Effect of complementary relationship between hypoxia-inducible factor-1 and aryl hydrocarbon receptor on intestinal barrier

Author(s)
곽민규
Advisor
장선영
Department
일반대학원 약학과
Publisher
The Graduate School, Ajou University
Publication Year
2021-08
Language
eng
Keyword
Aryl hydrocarbon receptorsGut barrierHypoxia-inducible factor-1Inflammatory bowel disease
Alternative Abstract
The exact cause of inflammatory bowel disease is unknown, and the breakdown of the intestinal barrier causes the leaky gut syndrome. Hypoxia-inducing factors (HIF) and aryl hydrocarbon receptors (AhR) are known to be important factors in maintaining intestinal barrier homeostasis. Organoids and animal models were used to study the effects of HIF and AhR on the intestinal barrier. Stabilizing of HIF increased cell proliferation and increased junctional molecule expression. Organoid size and budding were increased. Barrier integrity in mice was no change after stabilizing of HIF. AhR deficient organoid was generated from the small intestine of AhR deficient mice. Depletion of aryl hydrocarbon receptors resulted in increased cell proliferation and altered intestinal permeability. Immunofluorescence staining showed increased size and budding. AhR deficient intestine had increased permeability, serum endotoxin, and bacterial translocation compared with wild type intestine. Stabilization of HIF in AhR deficient organoids restored intestinal permeability. AhR deficient mice treated with HIF stabilizer decreased endotoxin concentrations and bacterial translocation. Therefore, the increased intestinal permeability due to AhR deficiency can be restored by stabilization of HIF. This has the potential to contribute to the treatment of patients with inflammatory bowel disease and colorectal cancer.
URI
https://dspace.ajou.ac.kr/handle/2018.oak/20405
Fulltext

Appears in Collections:
Graduate School of Ajou University > Department of Pharmacy > 3. Theses(Master)
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

Browse