Mitogenic and Protein Synthetic Activity of Tissue Repair Cells: Control by the Postsurgical Macrophage

References

• Ryan G. G., Groberty J., Majro G. Mesothelial injury and recovery. Am J Pathol 1973; 71: 93–102
   PubMed Web of Science ®Google Scholar
• Buckman R. F., Buckman P. D., Hufnagel H. V., et al. A physiologic basis for the adhesion-free healing of deperitonealized surfaces. J Surg Res 1976; 21: 67–76
   PubMed Web of Science ®Google Scholar
• Leibovich S. J., Ross R. The role of the macrophage in wound repair. A study with hydrocortisone and antimacrophage serum. Am J Pathol 1975; 78: 71–91
   PubMed Web of Science ®Google Scholar
• Shimanuki T., Nakamura R. M., diZerega G. S. A kinetic analysis of peritoneal fluid cytology and arachidonic acid metabolism after abrasion and reabrasion of rabbit peritoneum. J Surg Res 1986; 41: 245–251
   PubMed Web of Science ®Google Scholar
• Orita H., Nakamura R. M., diZerega G. S. Kinetic analysis of proline and glucosamine by exudative and tissue repair cells. Surg Forum 1985; 36: 467–469
   Google Scholar
• Fukasawa M., Bryant S. M., diZerega G. S. Superoxide anion production by postsurgical macrophages. J Surg Res 1988; 45: 382–388
   PubMed Web of Science ®Google Scholar
• Fukasawa M., Campeau J. D., Girgis W., et al. Production of protease inhibitors by postsurgical macrophages. J Surg Res 1989; 46: 256–261
   PubMed Web of Science ®Google Scholar
• Fukasawa M., Bryant S. M., Nakamura R. M., et al. Modulation of fibroblast proliferation of postsurgical macrophages. J Surg Res 1987; 43: 513–520
   PubMed Web of Science ®Google Scholar
• Fukasawa M., Bryant S. M., diZerega G. S. Incorporation of thymidine by fibroblast: Evidence for complex regulation by postsurgical macrophages. J Surg Res, in press.
   Google Scholar
• Moses A. C., Cohen K. L., Johnson R. Baugh, et al. Contribution of human somatomedin activity to the serum growth requirement of human skin fibroblasts and chick embryo fibroblasts in culture. J Clin Endocrinol Metab 1978; 46: 937–946
   PubMed Web of Science ®Google Scholar
• Conovar C. A., Rosenfeld R. G., Hintz R. L. Hormonal control of the replication of human fetal fibroblasts: Role of somatomedin C/insulin-like growth factor I. J Cell Physiol 1986; 128: 47–54
   PubMed Web of Science ®Google Scholar
• Clemmons D. R., Shaw D. S. Purification and biologic properties of fibroblast somatomedin. J Biol Chem 1986; 261: 10, 293–310; 298
   Web of Science ®Google Scholar
• Gospodarowicz D., Neufield G., Schweigerer L. Molecular and biological characterization of fibroblast growth factor, an angiogenic of mesoderm and neuroectoderm-de-rived cells. Cell Different 1986; 19: 1–17
   PubMedGoogle Scholar
• Gospodarowicz D., Ferrara N., Schweigerer L., et al. Structural characterization and biological functions of fibroblast growth factor. Endocrine Rev 1987; 8: 95–114
   PubMed Web of Science ®Google Scholar
• Wiener S. L., Wiener R., Platt N. The need for modification of the polyvinyl sponge model of connective tissue growth: Histologic and biochemical studies in the rabbit. Connect Tissue Res 1975; 3: 213–225
   PubMed Web of Science ®Google Scholar
• Raferty A. T. Regeneration of parietal and visceral peritoneum. Br J Surg 1973; 60: 293–299
   PubMed Web of Science ®Google Scholar
• Raferty A. T. Regeneration of parietal and visceral peritoneum in the immature animal. Br J Surg 1973; 60: 969–975
   PubMed Web of Science ®Google Scholar
• Diegelmann R. F., Cohen I. K., Kaplan A. M. The role of macrophages in wound repair. Plast Reconst Surg 1981; 68: 107–113
   PubMed Web of Science ®Google Scholar
