[Unfolded protein response in osteoclastogenesis].

Clinical calcium Pub Date : 2016-04-01
Keisuke Horiuchi
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Abstract

Secreted proteins are synthesized and folded to acquire three-dimensional conformation in the endoplasmic reticulum(ER). Accumulation of unfolded proteins in the ER lumen triggers various cellular signals to remove these proteins and normalize the functions of the ER. This cellular mechanism is called the unfolded protein response(UPR)and medicated by three distinct signaling pathways in mammalian cells. Studies over the past decade have revealed that the UPR also has diverse functions that are not necessarily related to the maintenance of the ER. In osteoblasts and chondrocytes, it is now clear that the UPR not only functions to expand the capacity of the ER but also regulates the differentiation of these cells. Furthermore, recent studies suggest that the UPR is induced in osteoclast precursors after RANKL stimulation and has roles in osteoclastogenesis. This short review summarizes the findings of the recent studies on the unconventional roles of the UPR in osteoclast differentiation.

未折叠蛋白在破骨细胞发生中的反应。
分泌的蛋白质在内质网(ER)中合成和折叠以获得三维构象。未折叠的蛋白质在内质网腔内的积累触发各种细胞信号以去除这些蛋白质并使内质网功能正常化。这种细胞机制被称为未折叠蛋白反应(UPR),哺乳动物细胞中有三种不同的信号通路。过去十年的研究表明,普遍定期审议也具有多种功能,这些功能不一定与维持应急机制有关。在成骨细胞和软骨细胞中,UPR不仅可以扩大内质网的容量,还可以调节这些细胞的分化。此外,最近的研究表明,在RANKL刺激后,UPR在破骨细胞前体中被诱导,并在破骨细胞发生中发挥作用。本文就UPR在破骨细胞分化中的非常规作用的最新研究成果进行综述。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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