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自增强黏附力促进细胞力学转导。

Self-Strengthening Adhesive Force Promotes Cell Mechanotransduction.

机构信息

Institute of Chemistry and Biochemistry, Freie Universität Berlin, Takustr. 3, Berlin, 14195, Germany.

Institute of Pharmacy, Freie Universität Berlin, Königin-Luise-Str. 2+4, Berlin, 14195, Germany.

出版信息

Adv Mater. 2020 Dec;32(52):e2006986. doi: 10.1002/adma.202006986. Epub 2020 Nov 18.


DOI:10.1002/adma.202006986
PMID:33206452
Abstract

The extracellular matrix (ECM) undergoes dynamic remodeling and progressive stiffening during tissue regeneration and disease progression. However, most of the artificial ECMs and in vitro disease models are mechanically static. Here, a self-strengthening polymer coating mimicking the dynamic nature of native ECM is designed to study the cellular response to dynamic biophysical cues and promote cell mechanical sensitive response. Spiropyran (SP) is utilized as dynamic anchor group to regulate the strength of cell adhesive peptide ligands. Benefiting from spontaneous thermal merocyanine-to-spiropyran (MC-SP) isomerization, the resulting self-responsive coating displays dynamic self-strengthening of interfacial interactions. Comparing with the static and all of the previous dynamic artificial ECMs, cells on this self-responsive surface remodel the weakly bonded MC-based coatings to activate α5β1 integrin and Rac signaling in the early adhesion stage. The subsequent MC-to-SP conversion strengthens the ligand-integrin interaction to further activate αvβ3 integrin and RhoA/ROCK signaling in the latter stage. This sequential process enhances cellular mechanotransduction as well as the osteogenic differentiation of mesenchymal stem cells (MSCs). It is worth emphasizing that the self-strengthening occurs spontaneously in the absence of any stimulus, making it especially useful for implanted scaffolds in regenerative medicine.

摘要

细胞外基质 (ECM) 在组织再生和疾病进展过程中经历动态重塑和渐进性变硬。然而,大多数人工 ECM 和体外疾病模型在力学上是静态的。在这里,设计了一种模仿天然 ECM 动态特性的自增强聚合物涂层,以研究细胞对动态生物物理线索的反应并促进细胞机械敏感反应。螺吡喃 (SP) 被用作动态锚定基团来调节细胞黏附肽配体的强度。得益于自发的热分子内酰基迁移(MC-SP)异构化,所得自响应涂层表现出界面相互作用的动态自增强。与静态和之前所有的动态人工 ECM 相比,在早期黏附阶段,细胞会重塑弱键合的基于 MC 的涂层以激活α5β1 整合素和 Rac 信号通路。随后的 MC 到 SP 的转化加强了配体-整合素的相互作用,以在后期进一步激活αvβ3 整合素和 RhoA/ROCK 信号通路。这个连续的过程增强了细胞的力学转导以及间充质干细胞 (MSCs) 的成骨分化。值得强调的是,自增强是在没有任何刺激的情况下自发发生的,这使其特别适用于再生医学中的植入支架。

相似文献

[1]
Self-Strengthening Adhesive Force Promotes Cell Mechanotransduction.

Adv Mater. 2020-12

[2]
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[3]
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[4]
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[5]
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[6]
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[7]
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[8]
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[9]
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J Biol Chem. 2015-3-13

[10]
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[9]
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