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Piezo 型机械敏感性离子通道成分 1 作为间充质干细胞命运决定的调节因子发挥作用。

Piezo type mechanosensitive ion channel component 1 functions as a regulator of the cell fate determination of mesenchymal stem cells.

机构信息

Department of Pediatric Dentistry, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, 770-8504, Japan.

Support Center for Advanced Medical Sciences, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, 770-8504, Japan.

出版信息

Sci Rep. 2017 Dec 18;7(1):17696. doi: 10.1038/s41598-017-18089-0.

Abstract

The extracellular environment regulates the dynamic behaviors of cells. However, the effects of hydrostatic pressure (HP) on cell fate determination of mesenchymal stem cells (MSCs) are not clearly understood. Here, we established a cell culture chamber to control HP. Using this system, we found that the promotion of osteogenic differentiation by HP is depend on bone morphogenetic protein 2 (BMP2) expression regulated by Piezo type mechanosensitive ion channel component 1 (PIEZO1) in MSCs. The PIEZO1 was expressed and induced after HP loading in primary MSCs and MSC lines, UE7T-13 and SDP11. HP and Yoda1, an activator of PIEZO1, promoted BMP2 expression and osteoblast differentiation, whereas inhibits adipocyte differentiation. Conversely, PIEZO1 inhibition reduced osteoblast differentiation and BMP2 expression. Furthermore, Blocking of BMP2 function by noggin inhibits HP induced osteogenic maker genes expression. In addition, in an in vivo model of medaka with HP loading, HP promoted caudal fin ray development whereas inhibition of piezo1 using GsMTx4 suppressed its development. Thus, our results suggested that PIEZO1 is responsible for HP and could functions as a factor for cell fate determination of MSCs by regulating BMP2 expression.

摘要

细胞外环境调节细胞的动态行为。然而,静水压力 (HP) 对间充质干细胞 (MSC) 命运决定的影响尚不清楚。在这里,我们建立了一个细胞培养室来控制 HP。使用该系统,我们发现 HP 促进成骨分化依赖于 MSC 中由 Piezo 型机械敏感离子通道成分 1 (PIEZO1) 调节的骨形态发生蛋白 2 (BMP2) 表达。PIEZO1 在原代 MSC 和 MSC 系 UE7T-13 和 SDP11 受压后表达并诱导。HP 和 Yoda1(PIEZO1 的激活剂)促进 BMP2 表达和成骨细胞分化,而抑制脂肪细胞分化。相反,PIEZO1 抑制减少成骨细胞分化和 BMP2 表达。此外,BMP2 功能的阻断 noggin 抑制 HP 诱导的成骨标志物基因表达。此外,在 HP 加载的斑马鱼体内模型中,HP 促进尾鳍射线发育,而使用 GsMTx4 抑制 piezo1 抑制其发育。因此,我们的结果表明 PIEZO1 负责 HP,并可通过调节 BMP2 表达作为 MSC 细胞命运决定的因素。

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