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Role of AP-1 complex in angiotensin II-mediated transforming growth factor-β expression and growth of smooth muscle cells:: Using decoy approach against AP-1 binding site
被引:52
作者:
Morishita, R
[1
]
Gibbons, GH
Horiuchi, M
Kaneda, Y
Ogihara, T
Dzau, VJ
机构:
[1] Harvard Univ, Sch Med, Div Cardiovasc Med, Boston, MA 02115 USA
[2] Osaka Univ, Sch Med, Dept Geriatr Med, Osaka, Japan
[3] Osaka Univ, Sch Med, Inst Cellular & Mol Biol, Osaka, Japan
关键词:
gene regulation;
HVJ-liposome transfer;
remodeling;
hypertension;
paracrine/autocrine;
D O I:
10.1006/bbrc.1997.8012
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The cis element double-stranded oligodeoxynucleotides (ODN) ("decoy") approach has enabled us to clarify the responsible elements. Using this approach, we transfected AP-1 decoy ODN into VSMC cultured from WKY rats (WKY Adu) which produce latent TGF-beta, but not active TGF-beta, and Sprague-Dawley rats (CNC) which produce active and latent TGF-beta under Ang II-stimulation. AP-1, but not mismatched, decoy ODN abolished Ang II-stimulated TGF-beta gene expression and production in both Adu and CNC. However, AP-1 decoy did not alter DNA, RNA, and protein synthesis in Adu. In contrast, cell. number was increased under Ang II stimulation by AP-1 decoy ODN in CNC without significant change in RNA and protein synthesis. These results showed that Ang II stimulated TGF-beta production through the AP-1 complex. In VSMC that produce active TGF-beta (CNC), the AP-1 complex stimulated by Ang II may inhibit cell growth through active TGF-beta production. Overall, this study demonstrates the utility of the decoy approach to study the specific function of cis elements in endogenous gene regulation such as Ang II-induced TGF-beta expression. (C) 1998 Academic Press.
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页码:361 / 367
页数:7
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