在MLO-Y4骨细胞中,piezo1介导的流体剪切应力通过NOTCH3促进OPG并抑制RANKL。

Zhongcheng Liu, Yuchen Tang, Liangzhi He, Bin Geng, Fan Lu, Jinwen He, Qiong Yi, Xuening Liu, Kun Zhang, Lifu Wang, Yayi Xia, Jin Jiang
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引用次数: 3

摘要

Piezo1是一种机械敏感离子通道,参与维持骨稳态的多种生物过程。骨细胞是哺乳动物骨骼中最丰富的细胞,在骨形成、骨重塑和骨量维持中起着至关重要的作用。通过将MLO-Y4骨细胞暴露于流体剪切应力(FSS)微环境中,我们探讨了piezo1介导的FSS对骨形成和吸收过程中关键分子、核因子- κ b配体受体激活因子(RANKL)和骨保护素(OPG)表达的影响。结果发现,当MLO-Y4骨细胞暴露于FSS微环境时,9 dyne/cm2加载30分钟后,Piezo1呈上调趋势。FSS促进OPG的表达,抑制RANKL的表达。Piezo1的阻滞剂GsMTx4下调FSS对这两种分子表达的影响。此外,NOTCH3也参与了这一过程。因此,结果表明,piezo1介导的FSS促进了MLO-Y4骨细胞中OPG的表达,并通过NOTCH3抑制RANKL的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Piezo1-mediated fluid shear stress promotes OPG and inhibits RANKL via NOTCH3 in MLO-Y4 osteocytes.

Piezo1-mediated fluid shear stress promotes OPG and inhibits RANKL via NOTCH3 in MLO-Y4 osteocytes.

Piezo1-mediated fluid shear stress promotes OPG and inhibits RANKL via NOTCH3 in MLO-Y4 osteocytes.

Piezo1-mediated fluid shear stress promotes OPG and inhibits RANKL via NOTCH3 in MLO-Y4 osteocytes.

Piezo1, a mechanosensitive ion channel, participates in a variety of biological processes in maintaining bone homeostasis. As the most abundant cells in bones of the mammals, osteocytes play an essential role in bone formation, remodeling, and bone mass maintenance. Here, by exposing MLO-Y4 osteocytes to the fluid shear stress (FSS) microenvironment, we explored the effect of Piezo1-mediated FSS on the expression of the molecules critical to the process of bone formation and resorption, Receptor Activator of Nuclear Factor-Kappa-B Ligand (RANKL) and Osteoprotegerin (OPG). It was found that 9 dyne/cm2 loading for 30 minutes showed an upregulation trend on Piezo1 when MLO-Y4 osteocytes were exposed to an FSS microenvironment. FSS promotes the expression of OPG and inhibits the expression of RANKL. The blocker of Piezo1, GsMTx4, downregulates the effect of FSS on the expression of these two molecules. In addition, NOTCH3 was involved in this process. Thus, the results demonstrated that Piezo1-mediated FSS promotes the expression of OPG and inhibits the expression of RANKL via NOTCH3 in MLO-Y4 osteocytes.

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