Differential collagen I gene expression in fetal fibroblasts

Journal of Pediatric Surgery

Volumn 32, Issue 7, 1997, Pages 1033-1036

  Gallivan, Kerry ^b   Alman, Benjamin A ^b   Moriarty, Kevin P ^b   Pajerski, Mandy E ^b   O'Donnell, Cathleen ^b   Crombleholme, Timothy M ^a  

^a CHILDREN S HOSPITAL OF PHILADELPHIA   (United States)

^b NONE

Author keywords

Collagen; Fetal wound healing; Fibroblast; Reverse transcriptase polymerase chain reaction

Indexed keywords

COLLAGEN TYPE 1; TRANSFORMING GROWTH FACTOR BETA1;

CONFERENCE PAPER; EXTRACELLULAR MATRIX; FIBROBLAST; GENE EXPRESSION; GENETIC TRANSCRIPTION; HUMAN; HUMAN CELL; IN SITU HYBRIDIZATION; NORTHERN BLOTTING; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SCAR FORMATION; SKIN FIBROSIS; SKIN INCISION; WOUND HEALING;

EID: 0030790949     PISSN: 00223468     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0022-3468(97)90393-6     Document Type: Conference Paper

References (29)

1. Adzick NS, Longaker MT: Scarless fetal healing: Therapeutic implications. Ann Surg 215:3-12, 1992
2. Longaker MT, Whitby DJ, Adzick NS, et al: Studies in fetal wound healing VI. Second and early third trimester fetal wounds demonstrate rapid collagen deposition without scar formation. J Pediatr Surg 25:63-69, 1990
3. Whitby DJ, Ferguson MWJ: The extracellular matrix of lip wounds in fetal, neonatal, and adult mice. Development 112:651-658, 1991
4. DePalma PL, Krummel TM, Durham LA, et al: Characterization and quantitation of wound matrix in the fetal rabbit. Matrix 9:224-230, 1989
5. Longaker MT, Chiu ES, Adzick NS, et al: Studies in fetal wound healing V: A prolonged presence of hyaluronic acid characterizes fetal wound fluid. Ann Surg 213:292-299, 1991
6. Lin RY, Sullivan KM, Argenta PA, et al: Scarless human fetal skin repair is intrinsic to the fetal fibroblast and occurs in the absence of an inflammatory response: In situ hybridization and immunohistochemical studies. Wound Rep Regen 2:297-305, 1994
7. Moriarty KP, Crombleholme TM, Gallivan EK, et al: Hyaluronic acid-dependent pericellular matrices in fetal fibroblasts: Implications for scar-free wound repair. Wound Rep 4:346-352, 1996
8. Moriarty KP, Crombleholme TM: Differential fibroblast chemotaxis in fetal, neonatal, and adult cell lines in response to TGF-β1 and fetal bovine serum. Surg Forum 44:679-681, 1995
9. Gallivan EK, Crombleholme TM, O'Donnell C, et al: Induction of a fetal pattern of migration in postnatal fibroblasts by TGF-β3. Poster presentation at the American Pediatric Surgical Association, May 21, 1996, San Diego, CA
10. Moriarty KP, Crombleholme TM, Gallivan EK, et al: PDGF induces age and dose dependent differential fibroblast chemotaxis in fetal, neonatal, and adult cell lines in fetal bovine serum. Surg Forum 47:770-772, 1996
11. Chen WYJ, Grant MF, Schor AM, et al: Differences between adult and foetal fibroblasts in the regulation of hyaluronate synthesis: Correlation with migratory activity. J Cell Sci 94:577-584, 1989
12. Motsura H, Hakomori SF: The oncofetal domain of fibronectin defined by a monoclonal antibody FDC-6: Its presence in fetal and tumor tissues and its absence in those from normal tissue and plasma. Proc Natl Acad Sci U S A 83:6517-6521, 1985
13. Castellani P, Siri A, Rosellini C, et al: Transformed cells release different fibronectin variants than do normal cells. J Cell Biol 103:1671-1678, 1986
14. Bartal AH, Lichtig C, Cordon-Cardo C, et al: Monoclonal antibody defining fibroblasts appearing in fetal and neoplastic tissues. J Natl Cancer Inst 76:415-419, 1986
15. Sporn MB, Roberts AB, Wakefield LM, et al: Transforming growth factor-beta: Biological function and chemical structure. J Cell Biol 105:1039-1046, 1989
16. Roberts AB, Heine UI, Flanders KC, et al: Transforming growth factor-beta: Major role in regulation of the extracellular matrix. Ann N Y Acad Sci 580:225-232, 1990
17. Olutoye OO, Yager DR, Diegelmann RF, et al: Fetal pig platelets contain lower levels of TGF-β1, TGF-β2, and PDGF-AB: A possible explanation for reduced scarring in the fetus. Surg Forum 45:755-757, 1994
18. Lin RY, Sullivan KM, Argenta PA, et al: Exogenous transforming growth factor-beta amplifies its own expression and induces scar formation in a model of human fetal skin repair. Ann Surg 222:146-154, 1995
19. Kikuchi K, Kodano T, Ihn H, et al: Growth regulation in scleroderma fibroblasts: Increased response to transforming growth factor-beta. J Invest Dermatol 105:128-132, 1995
20. Pierce GF, Tarpley JE, Yanagihara D, et al: Platelet derived growth factor (BB homodimer), transforming growth factor-beta, and basic fibroblast growth factor in dermal wound healing: Neovessel and matrix formation and cessation of repair. Am J Pathol 140:1375-1388, 1992
21. Border WA, Noble NA: Transforming growth factor-beta in tissue fibrosis. N Engl J Med 331:1286-1292, 1984
22. Gallivan EK, Crombleholme TM, Moriarty KP, et al: Differential TGF-β1 gene expression in fetal vs. adult wound clefts. Surg Forum 47:767-769, 1996
23. Albini A, Pontz B, Pulz M, et al: Decline of fibroblast chemotaxis with age of donor cell passage number. Collagen Rel Res 1:23-37, 1988
24. Lorenz HP, Chang J, Longaker MT, et al: Transforming growth factor β1 and β2 synergistically increase gene expression of collagen types I and III in fetal but not adult fibroblasts. Surg Forum 44:723-725, 1993
25. Nath RK, Parks WC, Mackinnon SE, et al: The regulation of collagen in fetal skin wounds: mRNA localization and analysis. J Pediatr Surg 29:855-862, 1994
26. Sullivan KM, Lorenz HP, Meuli M, et al: A model of scarless human fetal wound repair is deficient in transforming growth factor beta. J Pediatr Surg 27:945-979, 1992
27. Whitby DJ, Ferguson MWJ: Immunohistochemical localization of growth factors in fetal wound healing. Dev Biol 147:207-215, 1991
28. Van Obberghen-Schilling E, Roche NS, Flanders KC, et al: Transforming growth factor beta positively regulates its own expression in normal and transformed cells. J Biol Chem 263:7741-7746, 1988
29. Roberts AB, Sporn MB, Assoian RK, et al: Transforming growth factor type β: Rapid induction of fibrosis and angiogenesis in vivo and stimulation of collagen formation in vitro. Proc Natl Acad Sci U S A 83:4167-4171, 1986