通过抑制真核细胞翻译起始因子2 α的去磷酸化促进成骨细胞的形成和抑制破骨细胞的形成。

Kazunori Hamamura, Andy Chen, Hiroki Yokota
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引用次数: 6

摘要

真核生物翻译起始因子2α (eIF2α)的磷酸化被激活,以响应各种应激,如病毒感染、营养剥夺和内质网应激。例如,内质网的严重应激诱导凋亡途径,而轻度应激则相反,导致促生存途径。关于eIF2α磷酸化在成骨细胞和骨吸收破骨细胞发育中的复杂作用,我们知之甚少。我们使用salubrinal和guanabenz作为eIF2α去磷酸化的抑制剂,最近报道了eIF2α的磷酸化显著改变了成骨细胞和破骨细胞的命运。基于我们最近的发现,我们在本研究中回顾了通过提高磷酸化的eIF2α水平来增强成骨细胞形成和抑制破骨细胞形成的潜在机制。
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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Enhancement of osteoblastogenesis and suppression of osteoclastogenesis by inhibition of de-phosphorylation of eukaryotic translation initiation factor 2 alpha.

The phosphorylation of eukaryotic translation initiation factor 2 alpha (eIF2α) is activated in response to various stresses such as viral infection, nutrient deprivation, and stress to the endoplasmic reticulum. Severe stress to the endoplasmic reticulum, for instance, induces an apoptotic pathway, while mild stress, on the contrary, leads to a pro-survival pathway. Little has been known about the elaborate role of eIF2α phosphorylation in the development of bone-forming osteoblasts and bone-resorbing osteoclasts. Using salubrinal and guanabenz as inhibitors of the de-phosphorylation of eIF2α, we have recently reported that the phosphorylation of eIF2α significantly alters fates of both osteoblasts and osteoclasts. Based on our recent findings, we review in this research highlight the potential mechanisms of the enhancement of osteoblastogenesis and the suppression of osteoclastogenesis through the elevated level of phosphorylated eIF2α.

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