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肠道微生物群通过内质网应激-自噬-细胞死亡信号轴调节肠道炎症。

Gut microbiota modulate intestinal inflammation by endoplasmic reticulum stress-autophagy-cell death signaling axis.

作者信息

He Feiyang, Zheng Yi, Elsabagh Mabrouk, Fan Kewei, Zha Xia, Zhang Bei, Wang Mengzhi, Zhang Hao

机构信息

Laboratory of Metabolic Manipulation of Herbivorous Animal Nutrition, College of Animal Science and Technology, Yangzhou University, Yangzhou, 225009, P. R. China.

Joint International Research Laboratory of Agriculture and Agri-Product Safety, the Ministry of Education of China, Yangzhou University, Yangzhou, 225009, P. R. China.

出版信息

J Anim Sci Biotechnol. 2025 May 2;16(1):63. doi: 10.1186/s40104-025-01196-8.

Abstract

The intestinal tract, a complex organ responsible for nutrient absorption and digestion, relies heavily on a balanced gut microbiome to maintain its integrity. Disruptions to this delicate microbial ecosystem can lead to intestinal inflammation, a hallmark of inflammatory bowel disease (IBD). While the role of the gut microbiome in IBD is increasingly recognized, the underlying mechanisms, particularly those involving endoplasmic reticulum (ER) stress, autophagy, and cell death, remain incompletely understood. ER stress, a cellular response to various stressors, can trigger inflammation and cell death. Autophagy, a cellular degradation process, can either alleviate or exacerbate ER stress-induced inflammation, depending on the specific context. The gut microbiome can influence both ER stress and autophagy pathways, further complicating the interplay between these processes. This review delves into the intricate relationship between ER stress, autophagy, and the gut microbiome in the context of intestinal inflammation. By exploring the molecular mechanisms underlying these interactions, we aim to provide a comprehensive theoretical framework for developing novel therapeutic strategies for IBD. A deeper understanding of the ER stress-autophagy axis, the gut microbial-ER stress axis, and the gut microbial-autophagy axis may pave the way for targeted interventions to restore intestinal health and mitigate the impact of IBD.

摘要

肠道是一个负责营养吸收和消化的复杂器官,严重依赖平衡的肠道微生物群来维持其完整性。对这种微妙的微生物生态系统的破坏会导致肠道炎症,这是炎症性肠病(IBD)的一个标志。虽然肠道微生物群在IBD中的作用越来越受到认可,但其潜在机制,特别是那些涉及内质网(ER)应激、自噬和细胞死亡的机制,仍未完全了解。内质网应激是细胞对各种应激源的反应,可引发炎症和细胞死亡。自噬是一种细胞降解过程,根据具体情况,它既可以减轻也可以加剧内质网应激诱导的炎症。肠道微生物群可以影响内质网应激和自噬途径,进一步使这些过程之间的相互作用变得复杂。这篇综述深入探讨了在内脏炎症背景下内质网应激、自噬和肠道微生物群之间的复杂关系。通过探索这些相互作用的分子机制,我们旨在为开发IBD的新型治疗策略提供一个全面的理论框架。对内质网应激-自噬轴、肠道微生物-内质网应激轴和肠道微生物-自噬轴的更深入理解可能为恢复肠道健康和减轻IBD影响的靶向干预铺平道路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/566c/12046778/1a74a8c2195b/40104_2025_1196_Fig1_HTML.jpg

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