The effect of growth factor environment on fibroblast morphological response to substrate stiffness

被引:32
作者
Grinnell, Frederick [1 ]
Ho, Chin-Han [1 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Cell Biol, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
Cell spreading; Collagen; Compliance; Fibronectin; Growth factors; Mechanical properties; EXTRACELLULAR-MATRIX; CELL MOTILITY; COLLAGEN; MIGRATION; DIFFERENTIATION; ADHESIONS; ACTIN; MECHANICS; SCAFFOLDS; DYNAMICS;
D O I
10.1016/j.biomaterials.2012.10.036
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
According to conventional understanding regarding dependence of cell behavior on substrate stiffness, tissue cells typically remain round on soft substrates but spread on stiff substrates. The current studies were carried out to learn if the growth factor environment influenced the foregoing relationship. Using standard methods, we prepared planar (2D) polyacrylamide (PA) gels ranging from 0.5 to 40 kPa and covalently cross-linked with fibronectin and collagen at concentrations ranging from 2.5 to 50 mu g/ml. We carried out experiments with fibroblasts varying in their ability to form actin stress fibers and focal adhesions. In fetal bovine serum (FBS) containing medium - the growth factor environment in which most studies on cell spreading and substrate stiffness have been carried out - cell spreading increased with increasing substrate stiffness and adhesion ligand density. However, in platelet-derived growth factor (PDGF) containing medium, cell spreading was relatively independent of substrate stiffness and adhesion ligand density except little cell attachment occurred in the complete absence of cross-linked adhesion ligands. If cell contraction was blocked with blebbistatin, then cell spreading in FBS-containing medium became independent of substrate stiffness. The findings suggest that under growth factor conditions that stimulate global cell contraction (FBS), cell spreading cannot occur unless adhesion ligand density and substrate stiffness result in cell-substrate interactions strong enough to resist and overcome the inward tractional force. Under growth factor conditions that stimulate global cell protrusion (PDGF), such resistance is not required. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:965 / 974
页数:10
相关论文
共 41 条
[21]   Vascular Smooth Muscle Cell Durotaxis Depends on Substrate Stiffness Gradient Strength [J].
Isenberg, Brett C. ;
DiMilla, Paul A. ;
Walker, Matthew ;
Kim, Sooyoung ;
Wong, Joyce Y. .
BIOPHYSICAL JOURNAL, 2009, 97 (05) :1313-1322
[22]   Growth Factor Regulation of Corneal Keratocyte Differentiation and Migration in Compressed Collagen Matrices [J].
Kim, Areum ;
Lakshman, Neema ;
Karamichos, Dimitris ;
Petroll, W. Matthew .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2010, 51 (02) :864-875
[23]   Mechanosensing Can Result from Adhesion Molecule Dynamics [J].
Krzyszczyk, Paulina ;
Wolgemuth, Charles W. .
BIOPHYSICAL JOURNAL, 2011, 101 (10) :L53-L55
[24]   Cell movement is guided by the rigidity of the substrate [J].
Lo, CM ;
Wang, HB ;
Dembo, M ;
Wang, YL .
BIOPHYSICAL JOURNAL, 2000, 79 (01) :144-152
[25]   The extracellular matrix: A dynamic niche in cancer progression [J].
Lu, Pengfei ;
Weaver, Valerie M. ;
Werb, Zena .
JOURNAL OF CELL BIOLOGY, 2012, 196 (04) :395-406
[26]   Synthetic biomaterials as instructive extracellular microenvironments for morphogenesis in tissue engineering [J].
Lutolf, MP ;
Hubbell, JA .
NATURE BIOTECHNOLOGY, 2005, 23 (01) :47-55
[27]   Oncogenic Ras-transformed human fibroblasts exhibit differential changes in contraction and migration in 3D collagen matrices [J].
Menezes, Gustavo C. ;
Miron-Mendoza, Miguel ;
Ho, Chin-Han ;
Jiang, Hongmei ;
Grinnell, Frederick .
EXPERIMENTAL CELL RESEARCH, 2008, 314 (16) :3081-3091
[28]   The differential regulation of cell motile activity through matrix stiffness and porosity in three dimensional collagen matrices [J].
Miron-Mendoza, Miguel ;
Seemann, Joachim ;
Grinnell, Frederick .
BIOMATERIALS, 2010, 31 (25) :6425-6435
[29]   Of extracellular matrix, scaffolds, and signaling: Tissue architecture regulates development, homeostasis, and cancer [J].
Nelson, Celeste M. ;
Bissell, Mina J. .
ANNUAL REVIEW OF CELL AND DEVELOPMENTAL BIOLOGY, 2006, 22 :287-309
[30]   Mechanobiology of scarring [J].
Ogawa, Rei .
WOUND REPAIR AND REGENERATION, 2011, 19 :S2-S9