Note to users. If you're seeing this message, it means that your browser cannot find this page's style/presentation instructions -- or possibly that you are using a browser that does not support current Web standards. Find out more about why this message is appearing, and what you can do to make your experience of our site the best it can be.


Science 18 March 1983:
Vol. 219. no. 4590, pp. 1329 - 1331
DOI: 10.1126/science.6572416

Articles

Science, Vol 219, Issue 4590, 1329-1331
Copyright © 1983 by American Association for the Advancement of Science


articles

Polypeptide transforming growth factors isolated from bovine sources and used for wound healing in vivo

MB Sporn, AB Roberts, JH Shull, JM Smith, JM Ward, and J Sodek

Transforming growth factors, which are polypeptides that induce the transformed phenotype in nonneoplastic cells, have been isolated in bulk amounts from bovine salivary gland and kidney. In experiments in which wound healing chambers were implanted subcutaneously in the backs of rats, these bovine transforming growth factors accelerated the accumulation of total protein, collagen, and DNA in treated chambers. These studies thus show an effect of an isolated transforming growth factor in vivo.


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES:
Integrin-Mediated Transforming Growth Factor-{beta} Activation, a Potential Therapeutic Target in Fibrogenic Disorders.
S. L. Nishimura (2009)
Am. J. Pathol. 175, 1362-1370
   Abstract »    Full Text »    PDF »
Review of the activation of TGF-{beta} in immunity.
A. W. Taylor (2009)
J. Leukoc. Biol. 85, 29-33
   Abstract »    Full Text »    PDF »
The Effect of Growth Factors on Biomechanical Properties of the Bone-Patellar Tendon-Bone Graft After Anterior Cruciate Ligament Reconstruction: A Canine Model Study.
K. Yasuda, F. Tomita, S. Yamazaki, A. Minami, and H. Tohyama (2004)
Am. J. Sports Med. 32, 870-880
   Abstract »    Full Text »    PDF »
Interference with Transforming Growth Factor-{beta}/ Smad3 Signaling Results in Accelerated Healing of Wounds in Previously Irradiated Skin.
K. C. Flanders, C. D. Major, A. Arabshahi, E. E. Aburime, M. H. Okada, M. Fujii, T. D. Blalock, G. S. Schultz, A. Sowers, M. A. Anzano, et al. (2003)
Am. J. Pathol. 163, 2247-2257
   Abstract »    Full Text »
TGF{beta} is active, and correlates with activators of TGF{beta}, following porcine coronary angioplasty.
J. Chamberlain, J. Gunn, S. E. Francis, C. M. Holt, N. D. Arnold, D. C. Cumberland, M. W.J. Ferguson, and D. C. Crossman (2001)
Cardiovasc Res 50, 125-136
   Abstract »    Full Text »    PDF »
Connective tissue growth factor mediates transforming growth factor {beta}-induced collagen synthesis: down-regulation by cAMP.
M. R. DUNCAN, K. S. FRAZIER, S. ABRAMSON, S. WILLIAMS, H. KLAPPER, X. HUANG, and G. R. GROTENDORST (1999)
FASEB J 13, 1774-1786
   Abstract »    Full Text »
Effects of Transforming Growth Factor-beta (Isoforms 1-3) on Amyloid-beta Deposition, Inflammation, and Cell Targeting in Organotypic Hippocampal Slice Cultures.
M. E. Harris-White, T. Chu, Z. Balverde, J. J. Sigel, K. C. Flanders, and S. A. Frautschy (1998)
J. Neurosci. 18, 10366-10374
   Abstract »    Full Text »    PDF »
Periodontal Ligament Cells are Chemotactic to Fibroblast Collagenase.
V.P. Terranova and F. Nishimura (1996)
Journal of Dental Research 75, 993-1001
   Abstract »    PDF »
Effects of Tumor Necrosis Factor {alpha} and Vascular Permeability Factor on Neovascularization of the Rabbit Ear Flap.
D. W. Stepnick, M. K. Peterson, C. Bodgan, J. Davis, J. Wasman, and K. Mailer (1995)
Arch Otolaryngol Head Neck Surg 121, 667-672
   Abstract »    PDF »
Neutralisation of TGF-beta 1 and TGF-beta 2 or exogenous addition of TGF-beta 3 to cutaneous rat wounds reduces scarring.
M Shah, D. Foreman, and M. Ferguson (1995)
J. Cell Sci. 108, 985-1002
   Abstract »    PDF »
Collagen matrices attenuate the collagen-synthetic response of cultured fibroblasts to TGF-beta.
R. Clark, L. Nielsen, M. Welch, and J. McPherson (1995)
