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重力矢量诱导rMSCs联合底物刚度和取向的机械重塑。

Gravity-Vector Induces Mechanical Remodeling of rMSCs Combined Substrate Stiffness and Orientation.

作者信息

Zhang Chen, Lü Dongyuan, Zhang Fan, Wu Yi, Zheng Lu, Zhang Xiaoyu, Li Zhan, Sun Shujin, Long Mian

机构信息

Center for Biomechanics and Bioengineering, Key Laboratory of Microgravity (National Microgravity Laboratory) and Beijing Key Laboratory of Engineered Construction and Mechanobiology, Institute of Mechanics, Chinese Academy of Sciences, Beijing, China.

School of Engineering Science, University of Chinese Academy of Sciences, Beijing, China.

出版信息

Front Bioeng Biotechnol. 2022 Feb 7;9:724101. doi: 10.3389/fbioe.2021.724101. eCollection 2021.

Abstract

Distinct physical factors originating from the cellular microenvironment are crucial to the biological homeostasis of stem cells. While substrate stiffness and orientation are known to regulate the mechanical remodeling and fate decision of mesenchymal stem cells (MSCs) separately, it remains unclear how the two factors are combined to manipulate their mechanical stability under gravity vector. Here we quantified these combined effects by placing rat MSCs onto stiffness-varied poly-dimethylsiloxane (PDMS) substrates in upward (180°), downward (0°), or edge-on (90°) orientation. Compared with those values onto glass coverslip, the nuclear longitudinal translocation, due to the density difference between the nucleus and the cytosol, was found to be lower at 0° for 24 h and higher at 90° for 24 and 72 h onto 2.5 MPa PDMS substrate. At 0°, the cell was mechanically supported by remarkably reduced actin and dramatically enhanced vimentin expression. At 90°, both enhanced actin and vimentin expression worked cooperatively to maintain cell stability. Specifically, perinuclear actin stress fibers with a large number, low anisotropy, and visible perinuclear vimentin cords were formed onto 2.5 MPa PDMS at 90° for 72 h, supporting the orientation difference in nuclear translocation and global cytoskeleton expression. This orientation dependence tended to disappear onto softer PDMS, presenting distinctive features in nuclear translocation and cytoskeletal structures. Moreover, cellular morphology and focal adhesion were mainly affected by substrate stiffness, yielding a time course of increased spreading area at 24 h but decreased area at 72 h with a decrease of stiffness. Mechanistically, the cell tended to be stabilized onto these PDMS substrates β1 integrin-focal adhesion complexes-actin mechanosensitive axis. These results provided an insight in understanding the combination of substrate stiffness and orientation in defining the mechanical stability of rMSCs.

摘要

源自细胞微环境的不同物理因素对干细胞的生物稳态至关重要。虽然已知底物硬度和取向分别调节间充质干细胞(MSC)的机械重塑和命运决定,但尚不清楚这两个因素如何结合以在重力矢量下操纵其机械稳定性。在这里,我们通过将大鼠MSC置于向上(180°)、向下(0°)或边缘(90°)取向的硬度变化的聚二甲基硅氧烷(PDMS)底物上来量化这些联合效应。与玻璃盖玻片上的值相比,由于细胞核与细胞质之间的密度差异,在2.5MPa PDMS底物上,核纵向易位在0°时24小时较低,在90°时24小时和72小时较高。在0°时,细胞通过显著减少的肌动蛋白和显著增强的波形蛋白表达得到机械支持。在90°时,增强的肌动蛋白和波形蛋白表达协同作用以维持细胞稳定性。具体而言,在90°下72小时,在2.5MPa PDMS上形成了大量、低各向异性且可见核周波形蛋白索的核周肌动蛋白应力纤维,支持了核易位和整体细胞骨架表达的取向差异。这种取向依赖性在较软的PDMS上趋于消失,在核易位和细胞骨架结构上呈现出独特的特征。此外,细胞形态和粘着斑主要受底物硬度影响,在24小时时随着刚度降低,铺展面积增加,但在72小时时面积减小。从机制上讲,细胞倾向于在这些PDMS底物上通过β1整合素-粘着斑复合物-肌动蛋白机械敏感轴实现稳定。这些结果为理解底物硬度和取向在定义大鼠间充质干细胞机械稳定性方面的结合提供了见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4bc6/8859489/c4c3ac05b144/fbioe-09-724101-g001.jpg

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