Surface Roughness Gradients Reveal Topography-Specific Mechanosensitive Responses in Human Mesenchymal Stem Cells

被引:202
作者
Hou, Yong [1 ]
Xie, Wenyan [2 ]
Yu, Leixiao [1 ]
Camacho, Luis Cuellar [1 ]
Nie, Chuanxiong [1 ]
Zhang, Man [3 ]
Haag, Rainer [1 ]
Wei, Qiang [3 ]
机构
[1] Free Univ Berlin, Inst Chem & Biochem, Takustr 3, D-14195 Berlin, Germany
[2] Free Univ Berlin, Inst Pharm, Konigin Luise Str 2 4, D-14195 Berlin, Germany
[3] Sichuan Univ, Coll Polymer Sci & Engn, State Key Lab Polymer Mat & Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
cell adhesion; cell differentiation; mechanotransduction; mesenchymal stem cells; roughness gradient; LAMIN-A; DIFFERENTIATION; ADHESION; YAP/TAZ; NANO; MECHANOTRANSDUCTION; NANOTOPOGRAPHY; CHEMISTRY; COATINGS; GROWTH;
D O I
10.1002/smll.201905422
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The topographic features of an implant, which mechanically regulate cell behaviors and functions, are critical for the clinical success in tissue regeneration. How cells sense and respond to the topographical cues, e.g., interfacial roughness, is yet to be fully understood and even debatable. Here, the mechanotransduction and fate determination of human mesenchymal stem cells (MSCs) on surface roughness gradients are systematically studied. The broad range of topographical scales and high-throughput imaging is achieved based on a catecholic polyglycerol coating fabricated by a one-step-tilted dip-coating approach. It is revealed that the adhesion of MSCs is biphasically regulated by interfacial roughness. The cell mechanotransduction is investigated from focal adhesion to transcriptional activity, which explains that cellular response to interfacial roughness undergoes a direct force-dependent mechanism. Moreover, the optimized roughness for promoting cell fate specification is explored.
引用
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页数:10
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