Regulation of TWIK-related potassium channel-1 (Trek1) restitutes intestinal epithelial barrier function.

Abstract:

:The disruption of epithelial barrier integrity is an important factor in the pathogenesis of various immune disorders. However, the restitution of the compromised barrier functions is difficult. This study investigates the regulation of TWIK-related potassium channel-1 (Trek1) in the restitution of intestinal epithelial barrier functions. The human colon epithelial cell line T84 was cultured in monolayers and used to observe epithelial barrier functions in vitro. An intestinal allergy mouse model was created. Cytokine levels were determined by enzyme-linked immunosorbent assay and western blotting. The results showed that Trek1 deficiency induced T84 monolayer barrier disruption. Allergic responses markedly suppressed the expression of Trek1 in the intestinal epithelia via activating the mitogen-activated protein kinase pathways and increasing the expression of histone deacetylase-1. The inhibition of histone deacetylase-1 by sodium butyrate or the administration of a butyrate-producing probiotic (Clostridium butyricum) restored the intestinal epithelial barrier functions and markedly enhanced the effect of antigen-specific immunotherapy. The data suggest that Trek1 is required for the maintenance of intestinal epithelial barrier integrity. Allergic responses induce an insufficiency of Trek1 expression in the intestinal epithelia. Trek1 expression facilitates the restoration of intestinal epithelial barrier functions in an allergic environment.

journal_name

Cell Mol Immunol

authors

Huang H,Liu JQ,Yu Y,Mo LH,Ge RT,Zhang HP,Liu ZG,Zheng PY,Yang PC

doi

10.1038/cmi.2014.137

subject

Has Abstract

pub_date

2016-01-01 00:00:00

pages

110-8

issue

1

eissn

1672-7681

issn

2042-0226

pii

cmi2014137

journal_volume

13

pub_type

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