4.6 Article

Cyclic nucleotides, gut physiology and inflammation

Journal

FEBS JOURNAL
Volume 287, Issue 10, Pages 1970-1981

Publisher

WILEY
DOI: 10.1111/febs.15198

Keywords

cAMP; cGMP; cholera toxin; inflammasome; receptor guanylyl cyclase C; salmonellosis

Funding

  1. Margdarshi Fellowship from the DBT/Wellcome Trust India Alliance [IA/M/16/1/50260621/06/2017]
  2. JC Bose Fellowship from the Department of Science and Technology, Government of India [SB/S2/JCB-18/2013]
  3. Medical Research Council, UK [MR/P022138/1]
  4. MRC [MR/P022138/1, MR/P028225/1] Funding Source: UKRI

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Misregulation of gut function and homeostasis impinges on the overall well-being of the entire organism. Diarrheal disease is the second leading cause of death in children under 5 years of age, and globally, 1.7 billion cases of childhood diarrhea are reported every year. Accompanying diarrheal episodes are a number of secondary effects in gut physiology and structure, such as erosion of the mucosal barrier that lines the gut, facilitating further inflammation of the gut in response to the normal microbiome. Here, we focus on pathogenic bacteria-mediated diarrhea, emphasizing the role of cyclic adenosine 3',5'-monophosphate and cyclic guanosine 3 ',5 '-monophosphate in driving signaling outputs that result in the secretion of water and ions from the epithelial cells of the gut. We also speculate on how this aberrant efflux and influx of ions could modulate inflammasome signaling, and therefore cell survival and maintenance of gut architecture and function.

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