| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
American Journal of Pathology, Vol 142, 463-470, Copyright © 1993 by American Society for Investigative Pathology
REGULAR ARTICLES |
EM Tan, S Rouda, SS Greenbaum, JH Moore Jr, JW Fox 4th and S Sollberg
Department of Pathology, Thomas Jefferson University, Philadelphia, Pennsylvania.
The effects of acidic and basic fibroblast growth factors (FGFs) on collagen expression by keloid fibroblasts were examined in the absence and presence of heparin. Collagen biosynthesis and gene expression of type I collagen were down-regulated by the FGFs in the presence of heparin. Acidic FGF, in a concentration range of 0.4 to 50 ng/ml, had little or no effect on collagen synthesis after a 4-day incubation. However, in the presence of heparin (100 micrograms/ml) acidic FGF, in concentrations ranging from 2 to 50 ng/ml, decreased [3H]hydroxyproline synthesis by 44 to 68%, compared with untreated control cultures. Total [3H]hydroxyproline synthesis was similar between control and heparin- treated cultures. Basic FGF (2.0 to 50 ng/ml) was effective in suppressing [3H]hydroxyproline synthesis by 50 to 90% after a 4-day incubation without heparin in keloid and normal fibroblast cultures. The steady-state levels of type I collagen messenger RNA were significantly decreased by acidic FGF in the presence of heparin, as well as by basic FGF without heparin. The data suggest that the FGFs are effective in down-regulating excess collagen production by keloid fibroblasts and that this inhibitory effect is apparently associated with pretranslational events. Moreover, acidic FGF is apparently dependent on heparin, whereas basic FGF is not, for potentiation of the down-regulatory effects of the FGFs.
This article has been cited by other articles:
![]() |
M. M. Hanasono, J. Lum, L. A. Carroll, A. A. Mikulec, and R. J. Koch The Effect of Silicone Gel on Basic Fibroblast Growth Factor Levels in Fibroblast Cell Culture Arch Facial Plast Surg, March 1, 2004; 6(2): 88 - 93. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. M. Hanasono, M. Kita, A. A. Mikulec, D. Lonergan, and R. J. Koch Autocrine Growth Factor Production by Fetal, Keloid, and Normal Dermal Fibroblasts Arch Facial Plast Surg, January 1, 2003; 5(1): 26 - 30. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. J. Lim, T.-T. Phan, B.-H. Bay, R. Qi, H. Huynh, W. T.-L. Tan, S.-T. Lee, and M. T. Longaker Fibroblasts cocultured with keloid keratinocytes: normal fibroblasts secrete collagen in a keloidlike manner Am J Physiol Cell Physiol, July 1, 2002; 283(1): C212 - C222. [Abstract] [Full Text] [PDF] |
||||
![]() |
E. T. Cheng, K. C. Nowak, and R. J. Koch Effect of Blended Carbon Dioxide and Erbium:YAG Laser Energy on Preauricular and Ear Lobule Keloid Fibroblast Secretion of Growth Factors: A Serum-Free Study Arch Facial Plast Surg, October 1, 2001; 3(4): 252 - 257. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. C. McCormack, K. C. Nowak, and R. J. Koch The Effect of Copper Tripeptide and Tretinoin on Growth Factor Production in a Serum-Free Fibroblast Model Arch Facial Plast Surg, January 1, 2001; 3(1): 28 - 32. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. Vogelmann, D. Ruf, M. Wagner, G. Adler, and A. Menke Effects of fibrogenic mediators on the development of pancreatic fibrosis in a TGF-{beta}1 transgenic mouse model Am J Physiol Gastrointest Liver Physiol, January 1, 2001; 280(1): G164 - G172. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Becerril, A. Pardo, M. Montaño, C. Ramos, R. Ramírez, and M. Selman Acidic Fibroblast Growth Factor Induces an Antifibrogenic Phenotype in Human Lung Fibroblasts Am. J. Respir. Cell Mol. Biol., May 1, 1999; 20(5): 1020 - 1027. [Abstract] [Full Text] |
||||
![]() |
H. S. Chang, D. B. Hom, R. P. Agarwal, K. Pernell, J. C. Manivel, and C. Song Effects of Basic Fibroblast Growth Factor on Irradiated Porcine Skin Flaps Arch Otolaryngol Head Neck Surg, March 1, 1998; 124(3): 307 - 312. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. G. Pickering, C. M. Ford, B. Tang, and L. H. Chow Coordinated Effects of Fibroblast Growth Factor-2 on Expression of Fibrillar Collagens, Matrix Metalloproteinases, and Tissue Inhibitors of Matrix Metalloproteinases by Human Vascular Smooth Muscle Cells : Evidence for Repressed Collagen Production and Activated Degradative Capacity Arterioscler. Thromb. Vasc. Biol., March 1, 1997; 17(3): 475 - 482. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |