Vinculin和c- cl -associated protein (CAP)抑制Meflin的表达,调节间充质干细胞的刚度依赖性成骨分化。

IF 3.5 3区 生物学 Q3 CELL BIOLOGY
Moe Fujiwara , Akihisa Ogawa , Shinsuke Takahashi , Takeshi Kobayashi , Shuhei Tanabe , Merisa Hosotani , Yasuhisa Kimura , Atsushi Enomoto , Mito Kuroda , Noriyuki Kioka
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引用次数: 0

摘要

Vinculin和c- cl -associated protein (CAP)通过细胞外基质(ECM)的刚度介导间充质干细胞(MSC)分化的调节;然而,vinculin-CAP下游的分子机制尚未完全阐明。在这里,我们证明了vinculin和CAP抑制Meflin的表达,而Meflin是维持MSCs处于未分化状态的关键因素。血管素和CAP的消耗增加了Meflin的表达,特别是在刚性ECM底物上。这种调节通过yes相关蛋白发生,yes相关蛋白是一种影响细胞分化的转录共激活因子。此外,cap介导的Meflin抑制促进刚性ECM上成骨细胞的分化。总体而言,本研究表明,vinculin-CAP-Meflin轴参与了一个复杂的调节机制,该机制根据ECM刚度控制MSC向成骨细胞的分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Vinculin and c-Cbl-associated protein (CAP) suppress Meflin expression to regulate stiffness-dependent osteogenic differentiation of mesenchymal stem cells
Vinculin and c-Cbl-associated protein (CAP) mediate the regulation of mesenchymal stem cell (MSC) differentiation depending on the stiffness of the extracellular matrix (ECM); however, the molecular mechanism downstream of vinculin-CAP is not fully elucidated. Here, we demonstrated that vinculin and CAP suppress Meflin expression, a factor crucial for maintaining MSCs in an undifferentiated state. Depletion of vinculin and CAP increases Meflin expression, particularly on rigid ECM substrates. This regulation occurs through Yes-associated protein, a transcriptional co-activator that influences cellular differentiation. Furthermore, CAP-mediated suppression of Meflin promotes osteoblast differentiation on rigid ECM. Overall, this study demonstrates that the vinculin-CAP-Meflin axis is involved in a complex regulatory mechanism that controls MSC differentiation into osteoblasts depending on ECM stiffness.
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来源期刊
Experimental cell research
Experimental cell research 医学-细胞生物学
CiteScore
7.20
自引率
0.00%
发文量
295
审稿时长
30 days
期刊介绍: Our scope includes but is not limited to areas such as: Chromosome biology; Chromatin and epigenetics; DNA repair; Gene regulation; Nuclear import-export; RNA processing; Non-coding RNAs; Organelle biology; The cytoskeleton; Intracellular trafficking; Cell-cell and cell-matrix interactions; Cell motility and migration; Cell proliferation; Cellular differentiation; Signal transduction; Programmed cell death.
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