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Chinese Medical Journal ; (24): 166-170, 2003.
Article in English | WPRIM | ID: wpr-356842

ABSTRACT

<p><b>OBJECTIVE</b>To clone the full-length cDNA of a gene responsible for vascular smooth muscle cell (v-SMC) proliferation in atherogenesis, and study its function.</p><p><b>METHODS</b>Oxidized low density lipoprotein (ox-LDL) at optimal concentration was used as the stimulant to induce v-SMC proliferation in culture medium. A cDNA subtractive library of v-SMC proliferation specific to ox-LDL stimulation was established using subtractive hybridization technique. Methods, including blotting, Northern hybridization and gene sequencing, were used to clone new gene fragments. By using full-length cDNA screening and protein expression techniques, one full-length cDNA was cloned and its function was studied.</p><p><b>RESULTS</b>One full-length cDNA was cloned. The new gene (Genbank AF 174647) expressed a 44 kDa protein, which might be associated with the activity of ox-LDL.</p><p><b>CONCLUSION</b>The new gene cloned may be associated with SMC proliferation in atherogenesis.</p>


Subject(s)
Humans , Amino Acid Sequence , Arteriosclerosis , Genetics , Base Sequence , Blotting, Northern , Cell Division , Cells, Cultured , Cloning, Molecular , Gene Library , Lipoproteins, LDL , Pharmacology , Molecular Sequence Data , Muscle, Smooth, Vascular , Cell Biology , Nucleic Acid Hybridization
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