Key result
Vascular smooth muscle cells from in stent stenosis and primary plaques overexpressed specific genes, including cell cycle regulatory and cell matrix proteins, compared to normal medial cells.
Observational
Gene expression profiles in ISS may guide target discovery; leaves open clinical relevance pending in vivo validation.
OBJECTIVE: We sought to identify differentially expressed genes in human in stent stenosis (ISS) to provide insights into the mechanism of disease. METHODS AND RESULTS: Using representation difference analysis, we examined differential gene expression between cultured normal human medial vascular smooth muscle cells (VSMCs) and cells from primary atherosclerotic plaques or ISS sites. Specific groups of genes were overexpressed in ISS and plaque VSMCs, including cell cycle regulatory proteins and cell matrix and contractile proteins. Differential expression was validated by virtual Northern analysis, reverse transcriptase-polymerase chain reaction, in situ hybridization, and immunohistochemistry. All ISS genes were expressed by normal intima and had even higher expression in primary plaque VSMCs. CONCLUSIONS: ISS VSMCs have a stable gene expression profile reflecting an intimal pattern, intermediate between normal medial and primary plaque VSMCs. Differential expression profiling may identify markers of disease that are overexpressed in ISS and also help elucidate the origin of the ISS lesion.
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Zhang et al. (2002) conducted an observational in In stent stenosis and primary atherosclerosis. In stent stenosis and primary atherosclerotic plaques vs. Normal human medial vascular smooth muscle cells was evaluated on Differential gene expression. Vascular smooth muscle cells from in stent stenosis and primary plaques overexpressed specific genes, including cell cycle regulatory and cell matrix proteins, compared to normal medial cells.
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