Interactions Between Autophagy and the Unfolded Protein Response: Implications for Inflammatory Bowel Disease

被引:33
作者
Hooper, Kirsty M. [1 ]
Barlow, Peter G. [1 ]
Henderson, Paul [2 ,3 ]
Stevens, Craig [1 ]
机构
[1] Edinburgh Napier Univ, Sch Appl Sci, Sighthill Campus, Edinburgh EH11 4BN, Midlothian, Scotland
[2] Univ Edinburgh, Child Life & Hlth, Edinburgh, Midlothian, Scotland
[3] Royal Hosp Sick Children, Dept Paediat Gastroenterol & Nutr, Edinburgh, Midlothian, Scotland
关键词
IBD; autophagy; unfolded protein response; ER stress; ENDOPLASMIC-RETICULUM STRESS; GENOME-WIDE ASSOCIATION; XBP1; MESSENGER-RNA; LINKS ER STRESS; CROHNS-DISEASE; TRANSCRIPTION FACTOR; KAPPA-B; TRANSMEMBRANE PROTEIN; CHEMICAL CHAPERONES; SIROLIMUS RAPAMYCIN;
D O I
10.1093/ibd/izy380
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Inflammatory bowel disease (IBD), which includes Crohn's disease (CD) and ulcerative colitis, is characterized by chronic inflammation of the gastrointestinal tract. The etiology involves a combination of genetic and environmental factors resulting in abnormal immune responses to intestinal microbiota. Genetic studies have strongly linked genes involved in autophagy to CD, and genes involved in the unfolded protein response (UPR) to IBD. The UPR is triggered in response to accumulation of misfolded proteins in the endoplasmic reticulum (ER), and autophagy plays a key role in relieving ER stress and restoring homeostasis. This review summarizes the known interactions between autophagy and the UPR and discusses the impact of these converging pathways on IBD pathogenesis. With a paucity of effective long-term treatments for IBD, targeting of synergistic pathways may provide novel and more effective therapeutic options.
引用
收藏
页码:661 / 671
页数:11
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