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内质网应激中未折叠蛋白反应在健康与疾病中的作用的最新见解

Recent Insights into the Role of Unfolded Protein Response in ER Stress in Health and Disease.

作者信息

Lindholm Dan, Korhonen Laura, Eriksson Ove, Kõks Sulev

机构信息

Medicum, Department of Biochemistry and Developmental Biology, Faculty of Medicine, University of HelsinkiHelsinki, Finland.

Minerva Foundation Institute for Medical ResearchHelsinki, Finland.

出版信息

Front Cell Dev Biol. 2017 May 10;5:48. doi: 10.3389/fcell.2017.00048. eCollection 2017.

Abstract

Unfolded stress response (UPR) is a conserved cellular pathway involved in protein quality control to maintain homeostasis under different conditions and disease states characterized by cell stress. Although three general schemes of and genes induced by UPR are rather well-established, open questions remain including the precise role of UPR in human diseases and the interactions between different sensor systems during cell stress signaling. Particularly, the issue how the normally adaptive and pro-survival UPR pathway turns into a deleterious process causing sustained endoplasmic reticulum (ER) stress and cell death requires more studies. UPR is also named a friend with multiple personalities that we need to understand better to fully recognize its role in normal physiology and in disease pathology. UPR interacts with other organelles including mitochondria, and with cell stress signals and degradation pathways such as autophagy and the ubiquitin proteasome system. Here we review current concepts and mechanisms of UPR as studied in different cells and model systems and highlight the relevance of UPR and related stress signals in various human diseases.

摘要

未折叠蛋白反应(UPR)是一种保守的细胞途径,参与蛋白质质量控制,以在不同条件和以细胞应激为特征的疾病状态下维持体内平衡。尽管UPR诱导的三种一般机制和基因已相当明确,但仍存在一些未解决的问题,包括UPR在人类疾病中的精确作用以及细胞应激信号传导过程中不同传感系统之间的相互作用。特别是,正常情况下具有适应性和促生存作用的UPR途径如何转变为导致持续内质网(ER)应激和细胞死亡的有害过程这一问题需要更多研究。UPR也被称为具有多重性格的朋友,我们需要更好地理解它,以便充分认识其在正常生理学和疾病病理学中的作用。UPR与包括线粒体在内的其他细胞器相互作用,并与细胞应激信号以及自噬和泛素蛋白酶体系统等降解途径相互作用。在这里,我们综述了在不同细胞和模型系统中研究的UPR的当前概念和机制,并强调了UPR和相关应激信号在各种人类疾病中的相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9d7e/5423914/3387f0b70edb/fcell-05-00048-g0001.jpg

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