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Circulation Research. 2001;88:30-36

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(Circulation Research. 2001;88:30.)
© 2001 American Heart Association, Inc.


Molecular Medicine

Transforming Growth Factor-ß/Smads Signaling Induces Transcription of the Cell Type–Restricted Ankyrin Repeat Protein CARP Gene Through CAGA Motif in Vascular Smooth Muscle Cells

Hiroyoshi Kanai, Toru Tanaka, Yasushi Aihara, Sin-ichi Takeda, Masahiro Kawabata, Kohei Miyazono, Ryozo Nagai, Masahiko Kurabayashi

From the Second Department of Internal Medicine (H.K., T.T., Y.A., M. Kurabayashi), Gunma University School of Medicine, Maebashi, Gunma, Japan; First Department of Internal Medicine (S.-i.T.), Tottori University School of Medicine, Yonago, Tottori, Japan; Department of Biochemistry (M. Kawabata, K.M.), The Cancer Institute, Tokyo, Japanese Foundation for Cancer Research, Toshima-ku, Tokyo, Japan; and Department of Cardiovascular Medicine (R.N.), University of Tokyo, Bunkyo-ku, Tokyo, Japan.

Correspondence to Masahiko Kurabayashi, MD, PhD, Second Department of Internal Medicine, Gunma University School of Medicine, 3-39-15 Showa-machi Maebashi, Gunma, 371-8511, Japan. E-mail mkuraba{at}med.gunma-u.ac.jp

Abstract—Transforming growth factor (TGF)-ß plays a major role in the development of vascular diseases. Despite the pleiotropic effects of TGF-ß on vascular smooth muscle cells (VSMCs), only a few genes have been characterized as direct targets of TGF-ß in VSMCs. Cardiac ankyrin repeat protein (CARP) has been thought to be expressed exclusively in the heart. In the present study, we showed that CARP is expressed in the vasculature after balloon injury and in cultured VSMCs in response to TGF-ß. Analysis of a half-life of the cytoplasmic CARP mRNA levels and the transient transfection of the CARP promoter/luciferase gene indicates that the regulation of CARP expression is increased by TGF-ß at the transcriptional level. Transfection of expression vectors encoding Smads significantly activated the CARP promoter/luciferase activity. Deletion analysis and site-specific mutagenesis of the CARP promoter indicate that TGF-ß response element is localized to CAGA motif at -108 bp relative to the transcription start site. Electrophoretic mobility shift assays showed that the binding activity to the CAGA motif was increased in nuclear extracts of cultured VSMCs by TGF-ß. Cells transfected with adenovirus vector expressing CARP showed a significant decrease in DNA synthesis. Overexpression of CARP enhanced the TGF-ß–mediated inhibition of the DNA synthesis. These data indicate that CARP is a downstream target of TGF-ß/Smad signaling in VSMCs and suggest a role of CARP in mediation of the inhibitory effects of TGF-ß on the proliferation of VSMCs.


Key Words: proteins • growth factors • cells • transcription • muscle, smooth




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