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Effect of Polyelectrolyte Film Stiffness on Endothelial Cells During Endothelial-to-Mesenchymal Transition.
Zhang, He; Chang, Hao; Wang, Li-mei; Ren, Ke-feng; Martins, M Cristina L; Barbosa, Mário A; Ji, Jian.
Afiliação
  • Zhang H; MOE Key Laboratory of Macromolecule Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University , Hangzhou 310027, China.
  • Chang H; MOE Key Laboratory of Macromolecule Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University , Hangzhou 310027, China.
  • Wang LM; MOE Key Laboratory of Macromolecule Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University , Hangzhou 310027, China.
  • Ren KF; MOE Key Laboratory of Macromolecule Synthesis and Functionalization, Department of Polymer Science and Engineering, Zhejiang University , Hangzhou 310027, China.
  • Martins MC; State Key Laboratory of Molecular Engineering of Polymers, Fudan University , Shanghai, China.
  • Barbosa MA; INEB - Instituto de Engenharia Biomédica, Universidade do Porto , Rua do Campo Alegre, 823, 4150-180, Porto, Portugal.
  • Ji J; INEB - Instituto de Engenharia Biomédica, Universidade do Porto , Rua do Campo Alegre, 823, 4150-180, Porto, Portugal.
Biomacromolecules ; 16(11): 3584-93, 2015 Nov 09.
Article em En | MEDLINE | ID: mdl-26477358
ABSTRACT
Endothelial-to-mesenchymal transition (EndMT), during which endothelial cells (ECs) transdifferentiate into mesenchymal phenotype, plays a key role in the development of vascular implant complications such as endothelium dysfunction and in-stent restenosis. Substrate stiffness has been confirmed as a key factor to influence EC behaviors; however, so far, the relationship between substrate stiffness and EndMT has been rarely studied. Here, ECs were cultured on the (poly(L-lysine)/hyaluronate acid) (PLL/HA) multilayer films with controlled stiffness for 2 weeks, and their EndMT behaviors were studied. We demonstrated that ECs lost their markers (vWf and CD31) in a stiffness-dependent manner even without supplement of growth factors, and the softer film favored the maintaining of EC phenotype. Further, induced by transforming growth factor ß1 (TGF-ß1), ECs underwent EndMT, as characterized by losing their typical cobblestone morphology and markers and gaining smooth muscle cell markers (α-smooth muscle actin and calponin). Interestingly, stronger EndMT was observed when ECs were cultured on the stiffer film. Collectively, our findings suggest that substrate stiffness has significant effects on EndMT, and a softer substrate is beneficial to ECs by keeping their phenotype and inhibiting EndMT, which presents a new strategy for surface design of vascular implant materials.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transdiferenciação Celular / Transição Epitelial-Mesenquimal / Células Endoteliais da Veia Umbilical Humana Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transdiferenciação Celular / Transição Epitelial-Mesenquimal / Células Endoteliais da Veia Umbilical Humana Limite: Humans Idioma: En Ano de publicação: 2015 Tipo de documento: Article