The effects of TGF-α, IL-1β and PDGF on fibroblast adhesion to ECM-derived matrix and KGF gene expression

Biomaterials

Volumn 31, Issue 9, 2010, Pages 2542-2548

  Wang, Xintong ^a   Waldeck, Heather ^b   Kao, Weiyuan J ^a,b,c  

^a UNIVERSITY OF WISCONSIN MADISON   (United States)

^b University of Wisconsin Madison   (United States)

^c UNIVERSITY OF WISCONSIN SCHOOL OF MEDICINE AND PUBLIC HEALTH   (United States)

Author keywords

Granulocyte macrophage colony stimulating factor; Interleukin 1 ; Interpenetrating network; Keratinocyte growth factor; Platelet derived growth factor BB; Transforming growth factor

Indexed keywords

GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTORS; INTERLEUKIN-1; INTERPENETRATING NETWORKS; KERATINOCYTE GROWTH FACTORS; PLATELET-DERIVED GROWTH FACTORS; TRANSFORMING GROWTH FACTORS;

ADHESION; BLOOD SUBSTITUTES; BODY FLUIDS; CELL CULTURE; ENZYME ACTIVITY; FIBROBLASTS; INTERPENETRATING POLYMER NETWORKS; MACROPHAGES; PEPTIDES; PLATELETS; TISSUE; TRANSCRIPTION;

BIOACTIVITY;

GRANULOCYTE MACROPHAGE COLONY STIMULATING FACTOR; INTERLEUKIN 1BETA; KERATINOCYTE GROWTH FACTOR; PLATELET DERIVED GROWTH FACTOR; TRANSFORMING GROWTH FACTOR ALPHA;

ARTICLE; CELL ADHESION; CONTROLLED STUDY; CYTOKINE RELEASE; EXTRACELLULAR MATRIX; GENE EXPRESSION; HUMAN; HUMAN CELL; MOLECULAR MECHANICS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN FUNCTION; PROTEIN SECRETION; PROTEIN SYNTHESIS; SKIN FIBROBLAST;

CELL ADHESION; CELL COUNT; CULTURE MEDIA, SERUM-FREE; DERMIS; EXTRACELLULAR MATRIX; FIBROBLAST GROWTH FACTOR 7; FIBROBLASTS; FIBRONECTINS; GENE EXPRESSION REGULATION; GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR; HUMANS; INTERLEUKIN-1BETA; PEPTIDES; PLATELET-DERIVED GROWTH FACTOR; POLYSTYRENES; RNA, MESSENGER; SERUM; TRANSFORMING GROWTH FACTOR ALPHA;

EID: 74449092219     PISSN: 01429612     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.biomaterials.2009.12.018     Document Type: Article

References (42)

