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肠道稳态中细菌调节的信号通路。

Bacterial-modulated signaling pathways in gut homeostasis.

作者信息

Lee Won-Jae

机构信息

Division of Life and Pharmaceutical Science and Department of Life Science, Ewha Woman's University, and National Creative Research Initiative Center for Symbiosystem, Seoul 120-750, South Korea.

出版信息

Sci Signal. 2008 May 27;1(21):pe24. doi: 10.1126/stke.121pe24.

Abstract

Symbiotic mutualism with gut microbes occurs in all metazoans, and it is well established that commensal bacteria influence multiple aspects of host gut physiology such as innate immunity and development. However, our understanding of these coevolved interactions between prokaryotes and eukaryotes remains unclear. One mechanism by which commensal bacteria modulate host intracellular signaling pathways in order to avoid excess inflammation has now been determined. In this process, bacterial-induced reactive oxygen species in gut epithelial cells act as key messengers that inhibit the cullin-1-dependent protein degradation machinery, which in turn results in the stabilization of a master negative regulator of inflammation, inhibitor of nuclear factor-kappaB (IkappaB). Furthermore, this bacterial-mediated system also appears to be involved in the stabilization of a key developmental regulator, beta-catenin. These findings provide new insights into the molecular mechanisms by which commensal microbes shape host cellular physiology.

摘要

与肠道微生物的共生互利关系存在于所有后生动物中,并且共生细菌影响宿主肠道生理学的多个方面,如固有免疫和发育,这一点已得到充分证实。然而,我们对原核生物与真核生物之间这些共同进化的相互作用的理解仍不清楚。现在已经确定了共生细菌调节宿主细胞内信号通路以避免过度炎症的一种机制。在此过程中,肠道上皮细胞中细菌诱导的活性氧作为关键信使,抑制依赖cullin-1的蛋白质降解机制,这反过来又导致炎症的主要负调节因子核因子κB抑制蛋白(IkappaB)的稳定。此外,这种细菌介导的系统似乎也参与了关键发育调节因子β-连环蛋白的稳定。这些发现为共生微生物塑造宿主细胞生理学的分子机制提供了新的见解。

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