Korean J Physiol Pharmacol.
1999 Dec;3(6):597-603.
The transfection of caldesmon DNA into primary cultured rat aortic vascular smooth muscle
- Affiliations
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- 1Department of Pharmacology, College of Medicine, Chungbuk National University, Cheongju, Chungbuk, Korea.
Abstract
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Caldesmon (CaD), one of microfilament-associated proteins, plays a key
role in microfilament assembly in mitosis. We have investigated the
effects of overexpression of the high molecular weight isoform of CaD
(h-CaD) on the physiology of vascular smooth muscle cells (VSMCs). Rat
aortic VSMCs were stably transfected with plasmids carrying a full
length human h-CaD cDNA under control of cytomegalovirus promoter. The
majority of the overexpressed h-CaD appears to be localized
predominantly on cytoskeleton structures as determined by detergent
lysis. The overexpression of h-CaD, however, does not decrease the
level of endogenous low molecular weight isoform of CaD. h-CaD
overexpressing VSMCs (h-CaD/VSMCs) show a decreased growth rate than
that of vector-only transfected cells when determined by (3H)thymidine
uptake and cell counting after fetal bovine serum (FBS) stimulation.
h-CaD/VSMCs were smaller than vector-transfected cells by 18% in cell
diameter. These data suggest that overexpression of h-CaD can inhibit
the poliferation and the cell volume of VSMCs stimulated by growth
factors and that the gene therapy with h-CaD may be helpful to prevent
the conditions associated with hypertrophy and/or hyperplasia of VSMCs
after arterial injuries.