Mast cell tryptase is a mitogen for cultured fibroblasts.

Mast cells appear to promote fibroblast proliferation, presumably through secretion of growth factors, although the molecular mechanisms underlying this mitogenic potential have not been explained fully by known mast cell-derived mediators. We report here that tryptase, a trypsin-like serine proteinase of mast cell secretory granules, is a potent mitogen for fibroblasts in vitro. Nanomolar concentrations of dog tryptase strongly stimulate thymidine incorporation in Chinese hamster lung and Rat-1 fibroblasts and increase cell density in both subconfluent and confluent cultures of these cell lines. Tryptase-induced cell proliferation appears proteinase-specific, as this response is not mimicked by pancreatic trypsin or mast cell chymase. In addition, low levels of tryptase markedly potentiate DNA synthesis stimulated by epidermal growth factor, basic fibroblast growth factor, or insulin. Inhibitors of catalytic activity decrease the mitogenic capacity of tryptase, suggesting, though not proving, the participation of the catalytic site in cell activation by tryptase. Differences in Ca++ mobilization and sensitivity to pertussis toxin suggest that tryptase and thrombin activate distinct signal transduction pathways in fibroblasts. These data implicate mast cell tryptase as a potent, previously unrecognized fibroblast growth factor, and may provide a molecular link between mast cell activation and fibrosis.

[1]  D. Templeton Proteoglycans in cell regulation. , 1992, Critical reviews in clinical laboratory sciences.

[2]  M. Benezra,et al.  Thrombin immobilized to extracellular matrix is a potent mitogen for vascular smooth muscle cells: nonenzymatic mode of action. , 1990, Cell regulation.

[3]  L. Schwartz,et al.  Interactions of human mast cell tryptase with biological protease inhibitors. , 1990, Archives of biochemistry and biophysics.

[4]  K. Ohta,et al.  Mast cells are important in the development of hypersensitivity pneumonitis. A study with mast-cell-deficient mice. , 1989, Journal of immunology.

[5]  H. Claman On scleroderma. Mast cells, endothelial cells, and fibroblasts. , 1989, JAMA.

[6]  R. Silver,et al.  A STRATEGY FOR DETERMINING THE PATHOGENESIS OF SYSTEMIC SCLEROSIS: Is Transforming Growth Factor β the Answer? , 1989, Arthritis and rheumatism.

[7]  J. Padawer,et al.  Structural Alterations in Fibroblast Monolayers Caused by Mast Cell Degranulation , 1989, Journal of leukocyte biology.

[8]  S. Holgate,et al.  Cellular events in the bronchi in mild asthma and after bronchial provocation. , 1989, The American review of respiratory disease.

[9]  J. Pouysségur,et al.  Signal transduction in hamster fibroblasts overexpressing the human EGF receptor. , 1989, Growth factors.

[10]  J. Nadel,et al.  Mast cell tryptase causes airway smooth muscle hyperresponsiveness in dogs. , 1989, The Journal of clinical investigation.

[11]  J. Fareed,et al.  Thrombin inhibition with dipeptidyl argininals. , 1988, Thrombosis research.

[12]  J. Nadel,et al.  Tryptase and chymase: comparison of extraction and release in two dog mastocytoma lines. , 1988, Immunology.

[13]  J. Nadel,et al.  Purification and characterization of dog mastocytoma chymase: identification of an octapeptide conserved in chymotryptic leukocyte proteinases. , 1988, Biochimica et Biophysica Acta.

[14]  J. Nadel,et al.  Dog mastocytoma tryptase: affinity purification, characterization, and amino-terminal sequence. , 1987, Archives of biochemistry and biophysics.

[15]  M. Ui,et al.  Possible involvement of a GTP-binding protein, the substrate of islet-activating protein, in receptor-mediated signaling responsible for cell proliferation. , 1987, The Journal of biological chemistry.

[16]  J. Meldolesi,et al.  EGF raises cytosolic Ca2+ in A431 and Swiss 3T3 cells by a dual mechanism. Redistribution from intracellular stores and stimulated influx. , 1987, Experimental cell research.

[17]  J. Pouysségur,et al.  Two growth factor signalling pathways in fibroblasts distinguished by pertussis toxin , 1987, Nature.

[18]  L. Schwartz,et al.  Quantitation of histamine, tryptase, and chymase in dispersed human T and TC mast cells. , 1987, Journal of immunology.

