The effects of matrix stiffness and RhoA on the phenotypic plasticity of smooth muscle cells in a 3-D biosynthetic hydrogel system

被引:175
作者
Peyton, Shelly R. [2 ]
Kim, Peter D. [1 ]
Ghajar, Cyrus M. [1 ]
Seliktar, Dror [3 ]
Putnam, Andrew J. [1 ,2 ]
机构
[1] Univ Calif Irvine, Dept Biomed Engn, Henry Samueli Sch Engn, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Dept Chem Engn & Mat Sci, Henry Samueli Sch Engn, Irvine, CA 92697 USA
[3] Technion Israel Inst Technol, Fac Biomed Engn, IL-32000 Haifa, Israel
关键词
ECM (extracellular matrix); hydrogel; mechanical properties; polyethylene oxide; smooth muscle cell;
D O I
10.1016/j.biomaterials.2008.02.005
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Studies using 2-D cultures have shown that the mechanical properties of the extracellular matrix (ECM) influence cell migration, spreading, proliferation, and differentiation; however, cellular mechanosensing in 3-D remains under-explored. To investigate this topic, a unique biomaterial system based on poly(ethylene glycol)-conjugated fibrinogen was adapted to study phenotypic plasticity in smooth muscle cells (SMCs) as a function of ECM mechanics in 3-D. Tuning the compressive modulus between 448 and 5804 Pa modestly regulated SMC cytoskeletal assembly in 3-D3, with spread cells in stiff matrices having a slightly higher degree of F-actin bundling after prolonged culture. However, vinculin expression in all 3-D conditions was qualitatively low and was not assembled into the classic focal adhesions typically seen in 2-D cultures. Given the evidence that RhoA-mediated cytoskeletal contractility represents a critical node in mechanosensing, we molecularly upregulated contractility by inducing SMCs to express constitutively active RhoA. In these cells, F-actin bundling and total vinculin expression increased, and focal adhesion-like structures began to emerge, consistent with RhoA' mechanism of action in cells cultured on 2-D substrates. Furthermore, SMC proliferation in 3-D did not depend significantly on matrix stiffness, and was reduced by constitutive activation of RhoA irrespective of ECM mechanical properties. Conversely, the expression of contractile markers globally increased with constitutive RhoA activation and depended on 3-D matrix stiffness only in cells with heightened RhoA activity. Combined, these data suggest that the synergistic effects of ECM mechanics and RhoA activity on SMC phenotype in 3-D are distinct from those in 2-D, and highlight the importance of studying the mechanical role of cell-matrix interactions in tunable 3-D environments. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2597 / 2607
页数:11
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