可编程和可逆的整合素介导细胞粘附揭示了动因动学的歇斯底里,改变了随后的机械传导
Zheng Zhang1,2, Hongyuan Zhu1,2, Guoqing Zhao1,2
1The Key Laboratory of Biomedical Information Engineering of Ministry of Education, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, 710049, P. R. China.
Advanced science (Weinheim, Baden-Wurttemberg, Germany)
|October 18, 2023
概括
循环细胞粘附动态地改变了人类细胞间干细胞感知细胞外矩阵刚性的方式. F-actin中的这种记忆效应改变了细胞反应,与静态基质结果不同.
科学领域:
- 细胞生物学 细胞生物学
- 生物物理学的生物物理.
- 生物材料科学 生物材料科学
背景情况:
- 细胞对细胞外基质 (ECM) 的粘附和ECM的刚性动态调节细胞机械感知.
- 由于难以单独控制这些因素,因此对这些因素的独立表征具有挑战性.
研究的目的:
- 开发一种用于独立控制动态细胞粘附和ECM刚性的新系统.
- 研究周期性细胞粘附对细胞机械感知的独特影响.
主要方法:
- 一个由DNA驱动的分子系统被设计成可逆地呈现RGD连接体,用于控制细胞的附着和分离.
- 使用这个系统,在具有定义刚性的基板上进行了实验.
- 人类介质干细胞 (hMSCs) 用于研究细胞骨动力学和核机械感知.
主要成果:
- 发现循环细胞粘附加速了hMSCs中的F-actin动力学和核机械感知.
- 观察到细胞响应中的歇斯底里症,显著改变了hMSCs如何转化ECM刚性.
- 结果与静态基板的既定机械传导模型有所不同.
结论:
- 循环整合素介导的粘附引入了一个短暂的歇斯底里记忆,进入hMSCs的ECM刚性的机械感知.
- 这种可能存储在F-actin结构中的记忆,与静态粘附条件相比,导致不同的细胞反应.
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