反义抑制质膜Ca2+泵诱导血管平滑肌细胞凋亡

Satoshi Sasamura , Ken-Ichi Furukawa , Miwa Shiratori , Shigeru Motomura , Yasushi Ohizumi
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引用次数: 25

摘要

研究了质膜Ca2+泵送atp酶(PMCA)反义寡脱氧核苷酸(ODNs)对原代培养大鼠主动脉血管平滑肌细胞(VSMCs)的影响。在培养的VSMCs中,超过80%的PMCA表达为PMCA- 1b亚型。暴露于针对PMCA-1的反义ODNs中,不仅PMCA蛋白的表达减少,PMCA- 1b mRNA的表达也呈浓度依赖性减少。通过PMCA催化的细胞外Na+独立45Ca2+外排被反义odn抑制。反义odn增加了静息和离子霉素或atp刺激的细胞内Ca2+水平。此外,长期使用反义odn可引起VSMCs的凋亡。有效的免疫抑制剂FK506可抑制细胞凋亡的发生。这些结果表明,PMCA被反义odn特异性抑制,并提示PMCA在调节细胞内Ca2+浓度中起重要作用,特别是在静息状态下,以防止可能通过钙调磷酸酶激活诱导的细胞凋亡的发生。
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Antisense-Inhibition of Plasma Membrane Ca2+ Pump Induces Apoptosis in Vascular Smooth Muscle Cells

The effect of antisense oligodeoxynucleotides (ODNs) of plasma membrane Ca2+-pumping ATPase (PMCA) on rat aortic vascular smooth muscle cells (VSMCs) in primary culture was examined. More than 80% of the PMCA expressed in cultured VSMCs was the PMCA-1B subtype. Exposed to antisense ODNs against PMCA-1, not only the expression of the PMCA protein but also mRNA of PMCA-1B was diminished in a concentration-dependent manner. Extracellular Na+-independent 45Ca2+ efflux catalyzed via PMCA was inhibited with antisense ODNs. Both the resting and ionomycin- or ATP-stimulated levels of intracellular Ca2+ were increased by antisense ODNs. Furthermore, prolonged treatment with antisense ODNs caused apoptosis in VSMCs. The occurrence of apoptosis was inhibited by FK506, a potent immunosuppressant. These results demonstrate that the PMCA was specifically inhibited by antisense ODNs and suggest that PMCA plays an important role in regulation of intracellular Ca2+ concentrations, especially at the resting condition to prevent an occurrence of apoptosis that may be induced through the activation of calcineurin.

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