Published online before print February 21, 2002, doi: 10.1161/01.RES.0000013289.97650.C8
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© 2002 American Heart Association, Inc.
Molecular Medicine |
Characterization of the Mouse Aortic Carboxypeptidase-Like Protein Promoter Reveals Activity in Differentiated and Dedifferentiated Vascular Smooth Muscle Cells
From the Pulmonary and Critical Care (M.D.L., S.-F.Y., X.L., B.I., M.A.P.) and Cardiovascular (K.M., C.-M.H., M.-E.L.) Divisions and the Department of Medicine (M.D.L, S.-F.Y., C.-M.H., M.-E.L., M.A.P.), Brigham and Women’s Hospital and Harvard Medical School, Boston, Mass.
Correspondence to Matthew D. Layne, PhD, Brigham and Women’s Hospital, Pulmonary Division TH1333, 75 Francis St, Boston, MA 02115. E-mail mlayne{at}rics.bwh.harvard.edu
The dedifferentiation and proliferation of vascular smooth muscle cells (VSMCs) contribute to the formation of vascular lesions. In this study, the regulation of aortic carboxypeptidase-like protein (ACLP) expression in VSMCs was investigated. After mouse carotid injury, the expression of ACLP increases in the dedifferentiated VSMCs of the neointima in a pattern that differs from that of smooth muscle 
-actin. To better understand the regulation of ACLP in VSMCs, we characterized the 21-exon mouse ACLP gene and 5'-flanking region and examined its promoter activity. In transient transfection assays, 2.5 kb of the ACLP 5'-flanking sequence directed high levels of luciferase reporter activity in primary cultured rat aortic smooth muscle cells, and this activity was not dependent on serum response factor. We identified a positive element between base pairs -156 and -122 by analysis of 5' deletion and mutant constructs. By use of electrophoretic mobility shift assays with rat aortic smooth muscle cell nuclear extracts, Sp1 and Sp3 transcription factors bound to this region, and transfection assays in D.Mel.2 cells revealed that both Sp1 and Sp3 transactivated the ACLP promoter. Transgenic mice harboring the -2.5-kb ACLP promoter upstream from a nuclear-targeted LacZ gene were generated, and expression was detected in the VSMCs of large blood vessels, arterioles, and veins. Interestingly, ACLP promoter–LacZ reporter activity increased within the neointimal VSMCs of injured carotid vessels, consistent with the expression of the endogenous ACLP protein. The ACLP promoter may provide a novel tool to target gene expression to dedifferentiated VSMCs.
Key Words: vascular biology • carotid injury • aortic carboxypeptidase-like protein • transgene
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