Okura T, Igase M, Kitami Y, Fukuoka T, Maguchi M, Kohara K, Hiwada K
Second Department of Internal Medicine, Ehime University School of Medicine, Onsen-gun, Ehime 791-0295, Japan.
Biochim Biophys Acta. 1998 Jul 24;1403(3):245-53. doi: 10.1016/s0167-4889(98)00065-2.
Apoptosis (programmed cell death) is observed in vascular smooth muscle cells (VSMC) in atherosclerotic lesions and stenotic lesions after injury, and modulates the cellularity of these lesions. It is recognized that cell growth and apoptosis are two linked processes. Platelet-derived growth factor (PDGF) induces VSMC proliferation and migration in vitro. We studied the effect of PDGF on apoptosis in VSMC. Cultured rat VSMC were treated with PDGF-AA or PDGF-BB. PDGF-BB induced cell death in cultured VSMC in a time- and dose-dependent manner, but PDGF-AA did not. Gel electrophoresis of genomic DNA and in situ DNA labeling confirmed that the cell death induced by PDGF-BB is apoptosis. PDGF-BB treatment reduced bcl-2 mRNA and bcl-xl mRNA expression, in contrast, induced bcl-xs mRNA expression, linked with the induction of apoptosis in cultured VSMC.
在动脉粥样硬化病变和损伤后的狭窄病变中,血管平滑肌细胞(VSMC)会出现凋亡(程序性细胞死亡),并且这种凋亡会调节这些病变的细胞数量。人们认识到细胞生长和凋亡是两个相互关联的过程。血小板衍生生长因子(PDGF)在体外可诱导VSMC增殖和迁移。我们研究了PDGF对VSMC凋亡的影响。用PDGF-AA或PDGF-BB处理培养的大鼠VSMC。PDGF-BB以时间和剂量依赖的方式诱导培养的VSMC细胞死亡,但PDGF-AA则不会。基因组DNA的凝胶电泳和原位DNA标记证实,PDGF-BB诱导的细胞死亡是凋亡。与诱导培养的VSMC凋亡相关,PDGF-BB处理降低了bcl-2 mRNA和bcl-xl mRNA的表达,相反,却诱导了bcl-xs mRNA的表达。