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环核苷酸、肠道生理学与炎症。

Cyclic nucleotides, gut physiology and inflammation.

机构信息

Department of Molecular Reproduction, Development and Genetics, Indian Institute of Science, Bengaluru, India.

Medical Research Council Centre for Molecular Bacteriology and Infection, Imperial College London, UK.

出版信息

FEBS J. 2020 May;287(10):1970-1981. doi: 10.1111/febs.15198. Epub 2020 Jan 14.

Abstract

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.

摘要

肠道功能和稳态的失调会影响整个生物体的整体健康。腹泻病是 5 岁以下儿童死亡的第二大原因,全球每年报告有 17 亿例儿童腹泻病。腹泻伴随的还有一系列肠道生理和结构的继发效应,如肠道衬里的黏膜屏障被侵蚀,这使得肠道对正常微生物组的进一步炎症反应更加容易。在这里,我们重点关注致病性细菌引起的腹泻,强调环腺苷酸 3',5'-单磷酸和环鸟苷酸 3',5'-单磷酸在驱动信号输出中的作用,这些信号输出导致肠道上皮细胞分泌水和离子。我们还推测这种异常的离子流出和流入如何调节炎症小体信号,从而影响细胞存活和维持肠道结构和功能。

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