1. Finch P.W., and Rubin J.S. Keratinocyte growth factor/fibroblast growth factor 7, a homeostatic factor with therapeutic potential for epithelial protection and repair. Adv Cancer Res 91 (2004) 69-136
2. Ornitz D.M., and Itoh N. Fibroblast growth factors. Genome Biol 2 reviews 3005.1-3005.12 (2001)
3. Beenken A., and Mohammadi M. The FGF family: biology, pathophysiology and therapy. Nat Rev Drug Discov 8 (2009) 235-253
4. Werner S., Krieg T., and Smola H. Keratinocyte-fibroblast interactions in wound healing. J Invest Dermatol 127 (2007) 998-1008
5. Mass-Szabowski N., Shimotoyodome A., and Fusenig N.E. Keratinocyte growth regulation in fibroblast cocultures via a double paracrine mechanism. J Cell Sci 112 (1999) 1843-1853
6. Witte R.P., and Kao W.J. Keratinocyte-fibroblast paracrine interaction: the effect of substrate and culture condition. Biomaterials 26 (2005) 3673-3682
7. Werner S. Keratinocyte growth factor: a unique player in epithelial repair processes. Cytokine Growth Factor Rev 9 (1998) 153-165
8. Niu J., Chang Z., Peng B., Xia Q., Lu W., Huang P., et al. Keratinocyte growth factor/fibroblast growth factor-7-regulated cell migration and invasion through activation of NF-κB transcription factors. J Biol Chem 282 (2007) 6001-6011
9. Putnins E.E., Firth J.D., and Uitto V.J. Stimulation of collagenase (MMP-1) synthesis in histiotypic epithelial cell culture by heparin and heparan sulfate with further stimulation by KGF. Matrix Biol 15 (1996) 21-29
10. Putnins E.E., Firth J.D., and Uitto V.J. Keratinocyte growth factor stimulation of gelatinase (MMP-9) and plasminogen activator (uPA) in histiotypic epithelial cell culture. J Invest Dermatol 104 (1995) 989-994
11. Brauchle M., Angermeyer K., Hübner G., and Werner S. Large induction of keratinocyte growth factor expression by serum growth factors and pro-inflammatory cytokines in cultured fibroblasts. Oncogene 9 (1994) 3199-3204
12. Chedid M., Rubin J.S., Csaky K.G., and Aaronson S.A. Regulation of keratinocye growth factor gene expression by Interleukin 1. J Biol Chem 269 (1994) 10753-10757
13. Weng J., Mohan R.R., Li Q., and Wilson S.E. IL-1 upregulates keratinocyte growth factor and hepatocyte growth factor mRNA and protein production by cultured stromal fibroblast cells: interleukin-1β expression in the cornea. Cornea 16 (1997) 465-471
14. Zander L., and Bemark M. Identification of genes deregulated during serum-free medium adaptation of a Burkitt's lymphoma cell line. Cell Prolif 41 (2008) 136-155
15. Jaluria P., Konstantopoulos K., Betenbaugh M., and Shiloach J. Egr1 and Gas6 facilitate the adaptation of HEK-293 cells to serum-free media by conferring enhanced viability and higher growth rates. Biotechnol Bioeng 99 (2008) 1443-1452
16. Massia S.P., and Hubbell J.A. An RGD spacing of 440 nm is sufficient for integrin αvβ3-mediated fibroblast spreading and 140 nm for focal contact and stress fiber formation. J Cell Biol 114 (1991) 1089-1100
17. Kao W.J., Lee D., Schense J.C., and Hubbell J.A. Fibronectin modulates macrophage adhesion and FBGC formation: the role of RGD, PHSRN, and PRRARV domains. J Biomed Mater Res 55 (2001) 79-88
18. Mann B.K., and West J.L. Cell adhesion peptides alter smooth muscle cell adhesion, proliferation, migration, and matrix protein synthesis on modified surfaces and in polymer scaffolds. J Biomed Mater Res 60 (2002) 86-93
19. Waldeck H., Chung A.S., and Kao W.J. Interpenetrating polymer networks containing gelatin modified with PEGylated RGD and soluble KGF: synthesis, characterization, and application in in vivo critical dermal wound. J Biomed Mater Res A 82 (2007) 861-871
20. Chung A.S., Gao Q., and Kao W.J. Either integrin subunit β1 or β3 is involved in Mediating monocyte adhesion, IL-1β protein and mRNA expression in response to surfaces functionalized with fibronectin-derived peptides. J Biomater Sci Polym Ed 18 (2007) 713-729
21. Gao Q., Chung A.S., and Kao W.J. Monocytic U937 adhesion, tumor necrosis factor-alpha and interleukin-1beta expression in response to gelatin-based networks grafted with arginine-glycine-aspartic acid and proline-histidine-serine-arginine-asparagine oligopeptides. Tissue Eng 13 (2007) 179-185
