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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Roles of connexins and pannexins in digestive homeostasis

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Author(s):
Maes, Michael [1] ; Cogliati, Bruno [2] ; Yanguas, Sara Crespo [1] ; Willebrords, Joost [1] ; Vinken, Mathieu [1]
Total Authors: 5
Affiliation:
[1] Vrije Univ Brussel, Dept Vitro Toxicol & Dermatocosmetol, B-1090 Brussels - Belgium
[2] Univ Sao Paulo, Sch Vet Med & Anim Sci, Dept Pathol, Sao Paulo - Brazil
Total Affiliations: 2
Document type: Review article
Source: CELLULAR AND MOLECULAR LIFE SCIENCES; v. 72, n. 15, p. 2809-2821, AUG 2015.
Web of Science Citations: 12
Abstract

Connexin proteins are abundantly present in the digestive system. They primarily form gap junctions, which control the intercellular exchange of critical homeostasis regulators. By doing so, gap junctions drive a plethora of gastrointestinal and hepatic functional features, including gastric and gut motility, gastric acid secretion, intestinal innate immune defense, xenobiotic biotransformation, glycogenolysis, bile secretion, ammonia detoxification and plasma protein synthesis. In the last decade, it has become clear that connexin hemichannels, which are the structural precursors of gap junctions, also provide a pathway for cellular communication, namely between the cytosol and the extracellular environment. Although merely pathological functions have been described, some physiological roles have been attributed to connexin hemichannels, in particular in the modulation of colonic motility. This equally holds true for cellular channels composed of pannexins, connexin-like proteins recently identified in the intestine and the liver, which have become acknowledged key players in inflammatory processes and that have been proposed to control colonic motility, secretion and blood flow. (AU)

FAPESP's process: 13/50420-6 - Connexin and pannexin channels as drug targets and biomarkers in acute and chronic liver disease
Grantee:Mathieu Frederick Alexander Vinken
Support Opportunities: Research Projects - SPEC Program