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单细胞人β细胞的拟时排序揭示了胰岛素产生和未折叠蛋白反应的状态。

Pseudotime Ordering of Single Human β-Cells Reveals States of Insulin Production and Unfolded Protein Response.

机构信息

Regeneron Pharmaceuticals, Tarrytown, NY.

Regeneron Pharmaceuticals, Tarrytown, NY

出版信息

Diabetes. 2018 Sep;67(9):1783-1794. doi: 10.2337/db18-0365. Epub 2018 Jun 27.

Abstract

Proinsulin is a misfolding-prone protein, making its biosynthesis in the endoplasmic reticulum (ER) a stressful event. Pancreatic β-cells overcome ER stress by activating the unfolded protein response (UPR) and reducing insulin production. This suggests that β-cells transition between periods of high insulin biosynthesis and UPR-mediated recovery from cellular stress. We now report the pseudotime ordering of single β-cells from humans without diabetes detected by large-scale RNA sequencing. We identified major states with ) low UPR and low insulin gene expression, ) low UPR and high insulin gene expression, or ) high UPR and low insulin gene expression. The latter state was enriched for proliferating cells. Stressed human β-cells do not dedifferentiate and show little propensity for apoptosis. These data suggest that human β-cells transition between states with high rates of biosynthesis to fulfill the body's insulin requirements to maintain normal blood glucose levels and UPR-mediated recovery from ER stress due to high insulin production.

摘要

胰岛素原是一种易于错误折叠的蛋白质,因此其在内质网(ER)中的生物合成是一个应激事件。胰腺β细胞通过激活未折叠蛋白反应(UPR)并减少胰岛素的产生来克服 ER 应激。这表明β细胞在高胰岛素生物合成和 UPR 介导的细胞应激恢复之间交替。我们现在报告了通过大规模 RNA 测序检测到的来自无糖尿病的人类的单个β细胞的伪时间排序。我们确定了主要状态,包括)低 UPR 和低胰岛素基因表达,)低 UPR 和高胰岛素基因表达,或)高 UPR 和低胰岛素基因表达。后一种状态富含增殖细胞。应激的人β细胞不会去分化,并且很少表现出凋亡的倾向。这些数据表明,人β细胞在高生物合成率的状态之间转换,以满足身体对胰岛素的需求,从而维持正常的血糖水平,并通过 UPR 介导的恢复来应对由于高胰岛素产生而导致的 ER 应激。

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