨论用于电生理研究的前沿技术,如“膜片钳”和显微荧光测定法的应用。根据在天然组织和培养的肠道上皮细胞中的观察结果描述上皮细胞氯离子分泌模型。接下来,我们考虑参与膜转运系统调节和跨细胞氯离子分泌的细胞内信号级联反应。最后,对最新研究结果的临床意义进行了评论,重点关注治疗囊性纤维化和分泌性腹泻的潜在分子靶点。

相似文献

1
[Chloride secretion in the intestinal epithelium: channels, ions, and intracellular signaling].[肠道上皮中的氯离子分泌:通道、离子与细胞内信号传导]
Rev Esp Enferm Dig. 1998 Oct;90(10):714-21.
2
Evidence for intestinal chloride secretion.肠氯离子分泌的证据。
Exp Physiol. 2010 Apr;95(4):471-8. doi: 10.1113/expphysiol.2009.049445.
3
Genistein and tyrphostin 47 stimulate CFTR-mediated Cl- secretion in T84 cell monolayers.染料木黄酮和 tyrphostin 47 刺激 T84 细胞单层中 CFTR 介导的氯离子分泌。
Am J Physiol. 1995 Dec;269(6 Pt 1):G874-82. doi: 10.1152/ajpgi.1995.269.6.G874.
4
The chloride channel ClC-4 co-localizes with cystic fibrosis transmembrane conductance regulator and may mediate chloride flux across the apical membrane of intestinal epithelia.氯离子通道ClC-4与囊性纤维化跨膜传导调节因子共定位,可能介导氯离子通过肠上皮细胞顶端膜的通量。
J Biol Chem. 2002 Jan 4;277(1):566-74. doi: 10.1074/jbc.M106968200. Epub 2001 Oct 23.
5
Evidence that two distinct crypt cell types secrete chloride and potassium in human colon.证据表明,两种不同的隐窝细胞类型在人结肠中分泌氯和钾。
Gut. 2014 Mar;63(3):472-9. doi: 10.1136/gutjnl-2013-304695. Epub 2013 Jun 5.
6
Commentary on 'Evidence for intestinal chloride secretion'.关于“肠道氯离子分泌证据”的评论
Exp Physiol. 2010 Apr;95(4):478-9. doi: 10.1113/expphysiol.2009.051391.
7
Maxi K+ channels co-localised with CFTR in the apical membrane of an exocrine gland acinus: possible involvement in secretion.大电导钙激活钾通道(Maxi K+通道)与囊性纤维化跨膜传导调节因子(CFTR)共定位于外分泌腺腺泡的顶端膜:可能参与分泌过程。
Pflugers Arch. 2001 Apr;442(1):1-11. doi: 10.1007/s004240000493.
8
Activation of intestinal Cl- secretion by lubiprostone requires the cystic fibrosis transmembrane conductance regulator.鲁比前列酮激活肠道氯离子分泌需要囊性纤维化跨膜传导调节因子。
Gastroenterology. 2009 Sep;137(3):976-85. doi: 10.1053/j.gastro.2009.05.037. Epub 2009 May 18.
9
Phenanthrolines--a new class of CFTR chloride channel openers.菲咯啉类——一类新型的囊性纤维化跨膜传导调节因子氯离子通道开放剂。
Br J Pharmacol. 2001 Oct;134(4):853-64. doi: 10.1038/sj.bjp.0704328.
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ClC-2 contributes to native chloride secretion by a human intestinal cell line, Caco-2.氯离子通道蛋白2(ClC-2)有助于人肠道细胞系Caco-2进行天然氯化物分泌。
J Biol Chem. 2001 Mar 16;276(11):8306-13. doi: 10.1074/jbc.M006764200. Epub 2000 Nov 28.

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