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辛伐他汀对特发性肺动脉高压患者肺动脉平滑肌细胞血小板衍生生长因子信号的抑制作用。

Inhibitory effects of simvastatin on platelet-derived growth factor signaling in pulmonary artery smooth muscle cells from patients with idiopathic pulmonary arterial hypertension.

机构信息

Department of Cardiovascular Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama, Japan.

出版信息

J Cardiovasc Pharmacol. 2010 Jan;55(1):39-48. doi: 10.1097/FJC.0b013e3181c0419c.

Abstract

Idiopathic pulmonary arterial hypertension (IPAH) is a progressive disease characterized by inappropriate increase of pulmonary artery smooth muscle cells (PASMCs) leading to occlusion of pulmonary arterioles. Inhibition of platelet-derived growth factor (PDGF) signaling is starting to garner attention as a targeted therapy for IPAH. We assessed the inhibitory effects of simvastatin, a 3-hydroxy-3-methylglutanyl coenzyme A reductase inhibitor, on PDGF-induced proliferation and migration of PASMCs obtained from 6 patients with IPAH who underwent lung transplantation. PDGF stimulation caused a significantly higher growth rate of PASMCs from patients with IPAH than that of normal control PASMCs as assessed by (3)H-thymidine incorporation. Simvastatin (0.1 micromol/L) significantly inhibited PDGF-induced cell proliferation of PASMCs from patients with IPAH but did not inhibit proliferation of normal control cells at the same concentration. Western blot analysis revealed that simvastatin significantly increased the expression of cell cycle inhibitor p27. PDGF significantly increased the migration distance of IPAH-PASMCs compared with that of normal PASMCs, and simvastatin (1 micromol/L) significantly inhibited PDGF-induced migration. Immunofluorescence staining revealed that simvastatin (1 micromol/L) inhibited translocation of Rho A from the cytoplasm to membrane and disorganized actin fibers in PASMCs from patients with IPAH. In conclusion, simvastatin had inhibitory effects on inappropriate PDGF signaling in PASMCs from patients with IPAH.

摘要

特发性肺动脉高压(IPAH)是一种进行性疾病,其特征为肺动脉平滑肌细胞(PASMCs)的不适当增加,导致肺小动脉闭塞。血小板衍生生长因子(PDGF)信号抑制作为特发性肺动脉高压的靶向治疗开始受到关注。我们评估了辛伐他汀(3-羟基-3-甲基戊二酰辅酶 A 还原酶抑制剂)对 6 名接受肺移植的特发性肺动脉高压患者 PASMCs 中 PDGF 诱导的增殖和迁移的抑制作用。PDGF 刺激导致特发性肺动脉高压患者 PASMCs 的生长速度明显高于正常对照 PASMCs,如(3)H-胸腺嘧啶掺入法所评估的那样。辛伐他汀(0.1 μmol/L)可显著抑制 PDGF 诱导的特发性肺动脉高压患者 PASMCs 的增殖,但在相同浓度下不抑制正常对照细胞的增殖。Western blot 分析显示,辛伐他汀可显著增加细胞周期抑制剂 p27 的表达。PDGF 可显著增加特发性肺动脉高压患者 PASMCs 的迁移距离,而辛伐他汀(1 μmol/L)可显著抑制 PDGF 诱导的迁移。免疫荧光染色显示,辛伐他汀(1 μmol/L)可抑制 Rho A 从细胞质向膜的易位和特发性肺动脉高压患者 PASMCs 中肌动蛋白纤维的紊乱。总之,辛伐他汀对特发性肺动脉高压患者 PASMCs 中不适当的 PDGF 信号具有抑制作用。

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