Fibroblast growth factor-2 decreases metabolic coupling and stimulates phosphorylation as well as masking of connexin43 epitopes in cardiac myocytes.

Cardiac gap junction (GJ) channels, composed of connexins, allow electrical and metabolic couplings between cardiomyocytes, properties important for coordinated action of the heart as well as tissue homeostasis and control of growth and differentiation. Fibroblast growth factor-2 (FGF-2) is an endogenous growth-promoting protein, believed to participate in the short- and long-term responses of the heart to injury. We have examined short-term effects of FGF-2 on cardiac myocyte GJ-mediated metabolic coupling, using cultures of neonatal rat cardiomyocytes. FGF-2 decreased coupling between cardiomyocytes assessed by scrape dye loading as well as microinjection and dye transfer within 30 minutes of administration. Genistein blocked the effects of FGF-2. To determine the mechanism, we next assessed the effect of FGF-2 on expression, distribution, and phosphorylation of connexin43 (Cx43), which is a major cardiomyocyte connexin. FGF-2 did not affect Cx43 mRNA or protein accumulation and synthesis, and it did not change Cx43 localization at sites of intercellular contact as assessed by immunostaining with a polyclonal anti-Cx43 antibody raised against a synthetic peptide containing residues 346 to 363 of Cx43. FGF-2, however, decreased staining intensity at sites of intermyocyte contact when a monoclonal anti-Cx43 antibody was used, suggesting a localized masking of epitope(s) recognized by the monoclonal but not the polyclonal antibody. These epitopes appear to reside within residues 261 to 270 of Cx43, as indicated by full quenching of monoclonal antibody staining with synthetic peptides. In addition, FGF-2 induced a more than twofold increase in Cx43 phosphorylation. Phosphoamino acid analysis indicated increased phosphorylation of Cx43 on serine residues. Although tyrosine phosphorylation of Cx43 was not detected in either treated or control cells, a fraction of Cx43 was immunoprecipitated with anti-phosphotyrosine-specific antibodies in FGF-2-treated myocytes, suggesting interaction (and hence coprecipitation) with phosphotyrosine-containing protein(s). In conclusion, we have identified Cx43 and intercellular communication as targets of FGF-2-triggered and tyrosine phosphorylation-dependent signal transduction in cardiac myocytes. It is suggested that phosphorylation of Cx43 on serine induced by FGF-2 contributes to decreased metabolic coupling between cardiomyocytes.

[1]  P. Lampe,et al.  Characterization of the Mitogen-activated Protein Kinase Phosphorylation Sites on the Connexin-43 Gap Junction Protein (*) , 1996, The Journal of Biological Chemistry.

[2]  D. Kaye,et al.  Role of transiently altered sarcolemmal membrane permeability and basic fibroblast growth factor release in the hypertrophic response of adult rat ventricular myocytes to increased mechanical activity in vitro. , 1996, The Journal of clinical investigation.

[3]  E. Kardami,et al.  Cardioprotection and Basic Fibroblast Growth Factor , 1996 .

[4]  E. Kardami,et al.  High and low molecular weight fibroblast growth factor-2 increase proliferation of neonatal rat cardiac myocytes but have differential effects on binucleation and nuclear morphology. Evidence for both paracrine and intracrine actions of fibroblast growth factor-2. , 1996, Circulation research.

[5]  P. Brink,et al.  Selectivity of connexin-specific gap junctions does not correlate with channel conductance. , 1995, Circulation research.

[6]  H. Jongsma,et al.  TPA increases conductance but decreases permeability in neonatal rat cardiomyocyte gap junction channels. , 1995, Experimental cell research.

[7]  J. Feige,et al.  Basic Fibroblast Growth Factor Activates Calcium Channels in Neonatal Rat Cardiomyocytes (*) , 1995, The Journal of Biological Chemistry.

[8]  H. Chiao,et al.  Contraction-induced cell wounding and release of fibroblast growth factor in heart. , 1995, Circulation research.

[9]  C. Zuppan,et al.  Mutations of the Connexin43 gap-junction gene in patients with heart malformations and defects of laterality. , 1995, The New England journal of medicine.

[10]  K. Willecke,et al.  Specific permeability and selective formation of gap junction channels in connexin-transfected HeLa cells , 1995, The Journal of cell biology.

[11]  B L Langille,et al.  Cardiac malformation in neonatal mice lacking connexin43. , 1995, Science.

[12]  J. Saffitz,et al.  Expression of multiple connexins in cultured neonatal rat ventricular myocytes. , 1995, Circulation research.

[13]  B. Doble,et al.  Regulation of Basic Fibroblast Growth Factor (BFGF) and FGF Receptors in the Heart a , 1995, Annals of the New York Academy of Sciences.

[14]  N. Dhalla,et al.  Heart Hypertrophy and Failure , 1995, Developments in Cardiovascular Medicine.

[15]  N. Dekel,et al.  Phosphorylation and expression of connexin-43 ovarian gap junction protein are regulated by luteinizing hormone. , 1994, The Journal of biological chemistry.

[16]  A. Moreno,et al.  Human connexin43 gap junction channels. Regulation of unitary conductances by phosphorylation. , 1994, Circulation research.

[17]  K. Willecke,et al.  Immunochemical and electrophysiological characterization of murine connexin40 and -43 in mouse tissues and transfected human cells. , 1994, European journal of cell biology.

[18]  P. Parker,et al.  Endothelin-1 and fibroblast growth factors stimulate the mitogen-activated protein kinase signaling cascade in cardiac myocytes. The potential role of the cascade in the integration of two signaling pathways leading to myocyte hypertrophy. , 1994, The Journal of biological chemistry.