22. Kleinbeck K.R., Faucher L., and Kao W.J. Multifunctional in situ photopolymerized semi-interpenetrating network system is an effective donor site dressing: a cross comparison study in a swine model. J Burn Care Res 30 (2009) 37-45
23. Burmania J.A., Martinez-Diaz G.J., and Kao W.J. Synthesis and physicochemical analysis of interpenetrating networks containing modified gelatin and poly(ethylene glycol) diacrylate. J Biomed Mater Res A 67 (2003) 224-234
24. Shearer H., Ellis M.J., Perera S.P., and Chaudhuri J.B. Effects of common sterilization methods on the structure and properties of poly(D,L lactic-coglycolic acid) scaffolds. Tissue Eng 12 (2006) 2717-2727
25. Rozen S., and Skaletsky H.J. Primer3 on the WWW for general users and for biologist programmers. In: Krawetz S., and Misener S. (Eds). Bioinformatics methods and Protocols: methods in molecular biology (2000), Humana Press, Totowa, NJ 365-386
26. Radonić A., Thulke S., Mackay I.M., Landt O., Siegert W., and Nitsche A. Guideline to reference gene selection for quantitative real-time PCR. Biochem Biophys Res Commun 313 (2004) 856-862
27. Rasband WS, ImageJ, U.S. National Institutes of Health, Bethesda, MD. Online. 1997-2008. Available from URL: http://rsb.info.nih.gov/ij.
28. Sasaki M., Kashima M., Ito T., Watanabe A., Izumiyama N., Sano M., et al. Differential regulation of metalloproteinase production, proliferation and chemotaxis of human lung fibroblasts by PDGF, interleukine-1β and TNF-α. Mediators Inflamm 9 (2000) 155-160
29. Yamamoto M., Aoyagi M., Fukai N., Matsushima Y., and Yamamoto K. Differences in cellular responses to mitogens in arterial smooth muscle cells derived from patients with moyamoya disease. Stroke 29 (1998) 1188-1193
30. Bronson R.E., Argenta J.G., and Bertolami C.N. Interleukin-1-induced changes in extracellular glycosaminoglycan composition of cutaneous scar-derived fibroblasts in culture. Coll Relat Res 8 (1988) 199-208
31. Bronson R.E., Bertolami C.N., and Siebert E.P. Modulation of fibroblast growth and glycosaminoglycan synthesis by interleukin-1. Coll Relat Res 7 (1987) 323-332
32. Denk P.O., Roth-Eichhorn S., Gressner A.M., and Knorr M. Cytokine regulation of hyaluronate production by human tenon's capsule fibroblasts. Curr Eye Res 20 (2000) 77-80
33. Brink H.E., Stalling S.S., and Nicoll S.B. Influence of serum on adult and fetal dermal firbroblast migration, adhesion and collagen expression. In Vitro Cell Dev Biol Anim 41 (2005) 252-257
34. 2+increase, mitogenic activity, and extracellular matrix production enhancement. Endocrinology 133 (1993) 1880-1890
35. Hynes R.O. Integrins: bidirectional, allosteric signaling machines. Cell 110 (2002) 673-687
36. Milam S.B., Magnuson V.L., Steffensen B., Chen D.L., and Klebe R.J. IL-1β and prostaglandins regulate integrin mRNA expression. J Cell Physiol 149 (1991) 173-183
37. Rinaldi N., Weis D., Brado B., Schwarz-Eywill M., Lukoschek M., Pezzutto A., et al. Differential expression and functional behaviour of the αv and β3 integrin subunits in cytokine stimulated fibroblast-like cells derived from synovial tissue of rheumatoid arthritis and osteoarthritis in vitro. Ann Rheum Dis 56 (1997) 729-736
38. Hoffman S., He S., Jin M., Ehren M., Wiedemann P., Ryan S.J., et al. A selective cyclic integrin antagonist blocks the integrin receptors αvβ3 and αvβ5 and inhibits retinal pigment epithelium cell attachment, migration and invation. BMC Ophthalmol 5 (2005) 16
39. Takizawa M., Hida T., Horiguchi T., Hiramoto A., Harada S., and Tanida S. TAN-1511 A, B and C, microbial lipopeptides with G-CSF and GM-CSF inducing activity. J Antibiot (Tokyo) 48 (1995) 579-588
40. Kamely D., and Rudland P.S. Induction of DNA synthesis and cell division in human diploid skin fibroblasts by fibroblast growth factor. Exp Cell Res 97 (1976) 120-126
41. Kaplan P.L., Anderson M., and Ozanne B. Transforming growth factor(s) production enables cells to grow in the absence of serum: an autocrine system. Proc Natl Acad Sci U S A 79 (1982) 485-489
42. Shaoul R., Eliahu L., Sher I., Hamlet Y., Miselevich I., Goldshmidt O., et al. Elevated expression of FGF7 protein is common in human gastric diseases. Biochem Biophys Res Commun 350 (2006) 825-833