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Heat Shock Protein 90 Inhibitor Decreases Collagen Synthesis of Keloid Fibroblasts and Attenuates the Extracellular Matrix on the Keloid Spheroid Model

Title
Heat Shock Protein 90 Inhibitor Decreases Collagen Synthesis of Keloid Fibroblasts and Attenuates the Extracellular Matrix on the Keloid Spheroid Model
Author
윤채옥
Keywords
KINASE; HSP90; PATHOGENESIS; EXPRESSION; PATHWAY; DISEASE; SCAR; P38; PROLIFERATION; ACTIVATION
Issue Date
2015-09
Publisher
LIPPINCOTT WILLIAMS & WILKINS
Citation
PLASTIC AND RECONSTRUCTIVE SURGERY, v. 136, NO 3, Page. 328-337
Abstract
Background: The 90-kDa heat-shock protein (heat-shock protein 90) is an abundant cytosolic chaperone, and inhibition of heat-shock protein 90 by 17-allylamino-17-demethoxygeldanamycin (17-AAG) compromises transforming growth factor (TGF)--mediated transcriptional responses by enhancing TGF- receptor I and II degradation, thus preventing Smad2/3 activation. In this study, the authors evaluated whether heat-shock protein 90 regulates TGF- signaling in the pathogenesis and treatment of keloids. Methods: Keloid fibroblasts were treated with 17-AAG (10 M), and mRNA levels of collagen types I and III were determined by real-time reverse- transcriptase polymerase chain reaction. Also, secreted TGF-1 was assessed by enzyme-linked immunosorbent assay. The effect of 17-AAG on protein levels of Smad2/3 complex was determined by Western blot analysis. In addition, in 17-AAG-treated keloid spheroids, the collagen deposition and expression of major extracellular matrix proteins were investigated by means of Masson trichrome staining and immunohistochemistry. Results: The authors found that heat-shock protein 90 is overexpressed in human keloid tissue compared with adjacent normal tissue, and 17-AAG decreased mRNA levels of type I collagen, secreted TGF-ss 1, and Smad2/3 complex protein expression in keloid fibroblasts. Masson trichrome staining revealed that collagen deposition was decreased in 17-AAG-treated keloid spheroids, and immunohistochemical analysis showed that expression of collagen types I and III, elastin, and fibronectin was markedly decreased in 17-AAG-treated keloid spheroids. Conclusion: These results suggest that the antifibrotic action of heat-shock protein 90 inhibitors such as 17-AAG may have therapeutic effects on keloids.
URI
http://ovidsp.tx.ovid.com/sp-3.25.0a/ovidweb.cgi?QS2=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://hdl.handle.net/20.500.11754/27768
ISSN
0032-1052; 1529-4242
DOI
10.1097/PRS.0000000000001538
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COLLEGE OF ENGINEERING[S](공과대학) > BIOENGINEERING(생명공학과) > Articles
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