Author:
Jimenez Isabel A.,Stilin Allison P.,Morohaku Kanako,Hussein Mahmoud H.,Koganti Prasanthi P.,Selvaraj Vimal
Abstract
In human patients and animal models of ulcerative colitis (UC), upregulation of the mitochondrial translocator protein (TSPO) in the colon is consistent with inflammation. Although the molecular function for TSPO remains unclear, it has been investigated as a therapeutic target for ameliorating UC pathology. In this study, we examined the susceptibility ofTspogene-deleted (Tspo−/−) mice to insults as provided by the dextran sodium sulfate (DSS)-induced acute UC model. Our results show that UC clinical signs and pathology were severely exacerbated inTspo−/−mice compared to controlTspofl/flcohorts. Histopathology showed extensive inflammation and epithelial loss inTspo−/−mice that caused an aggravated disease. Colonic gene expression in UC uncovered an etiology linked to precipitous loss of epithelial integrity and disproportionate mast cell activation assessed by tryptase levels inTspo−/−colons. Evaluation of baseline homeostatic shifts inTspo−/−colons revealed gene expression changes noted in elevated epithelialCdx2, mast cellCd36andMcp6, with general indicators of lower proliferation capacity and elevated mitochondrial fatty acid oxidation. These findings demonstrate that intact physiological TSPO function serves to limit inflammation in acute UC, and provide a systemic basis for investigating TSPO-targeting mechanistic therapeutics.
Funder
National Institute of Diabetes and Digestive and Kidney Diseases
Subject
Physiology (medical),Physiology
Cited by
1 articles.
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