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粘着斑激酶和p130Cas调节硬度介导的早期转录和细胞代谢。

FAK and p130Cas Modulate Stiffness-Mediated Early Transcription and Cellular Metabolism.

作者信息

Tumenbayar Bat-Ider, Pham Khanh, Biber John C, Tutino Vincent M, Brazzo Joseph A, Yao Peng, Bae Yongho

机构信息

Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York, USA.

Department of Pathology and Anatomical Sciences, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, Buffalo, New York, USA.

出版信息

Cytoskeleton (Hoboken). 2025 Mar;82(3):197-215. doi: 10.1002/cm.21971. Epub 2024 Dec 9.

Abstract

Cellular metabolism is influenced by the stiffness of the extracellular matrix. Focal adhesion kinase (FAK) and its binding partner, p130Cas, transmit biomechanical signals, such as substrate stiffness, to the cell to regulate a variety of cellular responses, but their roles in early transcriptional and metabolic responses remain largely unexplored. We cultured mouse embryonic fibroblasts with or without siRNA-mediated FAK or p130Cas knockdown and assessed the early transcriptional responses of these cells to placement on soft and stiff substrates by RNA sequencing and bioinformatics analyses. Exposure to the stiff substrate altered the expression of genes important for metabolic and biosynthetic processes, and these responses were influenced by knockdown of FAK and p130Cas. Our findings reveal that FAK-p130Cas signaling mechanotransduces substrate stiffness to early transcriptional changes that alter cellular metabolism and biosynthesis.

摘要

细胞代谢受细胞外基质硬度的影响。粘着斑激酶(FAK)及其结合伴侣p130Cas将生物力学信号(如底物硬度)传递给细胞,以调节多种细胞反应,但其在早期转录和代谢反应中的作用在很大程度上仍未得到探索。我们用或不用小干扰RNA介导的FAK或p130Cas基因敲低培养小鼠胚胎成纤维细胞,并通过RNA测序和生物信息学分析评估这些细胞置于柔软和坚硬底物上后的早期转录反应。暴露于坚硬底物会改变对代谢和生物合成过程重要的基因的表达,而这些反应受FAK和p130Cas基因敲低的影响。我们的研究结果表明,FAK-p130Cas信号转导机制将底物硬度转化为早期转录变化,从而改变细胞代谢和生物合成。

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