诱导血红素氧合酶-1及雷帕霉素对PDGF诱导的大鼠平滑肌细胞表型转化的抑制作用
HO-1 and rapamycin inhibit phenotype transformation in smooth muscle cells of rats
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摘要: 目的 观察血红素氧合酶-1(HO-1)与雷帕霉素对血小板源性生长因子-BB(PDGF-BB)诱导的大鼠血管平滑肌细胞(VSMCs)表型转化的作用。方法 原代大鼠VSMCs给予PDGF-BB诱导表型转化。同时给予不同剂量的血红素氧合酶诱导剂氯血红素诱导HO-1的表达,和雷帕霉素共培养24h。结果 PDGF-BB20nmol/ml作用原代VSMCs24h后,SM-α-actin与PCNA表达减弱,PCNA表达增强。氯血红素诱导HO-1后可以抑制PDGF-BB诱导的VSMCs表型改变,并且随剂量的增加,抑制强度增加。较低剂量的雷帕霉素可以抑制PDGF诱导的VSMCs表型转化。结论 PDGF-BB亚型可以促进原代培养的大鼠VSMCs由收缩表型向合成表型转化,给予氯血红素诱导HO-1表达可以对抗PDGF-BB诱导的大鼠VSMCs表型转化,并呈剂量相关。Abstract: Objective To observe the inhibitory effect of HO-1 and rapamycin on PDGF-BB-induced phenotype transformation in vascular smooth muscle cells(VSMC)of rats. Methods Phenotype transformation was induced by PDGF-BB in primary rat aorta VSMC.Expression of HO-1 was induced with different doses of PDGF-BB.The cells were cultured with HO-1 and rapamycin for 24h. Results Twenty-four hours after phenotype transformation in VSMC of rats was induced with PDGF-BB,the expression of SM-α-actin was down-regulated while the expression of PCNA was up-regulated.Hemin-induced HO-1 suppressed PDGF-BB-induced expression of VSMC in a dose-dependent manner.Low dose rapamycin could inhibit PDGF-induced phenotype transformation in VSMC. Conclusion PDGF-BB subtype can promote the transformation of contraction phenotype to synthetic phenotype in VSMC.Hemin-induced HO-1 can inhibit PDGF-BB-induced phenotypic transformation in VSMC in a dose-dependent manner.
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