Hippo通路调控机械力作用下皮肤表皮细胞增殖

IF 5.3
Joanna K. Ledwon, Bianka Progri, Sarah A. Applebaum, Oveyaa Vignesh, Alice Yau, Angie H. Aguilar, Adrian B. Tepole, Arun K. Gosain
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引用次数: 0

摘要

组织扩张是用于促进原生皮肤生长的重建手术的一个组成部分。这个过程是由皮下放置在病人身体上的组织扩张器逐渐膨胀驱动的。尽管它被广泛使用,但缺乏关于皮肤生长背后的生物过程的体内证据,限制了技术的进步。在这里,我们探索在组织扩张过程中控制机械诱导皮肤生长的基因和蛋白质表达变化。利用猪组织扩张模型,我们发现皮肤扩张破坏了负责上皮完整性的关键成分,与未扩张的对照组相比,扩张皮肤中E-cadherin和α -catenin的表达缺失就是证据。这种破坏与转录因子YAP1从膜到细胞核的易位有关,激活角质细胞增殖,并可能调节皮肤适应机械拉伸的其他关键过程。我们的数据表明,体内细胞增殖是由E-cadherin、α -catenin和YAP1组成的分子复合物的力诱导变化介导的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Hippo Pathway Regulates Cell Proliferation in Skin Epidermis Exposed to Mechanical Forces

Hippo Pathway Regulates Cell Proliferation in Skin Epidermis Exposed to Mechanical Forces

Tissue expansion is an integral component of reconstructive surgery used to promote native skin growth. This process is driven by the gradual inflation of the tissue expander placed subcutaneously on the patient's body. Despite its widespread use, the lack of in vivo evidence on the biological processes underlying skin growth has limited technological advancements. Here, we explore the gene and protein expression changes that control mechanically induced skin growth during tissue expansion. Using a porcine tissue expansion model, we revealed that skin expansion disrupts key components responsible for epithelial integrity, as evidenced by the loss of E-cadherin and alpha-catenin expression in expanded skin compared to the unexpanded control. This disruption correlates with the translocation of the transcriptional factor YAP1 from the membrane to the nucleus, activating keratinocyte proliferation and possibly regulating other critical processes involved in skin adaptation to mechanical stretch. Our data show that in vivo cell proliferation is mediated by force-induced changes in the composition of molecular complexes formed by E-cadherin, alpha-catenin, and YAP1.

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来源期刊
CiteScore
11.50
自引率
0.00%
发文量
0
期刊介绍: The Journal of Cellular and Molecular Medicine serves as a bridge between physiology and cellular medicine, as well as molecular biology and molecular therapeutics. With a 20-year history, the journal adopts an interdisciplinary approach to showcase innovative discoveries. It publishes research aimed at advancing the collective understanding of the cellular and molecular mechanisms underlying diseases. The journal emphasizes translational studies that translate this knowledge into therapeutic strategies. Being fully open access, the journal is accessible to all readers.
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