Geometric constraint of mechanosensing by modification of hydrogel thickness prevents stiffness-induced differentiation in bone marrow stromal cells.

IF 3.7 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Journal of The Royal Society Interface Pub Date : 2024-10-01 Epub Date: 2024-10-02 DOI:10.1098/rsif.2024.0485
Maria L Hernandez-Miranda, Dichu Xu, Aya A Ben Issa, David A Johnston, Martin Browne, Richard B Cook, Bram G Sengers, Nicholas Evans
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引用次数: 0

Abstract

Extracellular matrix (ECM) stiffness is fundamental in cell division, movement and differentiation. The stiffness that cells sense is determined not only by the elastic modulus of the ECM material but also by ECM geometry and cell density. We hypothesized that these factors would influence cell traction-induced matrix deformations and cellular differentiation in bone marrow stromal cells (BMSCs). To achieve this, we cultivated BMSCs on polyacrylamide hydrogels that varied in elastic modulus and geometry and measured cell spreading, cell-imparted matrix deformations and differentiation. At low cell density BMSCs spread to a greater extent on stiff compared with soft hydrogels, or on thin compared with thick hydrogels. Cell-imparted matrix deformations were greater on soft compared with stiff hydrogels or thick compared with thin hydrogels. There were no significant differences in osteogenic differentiation relative to hydrogel elastic modulus and thickness. However, increased cell density and/or prolonged culture significantly reduced matrix deformations on soft hydrogels to levels similar to those on stiff substrates. This suggests that at high cell densities cell traction-induced matrix displacements are reduced by both neighbouring cells and the constraint imposed by an underlying stiff support. This may explain observations of the lack of difference in osteogenic differentiation as a function of stiffness.

通过改变水凝胶厚度对机械传感进行几何限制,可防止骨髓基质细胞因僵化而分化。
细胞外基质(ECM)的硬度是细胞分裂、运动和分化的基础。细胞感受到的硬度不仅取决于 ECM 材料的弹性模量,还取决于 ECM 的几何形状和细胞密度。我们假设这些因素会影响细胞牵引引起的基质变形和骨髓基质细胞(BMSCs)的细胞分化。为此,我们在不同弹性模量和几何形状的聚丙烯酰胺水凝胶上培养骨髓基质干细胞,并测量了细胞铺展、细胞引起的基质变形和分化。在低细胞密度下,BMSC 在硬水凝胶上的扩散程度比在软水凝胶上的扩散程度大,或在薄水凝胶上的扩散程度比在厚水凝胶上的扩散程度大。软水凝胶与硬水凝胶相比,或厚水凝胶与薄水凝胶相比,细胞诱导的基质变形更大。相对于水凝胶的弹性模量和厚度,成骨分化没有明显差异。然而,细胞密度的增加和/或培养时间的延长会显著降低软水凝胶上基质的变形,使其与硬基质上的变形水平相似。这表明,在高细胞密度下,细胞牵引引起的基质位移会因邻近细胞和底层坚硬支撑物的限制而减小。这也许可以解释为什么观察到的成骨分化与硬度的函数关系没有差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of The Royal Society Interface
Journal of The Royal Society Interface 综合性期刊-综合性期刊
CiteScore
7.10
自引率
2.60%
发文量
234
审稿时长
2.5 months
期刊介绍: J. R. Soc. Interface welcomes articles of high quality research at the interface of the physical and life sciences. It provides a high-quality forum to publish rapidly and interact across this boundary in two main ways: J. R. Soc. Interface publishes research applying chemistry, engineering, materials science, mathematics and physics to the biological and medical sciences; it also highlights discoveries in the life sciences of relevance to the physical sciences. Both sides of the interface are considered equally and it is one of the only journals to cover this exciting new territory. J. R. Soc. Interface welcomes contributions on a diverse range of topics, including but not limited to; biocomplexity, bioengineering, bioinformatics, biomaterials, biomechanics, bionanoscience, biophysics, chemical biology, computer science (as applied to the life sciences), medical physics, synthetic biology, systems biology, theoretical biology and tissue engineering.
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