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肠道微生物群与未折叠蛋白反应之间的相互作用:对肠道内稳态维持及与生态失调相关疾病的影响。

The interplay between gut microbiota and the unfolded protein response: Implications for intestinal homeostasis preservation and dysbiosis-related diseases.

作者信息

Di Mattia Miriam, Sallese Michele, Lopetuso Loris Riccardo

机构信息

Department of Medicine and Ageing Sciences, "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy; Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy.

Department of Medicine and Ageing Sciences, "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy; Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University of Chieti-Pescara, Chieti, Italy.

出版信息

Microb Pathog. 2025 Mar;200:107279. doi: 10.1016/j.micpath.2025.107279. Epub 2025 Jan 4.

Abstract

The unfolded protein response (UPR) is a complex intracellular signal transduction system that orchestrates the cellular response during Endoplasmic Reticulum (ER) stress conditions to reestablish cellular proteostasis. If, on one side, prolonged ER stress conditions can lead to programmed cell death and autophagy as a cytoprotective mechanism, on the other, unresolved ER stress and improper UPR activation represent a perilous condition able to trigger or exacerbate inflammatory responses. Notably, intestinal and immune cells experience ER stress physiologically due to their high protein secretory rate. Indeed, there is evidence of UPR's involvement in both physiological and pathological intestinal conditions, while less is known about its bidirectional interaction with gut microbiota. However, gut microbes and their metabolites can influence ER stress and UPR pathways, and, in turn, ER stress conditions can shape gut microbiota composition, with important implications for overall intestinal health. Thus, targeting UPR components is an intriguing strategy for treating ER stress-linked dysbiosis and diseases, particularly intestinal inflammation.

摘要

未折叠蛋白反应(UPR)是一种复杂的细胞内信号转导系统,它在内质网(ER)应激条件下协调细胞反应,以重建细胞蛋白质稳态。一方面,长期的内质网应激条件可导致程序性细胞死亡和自噬,作为一种细胞保护机制;另一方面,未解决的内质网应激和不适当的未折叠蛋白反应激活代表一种危险状况,能够引发或加剧炎症反应。值得注意的是,肠道和免疫细胞由于其高蛋白分泌率而在生理上经历内质网应激。事实上,有证据表明未折叠蛋白反应参与了生理和病理肠道状况,而关于其与肠道微生物群的双向相互作用知之甚少。然而,肠道微生物及其代谢产物可影响内质网应激和未折叠蛋白反应途径,反过来,内质网应激条件可塑造肠道微生物群组成,这对整体肠道健康具有重要意义。因此,靶向未折叠蛋白反应成分是治疗内质网应激相关的生态失调和疾病,特别是肠道炎症的一种有趣策略。

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