Journal article
Glucocorticoids alleviate intestinal ER stress by enhancing protein folding and degradation of misfolded proteins
I Das, CW Png, I Oancea, SZ Hasnain, R Lourie, M Proctor, RD Eri, Y Sheng, DI Crane, TH Florin, MA McGuckin
Journal of Experimental Medicine | ROCKEFELLER UNIV PRESS | Published : 2013
DOI: 10.1084/jem.20121268
Abstract
Endoplasmic reticulum (ER) stress in intestinal secretory cells has been linked with colitis in mice and inflammatory bowel disease (IBD). Endogenous intestinal glucocorticoids are important for homeostasis and glucocorticoid drugs are efficacious in IBD. In Winnie mice with intestinal ER stress caused by misfolding of the Muc2 mucin, the glucocorticoid dexamethasone (DEX) suppressed ER stress and activation of the unfolded protein response (UPR), substantially restoring goblet cell Muc2 production. In mice lacking inflammation, a glucocorticoid receptor antagonist increased ER stress, and DEX suppressed ER stress induced by the N-glycosylation inhibitor, tunicamycin (Tm). In cultured human ..
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Awarded by National Health and Medical Research Council
Funding Acknowledgements
This research was supported by National Health and Medical Research Council (NHMRC) Project Grant 488809. I. Das is supported by Griffith University Postgraduate Research Scholarship and Griffith University International Postgraduate Research Scholarship scholarships. T. Florin and M. McGuckin are supported by NHMRC Practitioner and Senior Research Fellowships, respectively.