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Integral role of platelet-derived growth factor in mediating transforming growth factor-β1-dependent mesenchymal stem cell stiffening.血小板衍生生长因子在介导转化生长因子-β1依赖性间充质干细胞硬化中的核心作用。
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Degradation-mediated cellular traction directs stem cell fate in covalently crosslinked three-dimensional hydrogels.降解介导的细胞牵引力指导了共价交联三维水凝胶中的干细胞命运。
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结构和力学线索引导间充质干细胞与交联明胶支架的相互作用。

Architectural and mechanical cues direct mesenchymal stem cell interactions with crosslinked gelatin scaffolds.

作者信息

McAndrews Kathleen M, Kim Min Jeong, Lam Tuyet Y, McGrail Daniel J, Dawson Michelle R

机构信息

1 School of Chemical and Biomolecular Engineering, Georgia Institute of Technology , Atlanta, Georgia .

出版信息

Tissue Eng Part A. 2014 Dec;20(23-24):3252-60. doi: 10.1089/ten.TEA.2013.0753.

DOI:10.1089/ten.TEA.2013.0753
PMID:24873687
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4259178/
Abstract

Naturally derived biomaterials have emerged as modulators of cell function and tissue substitutes. Here, we developed crosslinked glutaraldehyde (GTA) scaffolds for the expansion and differentiation of mesenchymal stem cells (MSCs). The mechanical and architectural properties of the scaffolds were altered by varying the concentration of gelatin and GTA. Higher GTA concentrations were associated with an increase in more confined pores and osteogenic differentiation. In addition, myogenic potential varied with crosslinking degree, although bulk mechanical properties were unaltered. Correlation analysis revealed that ALP activity of differentiated MSCs on higher gelatin concentration scaffolds was dependent on traditional effectors, including environment elasticity and spread area. In contrast, the differentiation capacity of cells cultured on lower gelatin concentration scaffolds did not correlate with these factors, instead it was dependent on the hydrated pore structure. These results suggest that scaffold composition can determine what factors direct differentiation and may have critical implications for biomaterial design.

摘要

天然衍生的生物材料已成为细胞功能的调节剂和组织替代物。在此,我们开发了用于间充质干细胞(MSC)扩增和分化的交联戊二醛(GTA)支架。通过改变明胶和GTA的浓度来改变支架的力学和结构特性。较高的GTA浓度与更狭窄的孔隙增加和成骨分化相关。此外,尽管整体力学性能未改变,但成肌潜力随交联程度而变化。相关分析表明,在较高明胶浓度支架上分化的MSC的碱性磷酸酶(ALP)活性取决于传统效应因子,包括环境弹性和铺展面积。相反,在较低明胶浓度支架上培养的细胞的分化能力与这些因素无关,而是取决于水合孔隙结构。这些结果表明,支架组成可以决定指导分化的因素,并且可能对生物材料设计具有关键意义。