• Leibovich S. J. Production of macrophage-dependent fibroblast-stimulating activity(M-FSA) by murine macrophages: Effects on BALBc3T3 fibroblasts. Exp Cell Res 1978; 113: 47–56
   PubMed Web of Science ®Google Scholar
• Tchorzewski H., De nys A., Lipinski S. The influence of polymorphonuclear leukocytes and macrophages on the growth of lymphocytes and fibroblasts in vitro. Exp Path Bcl 1975; 10S: 289–293
   Google Scholar
• Martin B. M., Gimbrone MA, Jr, Unanue E. R., et al. Stimulation of nonlymphoid mesenchymal cell proliferation by a macrophage-derived growth factor. J Immunol 1981; 126: 1510–1515
   PubMed Web of Science ®Google Scholar
• Jimenez S. A., McArthur W., Rosenbloom J. Inhibition of collagen synthesis by mononuclear cell supernates. J Exp Med 1979; 150: 1421–1431
   PubMed Web of Science ®Google Scholar
• Gill P. J., Adler J., Silbert C. K., et al. Removal of glycosaminoglycans from cultures of human skin fibroblasts. Biochem J 1981; 194: 299–307
   PubMed Web of Science ®Google Scholar
• Roberts A. B., Anzano M. A., Wakefield L. M., et al. Type p transforming growth factor: A bifunctional regulator of cellular growth. Proc Natl Acad Sci USA 1985; 82: 119–123
   PubMed Web of Science ®Google Scholar
• Assoian R. K. Biphasic effect of type p transforming growth factor on epidermal growth factor receptors in NRK fibroblasts: Functional consequences for epidermal growth factor-stimulated mitosis. J Biol Chem 1986; 261: 9613–9617
   Google Scholar
• Ignotz R. A., Massague J. Transforming growth factor-β stimulated the expression of fibronectin and collagen and their incorporation into the extracellular matrix. J Biol Chem 1986; 261: 4337–4345
   PubMed Web of Science ®Google Scholar
• Ignotz R. A., Endo T., Massague J. Regulation of fibronectin and type I collagen mRNA levels by transforming growth factor-β. J Biol Chem 1987; 262: 6443–6446
   PubMed Web of Science ®Google Scholar
• Fukasawa M., Bryant S. M., Onta H., et al. Modulation of proline and glucosamine incorporation into tissue repair cells by peritoneal macrophages. J Surg Res 1989; 46: 166–171
   PubMed Web of Science ®Google Scholar
• Varga J., Jimenez S. A. Stimulation of normal human fibroblast collagen production and processing by transforming growth factor-β and 12-O-tetradecanoylphorbol-13-acetate. J Biol Chem 1987; 262: 2283–2290
   PubMedGoogle Scholar
• Tralacker F. M., Nilsen-Hamilton M. Specific induction of secreted proteins by transforming growth factor-β and 12-O-tetradecanoylphorbol-13-acetate. J Biol Chem 1987; 262: 2283–2290
   PubMed Web of Science ®Google Scholar
• Sporn M. B., Roberts A. B., Shull J. H., et al. Polypeptide transforming growth factors isolated from bovine sources and used for wound healing in vivo. Science 1983; 219: 1329–1331
   PubMed Web of Science ®Google Scholar
• Ross R., Bowen-Pope D. F. Platelet-derived growth factor. J Clin Endocrinol Metab 1984; 13: 191–205
   Google Scholar
• Ross R., Glomset J., Kariya B., et al. A platelet-dependent serum factor that stimulates the proliferation of arterial smooth muscle cells in vitro. Proc Nail Acad Sci USA 1974; 71: 1207–1210
   PubMed Web of Science ®Google Scholar
• Shimokado K., Raines E. W., Madtes D. K., et al. A significant part of macrophage-derived growth factor consists of at least two forms of PDGF. Cell 1985; 43: 277–286
   PubMed Web of Science ®Google Scholar
• Seppa H., Grotendorst G., Seppa S., et al. Platelet-derived growth factor is chemotactic for fibroblasts. J Cell Biol 1982; 92: 584–588
   PubMed Web of Science ®Google Scholar
• Wahl S. M., Wahl L. M., MacCarthy J. B. Lymphocyte-mediated activation of fibroblast proliferation and collagen production. J Immunol 1978; 121: 942–946
   PubMed Web of Science ®Google Scholar