TGF-beta mRNA expression in cultured fibroblasts.
- Author:
Yong Ji RHO
;
Kyu Suk LEE
;
Joon Young SONG
- Publication Type:Original Article
- Keywords:
TGF-b mRNA;
Fibroblsts
- MeSH:
Amino Acids;
Blotting, Northern;
Collagen;
Dermis;
DNA, Complementary;
Embryonic Development;
Extracellular Matrix;
Fasciitis;
Female;
Fibroblasts*;
Fibrosis;
Humans;
Peptides;
Phenotype;
Pregnancy;
RNA, Messenger*;
Subcutaneous Tissue;
Transforming Growth Factor beta*;
Transforming Growth Factors;
Virtues
- From:Korean Journal of Dermatology
1992;30(6):824-829
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Transforming growth factor beta(TGF-p), initially identified in vlatelet extracts by virtue of its ability to confer anchorage of independent growth and a necplastic phenotype on mesenchymal cells, has subsequently been identified as a potent inh bit or of proliferation in most cells of epithelial origin. The family of TGF-p peptides is currenly onsisted of four subtypes (TGF-pl, p2, p3, p4). Tkiey are initially translated very larged are urssors of approximately 390 amino acids and produced by a wide variety of cell type. iricluding normal cells and tumor cells. TGF-ps promote deposition of extracellular matrix compcineits, facilitate remodeling events during embryonic development, and suppress immune ce 1 fimetion during the inflammatory process. Several nutaneous diseases are characterized typxcessive and progressive fibrosis of the dermis anil subcutaneous tissues. Prominent amon these disorders are progressive systemic sclerosi(PSS) and generalized morphea(GM), is well as the recently described syndrome of diffuse fasciitis eosinophilia(DF), also known; Shulmans syndrome. The hallmark of the pathologic alteration in these disorders is the excessive deposition of collagen and other connenctive iissues. Macromoleculse in the aerriis and/or the subcutaneous and fascial strutures often accompanied by variable degress of hronic inflammatory cell infiltrates. Now we have examined the expression of TGF-b1 mRNA using of northern blot hybridization with specific sequenced cDNA probe in the normal curltured fibroblasts, placental tissues, and fibrosarcorna derived tumor cell line(HT1080). We found that the size of TGF-b mRNA of each specimen was 2.5kb and theres no alteration of its quality.
