Effects of collagen density on cardiac fibroblast behavior and gene expression

Interactions between cells and the extracellular matrix (ECM) play essential roles in modulating cell behavior during development and disease. The myocardial ECM is composed predominantly of interstitial collagen type I and type III. The composition, organization, and accumulation of these collagens are altered concurrent with cardiovascular development and disease. Changes in these parameters are thought to play significant roles in myocardial function. While a number of studies have examined how changes in the ECM affect myocardial function as a whole, much less is known regarding the response at the cellular level to changes in the collagenous ECM. Experiments were carried out to determine the effects of alterations in collagen density and ECM stiffness on the behavior of isolated heart fibroblasts. In vitro bioassays were performed to measure the effects of changes in collagen concentration (0.75–1.25 mg/ml) on adhesion, migration, spreading, and gene expression by heart fibroblasts. Increased density of collagen in 3‐dimensional gels resulted in more efficient adhesion, spreading, and migration by heart fibroblasts. These experiments indicated that the density of the collagen matrix has a significant impact on fibroblast function. These studies begin to elucidate the effects of ECM density at the cellular level in the myocardium. J. Cell. Physiol. 196: 504–511, 2003. © 2003 Wiley‐Liss, Inc.

[1]  J. Foidart,et al.  Influence of basement membrane molecules on directional migration of human breast cell lines in vitro. , 1991, Journal of cell science.

[2]  M. Eghbali,et al.  Collagen chain mRNAs in isolated heart cells from young and adult rats. , 1988, Journal of molecular and cellular cardiology.

[3]  J. D’Armiento Matrix metalloproteinase disruption of the extracellular matrix and cardiac dysfunction. , 2002, Trends in cardiovascular medicine.

[4]  R. Perris,et al.  Amphibian neural crest cell migration on purified extracellular matrix components: a chondroitin sulfate proteoglycan inhibits locomotion on fibronectin substrates , 1987, The Journal of cell biology.

[5]  T. Borg,et al.  Specific attachment of collagen to cardiac myocytes: in vivo and in vitro. , 1983, Developmental biology.

[6]  S. Factor,et al.  Skeletal framework of mammalian heart muscle. Arrangement of inter- and pericellular connective tissue structures. , 1983, Laboratory investigation; a journal of technical methods and pathology.

[7]  G. G. Reid,et al.  Human leucocyte migration through collagen matrices containing other extracellular matrix components. , 1991, Cell biology international reports.

[8]  T. Borg,et al.  Expression and accumulation of interstitial collagen in the neonatal rat heart , 1993, The Anatomical record.

[9]  T. Borg,et al.  Role of the α1β1 integrin complex in collagen gel contraction in vitro by fibroblasts , 1995 .

[10]  M. Klima,et al.  Morphometry of the aging heart. , 1990, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

[11]  S. Sen,et al.  Changes in collagen phenotypes during progression and regression of cardiac hypertrophy. , 1997, Cardiovascular research.

[12]  S. Sen,et al.  Collagen phenotypes during development and regression of myocardial hypertrophy in spontaneously hypertensive rats. , 1990, Circulation research.

[13]  L. Leinwand,et al.  Localization of types I, III and IV collagen mRNAs in rat heart cells by in situ hybridization. , 1989, Journal of molecular and cellular cardiology.

[14]  T. Borg,et al.  Myofibrillar and cytoskeletal assembly in neonatal rat cardiac myocytes cultured on laminin and collagen , 1991, Cell and Tissue Research.

[15]  T. Borg,et al.  Modulation of cardiac myocyte phenotype in vitro by the composition and orientation of the extracellular matrix , 1994, Journal of cellular physiology.

[16]  T K Borg,et al.  The collagen matrix of the heart. , 1981, Federation proceedings.

[17]  T. Borg,et al.  Expression of metalloproteases by cardiac myocytes and fibroblasts in vitro. , 1997, Cardiovascular pathology : the official journal of the Society for Cardiovascular Pathology.

[18]  T. Borg,et al.  Collagen in the heart. , 1979, Texas reports on biology and medicine.

[19]  D. Newgreen,et al.  Do cells show an inverse locomotory response to fibronectin and laminin substrates? , 1985, The EMBO journal.

[20]  H. Levine,et al.  Mechanical Properties of Rat Cardiac Muscle during Experimental Hypertrophy , 1971, Circulation research.

[21]  T. Borg,et al.  Collagen expression in mechanically stimulated cardiac fibroblasts. , 1991, Circulation research.

[22]  M. Eghbali,et al.  Regulation of fibrillar collagen types I and III and basement membrane type IV collagen gene expression in pressure overloaded rat myocardium. , 1990, Circulation research.

[23]  T. Borg,et al.  The Role of the Extracellular Matrix and Its Receptors in Modulating Cardiac Development , 2001 .

[24]  J. S. Janicki,et al.  Myocardial collagen remodeling in pressure overload hypertrophy. A case for interstitial heart disease. , 1989, American journal of hypertension.

[25]  P. Whittaker Collagen organization in wound healing after myocardial injury , 1998, Basic Research in Cardiology.

[26]  L. B. Mesiano Maifrino,et al.  Age related changes of the collagen network of the human heart. , 2001, Mechanisms of ageing and development.

[27]  M. Zile,et al.  Collagen remodeling and changes in LV function during development and recovery from supraventricular tachycardia. , 1991, The American journal of physiology.

[28]  T. Borg,et al.  Interaction of the extracellular matrix with cardiac myocytes during development and disease , 1990 .

[29]  J W Covell,et al.  Structural and mechanical factors influencing infarct scar collagen organization. , 2000, American journal of physiology. Heart and circulatory physiology.

[30]  M. Dembo,et al.  Cell movement is guided by the rigidity of the substrate. , 2000, Biophysical journal.

[31]  W. Carver,et al.  Angiotensin II‐stimulated collagen gel contraction by heart fibroblasts: Role of the AT1 receptor and tyrosine kinase activity , 1998, Journal of cellular physiology.

[32]  S. Shroff,et al.  Fibrillar Collagen and Myocardial Stiffness in the Intact Hypertrophied Rat Left Ventricle , 1989, Circulation research.

[33]  S. Shroff,et al.  Physiologic Versus Pathologic Hypertrophy and the Pressure‐Overloaded Myocardium , 1987, Journal of cardiovascular pharmacology.