Slc26a3 (DRA) in the Gut: Expression, Function, Regulation, Role in Infectious Diarrhea and Inflammatory Bowel Disease

Inflamm Bowel Dis. 2021 Mar 15;27(4):575-584. doi: 10.1093/ibd/izaa256.

Abstract

Background: The transport of transepithelial Cl- and HCO3- is crucial for the function of the intestinal epithelium and maintains the acid-based homeostasis. Slc26a3 (DRA), as a key chloride-bicarbonate exchanger protein in the intestinal epithelial luminal membrane, participates in the electroneutral NaCl absorption of intestine, together with Na+/H+ exchangers. Increasing recent evidence supports the essential role of decreased DRA function or expression in infectious diarrhea and inflammatory bowel disease (IBD).

Method: In this review, we give an overview of the current knowledge of Slc26a3, including its cloning and expression, function, roles in infectious diarrhea and IBD, and mechanisms of actions. A better understanding of the physiological and pathophysiological relevance of Slc26a3 in infectious diarrhea and IBD may reveal novel targets for future therapy.

Conclusion: Understanding the physiological function, regulatory interactions, and the potential mechanisms of Slc26a3 in the pathophysiology of infectious diarrhea and IBD will define novel therapeutic approaches in future.

Keywords: DRA; Slc26a3; expression; function; infectious diarrhea; inflammatory bowel disease; regulation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Chloride-Bicarbonate Antiporters* / genetics
  • Diarrhea* / genetics
  • Humans
  • Inflammatory Bowel Diseases* / genetics
  • Intestinal Mucosa
  • Sodium-Hydrogen Exchangers
  • Sulfate Transporters* / genetics

Substances

  • Chloride-Bicarbonate Antiporters
  • SLC26A3 protein, human
  • Sodium-Hydrogen Exchangers
  • Sulfate Transporters