[19]  A. Lau,et al.  Epidermal growth factor stimulates the disruption of gap junctional communication and connexin43 phosphorylation independent of 12-0-tetradecanoylphorbol 13-acetate-sensitive protein kinase C: the possible involvement of mitogen-activated protein kinase. , 1993, Molecular biology of the cell.

[20]  B. Doble,et al.  Basic fibroblast growth factor in cardiac myocytes: expression and effects , 1993 .

[21]  E. Kardami,et al.  Increased basic fibroblast growth factor (bFGF) accumulation and distinct patterns of localization in isoproterenol-induced cardiomyocyte injury. , 1993, Growth factors.

[22]  A. Moreno,et al.  Gap junctions. Multiplicity of controls in differentiated and undifferentiated cells and possible functional implications. , 1993, Advances in second messenger and phosphoprotein research.

[23]  P. Cummins Growth Factors and the Cardiovascular System , 1993, Developments in Cardiovascular Medicine.

[24]  P. Meda,et al.  Basic fibroblast growth factor increases junctional communication and connexin 43 expression in microvascular endothelial cells , 1992, Journal of cellular physiology.

[25]  A. Boynton,et al.  Epidermal growth factor disrupts gap-junctional communication and induces phosphorylation of connexin43 on serine. , 1992, Molecular biology of the cell.

[26]  K. Chien,et al.  Microinjection of Antibodies and Expression Vectors Into Living Myocardial Cells: Development of a Novel Approach to Identify Candidate Genes That Regulate Cardiac Growth and Hypertrophy , 1992, Circulation.

[27]  J. Saffitz,et al.  Cardiac myocyte interconnections at gap junctions Role in normal and abnormal electrical conduction. , 1992, Trends in cardiovascular medicine.

[28]  W. Loewenstein,et al.  The cell-cell channel in the control of growth. , 1992, Seminars in cell biology.

[29]  E. Hertzberg,et al.  Connexin43 in MDCK cells: regulation by a tumor-promoting phorbol ester and Ca2+. , 1992, European journal of cell biology.

[30]  D. Moscatelli,et al.  The FGF family of growth factors and oncogenes. , 1992, Advances in cancer research.

[31]  B. Doble,et al.  Basic Fibroblast Growth Factor in Cultured Cardiac Myocytes a , 1991, Annals of the New York Academy of Sciences.

[32]  D. Goodenough,et al.  Biochemical analysis of connexin43 intracellular transport, phosphorylation, and assembly into gap junctional plaques , 1991, The Journal of cell biology.

[33]  E. Kardami,et al.  Distinctive patterns of basic fibroblast growth factor (bFGF) distribution in degenerating and regenerating areas of dystrophic (mdx) striated muscles. , 1991, Developmental biology.

[34]  E. Krebs,et al.  Consensus sequences as substrate specificity determinants for protein kinases and protein phosphatases. , 1991, The Journal of biological chemistry.

[35]  E. Krebs,et al.  Phosphorylation of neuromodulin (GAP-43) by casein kinase II. Identification of phosphorylation sites and regulation by calmodulin. , 1991, The Journal of biological chemistry.

[36]  D. S. Crow,et al.  Evidence that heart connexin43 is a phosphoprotein. , 1991, Journal of molecular and cellular cardiology.

[37]  J E Saffitz,et al.  Remodeling of ventricular conduction pathways in healed canine infarct border zones. , 1991, The Journal of clinical investigation.

[38]  E. Krebs,et al.  Multiple components in an epidermal growth factor-stimulated protein kinase cascade. In vitro activation of a myelin basic protein/microtubule-associated protein 2 kinase. , 1991, The Journal of biological chemistry.

[39]  E. Hertzberg,et al.  Gap junctions: New tools, new answers, new questions , 1991, Neuron.

[40]  C. Naus,et al.  Transfection of C6 glioma cells with connexin 43 cDNA: analysis of expression, intercellular coupling, and cell proliferation. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[41]  T. Hunter,et al.  Phosphopeptide mapping and phosphoamino acid analysis by two-dimensional separation on thin-layer cellulose plates. , 1991, Methods in enzymology.

[42]  T. Parker,et al.  Growth factors, proto-oncogenes, and plasticity of the cardiac phenotype. , 1991, Annual review of physiology.

[43]  H. Piwnica-Worms,et al.  Tyrosine phosphorylation of the gap junction protein connexin43 is required for the pp60v-src-induced inhibition of communication. , 1990, Cell regulation.

[44]  D. S. Crow,et al.  Phosphorylation of connexin43 gap junction protein in uninfected and Rous sarcoma virus-transformed mammalian fibroblasts , 1990, Molecular and cellular biology.

[45]  E. Hertzberg,et al.  LM and EM immunolocalization of the gap junctional protein connexin 43 in rat brain , 1990, Brain Research.

[46]  R. Fandrich,et al.  Basic fibroblast growth factor in atria and ventricles of the vertebrate heart , 1989, The Journal of cell biology.

[47]  R. Lal,et al.  The 43-kD polypeptide of heart gap junctions: immunolocalization, topology, and functional domains , 1989, The Journal of cell biology.

[48]  R. Roberts,et al.  Differentiation of cardiac myocytes after mitogen withdrawal exhibits three sequential states of the ventricular growth response , 1988, The Journal of cell biology.

[49]  D. Paul,et al.  Connexin43: a protein from rat heart homologous to a gap junction protein from liver , 1987, The Journal of cell biology.

[50]  P. Chomczyński,et al.  Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. , 1987, Analytical biochemistry.

[51]  J. Trosko,et al.  Scrape-loading and dye transfer. A rapid and simple technique to study gap junctional intercellular communication. , 1987, Experimental cell research.

[52]  W. Loewenstein The Cell-to-Cell Membrane Channel , 1986 .

[53]  U. K. Laemmli,et al.  Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4 , 1970, Nature.