[19]  L. Schwartz,et al.  Mediators of human mast cells and human mast cell subsets. , 1987, Annals of allergy.

[20]  W. Scher The role of extracellular proteases in cell proliferation and differentiation. , 1987, Laboratory investigation; a journal of technical methods and pathology.

[21]  J. Pouysségur,et al.  The mitogenic signaling pathway of fibroblast growth factor is not mediated through polyphosphoinositide hydrolysis and protein kinase C activation in hamster fibroblasts. , 1986, The Journal of biological chemistry.

[22]  E. Rozengurt Early signals in the mitogenic response. , 1986, Science.

[23]  R. Penny,et al.  Mast cell granules cause proliferation of human microvascular endothelial cells. , 1986, Laboratory investigation; a journal of technical methods and pathology.

[24]  R. Lavker,et al.  Identification of a chymotrypsin-like proteinase in human mast cells. , 1986, Journal of immunology.

[25]  L. Schwartz,et al.  Regulation of tryptase from human lung mast cells by heparin. Stabilization of the active tetramer. , 1986, The Journal of biological chemistry.

[26]  K. Mann,et al.  Identification of a thrombin sequence with growth factor activity on macrophages. , 1986, Proceedings of the National Academy of Sciences of the United States of America.

[27]  W. Moolenaar Effects of growth factors on intracellular pH regulation. , 1986, Annual review of physiology.

[28]  D. Raben,et al.  Effects of EGF and thrombin on inositol‐containing phospholipids of cultured fibroblasts: Stimulation of phosphatidylinositol synthesis by thrombin but not EGF , 1985, Journal of cellular physiology.

[29]  R. Tsien,et al.  A new generation of Ca2+ indicators with greatly improved fluorescence properties. , 1985, The Journal of biological chemistry.

[30]  J. Bienenstock,et al.  Mast cell heterogeneity and hyperplasia in bleomycin-induced pulmonary fibrosis of rats. , 1984, The American review of respiratory disease.

[31]  D. Johnson,et al.  Human lung tryptase. Purification and characterization. , 1984, The Journal of biological chemistry.

[32]  R. E. Edwards,et al.  Mast cells and inhalation of asbestos in rats. , 1984, Thorax.

[33]  M. Berridge Inositol trisphosphate and diacylglycerol as second messengers. , 1984, The Biochemical journal.

[34]  J. Pouysségur,et al.  Growth factor action and intracellular pH regulation in fibroblasts. Evidence for a major role of the Na+/H+ antiport. , 1984, The Journal of biological chemistry.

[35]  H. Hemker,et al.  Handbook of synthetic substrates : for the coagulation and fibrinolytic system , 1983 .

[36]  D. Seldin,et al.  Acid hydrolases and tryptase from secretory granules of dispersed human lung mast cells. , 1981, Journal of immunology.

[37]  W. Sherman,et al.  The effects of lithium ion and other agents on the activity of myo-inositol-1-phosphatase from bovine brain. , 1980, The Journal of biological chemistry.

[38]  L. Franzén,et al.  LOCAL MITOGENIC EFFECT OF TISSUE MAST CELL SECRETION , 1980, Cell and tissue kinetics.

[39]  K. Glenn,et al.  Thrombin active site regions required for fibroblast receptor binding and initiation of cell division. , 1980, The Journal of biological chemistry.

[40]  V. Ferrans,et al.  Ultrastructure of pulmonary mast cells in patients with fibrotic lung disorders. , 1979, Laboratory investigation; a journal of technical methods and pathology.

[41]  D. Carney,et al.  Cell surface action of thrombin is sufficient to initiate division of chick cells , 1978, Cell.

[42]  B. Zetter,et al.  Effects of protease treatment on growth, morphology, adhesion, and cell surface proteins of secondary chick embryo fibroblasts , 1976, Cell.

[43]  L. B. Chen,et al.  Mitogenic activity of blood components. I. Thrombin and prothrombin. , 1975, Proceedings of the National Academy of Sciences of the United States of America.

[44]  M. Aiba,et al.  Mast cells in the rat alveolar septa undergoing fibrosis after ionizing irradiation. Ultrastructural and histochemical studies. , 1974, Laboratory investigation; a journal of technical methods and pathology.

[45]  M. Burger Proteolytic Enzymes Initiating Cell Division and Escape from Contact Inhibition of Growth , 1970, Nature.