J. Cell Sci. 108, 1251-1261
   Abstract »    PDF »
A Contemporary View of Salivary Research.
I. D. Mandel (1993)
Critical Reviews in Oral Biology & Medicine 4, 599-604
   Abstract »    Full Text »    PDF »
Role of Growth Factors in Cutaneous Wound Healing: A Review.
C. P. Kiritsy and S. E. Lynch (1993)
Critical Reviews in Oral Biology & Medicine 4, 729-760
   Abstract »    Full Text »    PDF »
Epidermal Growth Factor in Cutaneous Repair Processes.
G. Ricotti, M.G. Tucci, A. Pugnaloni, G. Biagini, A. Belligolli, A. Bertani, R. Castagnani, and C. Castaldini (1992)
Journal of Bioactive and Compatible Polymers 7, 65-81
   Abstract »    PDF »
Concepts of Osteoblast Growth and Differentiation: Basis for Modulation of Bone Cell Development and Tissue Formation.
J. B. Lian and G. S. Stein (1992)
Critical Reviews in Oral Biology & Medicine 3, 269-305
   Abstract »    Full Text »    PDF »
Lack of Effects of Viral Sialoadenitis and Depletion of Epidermal Growth Factor on Initiation of Hepatic Carcinogenesis in the Rat.
D. R. Kemp, D. H. Percy, and M. A. Hayes (1991)
Toxicol Pathol 19, 156-163
   Abstract »    PDF »
Extracellular Matrix Molecules and their Receptors: An Overview with Special Emphasis on Periodontal Tissues.
V.-J. Uitto and H. Larjava (1991)
Critical Reviews in Oral Biology & Medicine 2, 323-354
   Abstract »    Full Text »    PDF »
Mediation of wound-related Rous sarcoma virus tumorigenesis by TGF-beta.
M. Sieweke, N. Thompson, M. Sporn, and M. Bissell (1990)
Science 248, 1656-1660
   Abstract »    PDF »
Mesenchymal Cell Growth Factors.
D. T. Graves and D. L. Cochran (1990)
Critical Reviews in Oral Biology & Medicine 1, 17-36
   Full Text »    PDF »
Characterization of Wound Cytokines in the Sponge Matrix Model.
H. R. Ford, R. A. Hoffman, E. J. Wing, D. M. Magee, L. McIntyre, and R. L. Simmons (1989)
Arch Surg 124, 1422-1428
   Abstract »    PDF »
An organ culture model for assaying wound repair of the fibrocartilaginous knee joint meniscus.
R. J. Webber, J. L. York, J. L. Vanderschilden, and A. J. Hough JR (1989)
Am. J. Sports Med. 17, 393-400
   Abstract »    PDF »
Angiotropin Treatment Prevents Flap Necrosis and Enhances Dermal Regeneration in Rabbits.
M. Hockel and J. F. Burke (1989)
Arch Surg 124, 693-698
   Abstract »    PDF »
Potential Roles of Fibronectin in Cutaneous Wound Repair.
R. A. F. Clark (1988)
Arch Dermatol 124, 201-206
   Abstract »    PDF »
Accelerated healing of incisional wounds in rats induced by transforming growth factor-beta.
T. Mustoe, G. Pierce, A Thomason, P Gramates, M. Sporn, and T. Deuel (1987)
Science 237, 1333-1336
   Abstract »    PDF »
Mitogenic Activity of Cementum Components to Gingival Fibroblasts.
Y. Miki, A.S. Narayanan, and R.C. Page (1987)
Journal of Dental Research 66, 1399-1403
   Abstract »    PDF »
Reversible inhibition of mammary gland growth by transforming growth factor-beta.
G. Silberstein and C. Daniel (1987)
Science 237, 291-293
   Abstract »    PDF »
Porous Collagen Sponge Wound Dressings: in vivo and in vitro Studies.
C. J. Doillon (1987)
J Biomater Appl 2, 562-578
   Abstract »    PDF »
Inhibition of endothelial regeneration by type-beta transforming growth factor from platelets.
R. Heimark, D. Twardzik, and S. Schwartz (1986)
Science 233, 1078-1080
   Abstract »    PDF »
Transforming growth factor-beta: biological function and chemical structure.
M. Sporn, A. Roberts, L. Wakefield, and R. Assoian (1986)
Science 233, 532-534
   Abstract »    PDF »
Development of Mullerian Inhibiting Substance as an Anti-cancer Drug.
R.L. Cate, E.G. Ninfa, D.J. Pratt, D.T. MacLaughlin, and P.K. Donahoe (1986)
Cold Spring Harb Symp Quant Biol 51, 641-647
   Abstract »    PDF »
Structure of a mouse submaxillary messenger RNA encoding epidermal growth factor and seven related proteins.
J Scott, M Urdea, M Quiroga, R Sanchez-Pescador, N Fong, M Selby, W. Rutter, and G. Bell (1983)
Science 221, 236-240
   Abstract »    PDF »



To Advertise     Find Products


Science. ISSN 0036-8075 (print), 1095-9203 (online)