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血红素加氧酶-1/p21WAF1 介导过氧化物酶体增殖物激活受体-γ信号通路抑制大鼠肺动脉平滑肌细胞增殖。

Heme oxygenase-1/p21WAF1 mediates peroxisome proliferator-activated receptor-gamma signaling inhibition of proliferation of rat pulmonary artery smooth muscle cells.

机构信息

Department of Respiratory Medicine, The Second Affiliated Hospital of Medical College, Xi'an Jiaotong University, China.

出版信息

FEBS J. 2010 Mar;277(6):1543-50. doi: 10.1111/j.1742-4658.2010.07581.x. Epub 2010 Feb 13.

Abstract

Activation of peroxisome proliferator-activated receptor (PPAR)-gamma suppresses proliferation of rat pulmonary artery smooth muscle cells (PASMCs), and therefore ameliorates the development of pulmonary hypertension in animal models. However, the molecular mechanisms underlying this effect remain largely unknown. This study addressed this issue. The PPARgamma agonist rosiglitazone dose-dependently stimulated heme oxygenase (HO)-1 expression in PASMCs, 5 microm rosiglitazone inducing a 12.1-fold increase in the HO-1 protein level. Cells pre-exposed to rosiglitazone showed a dose-dependent reduction in proliferation in response to serotonin; this was abolished by pretransfection of cells with sequence-specific small interfering RNA against HO-1. In addition, rosiglitazone stimulated p21(WAF1) expression in PASMCs, a 2.34-fold increase in the p21(WAF1) protein level being achieved with 5 microm rosiglitazone; again, this effect was blocked by knockdown of HO-1. Like loss of HO-1, loss of p21(WAF1) through siRNA transfection also reversed the inhibitory effect of rosiglitazone on PASMC proliferation triggered by serotonin. Taken together, our findings suggest that activation of PPARgamma induces HO-1 expression, and that this in turn stimulates p21(WAF1) expression to suppress PASMC proliferation. Our study also indicates that rosiglitazone, a medicine widely used in the treatment of type 2 diabetes mellitus, has potential benefits for patients with pulmonary hypertension.

摘要

过氧化物酶体增殖物激活受体(PPAR)-γ 的激活可抑制大鼠肺动脉平滑肌细胞(PASMC)的增殖,从而改善动物模型中的肺动脉高压的发展。然而,这种作用的分子机制在很大程度上仍然未知。本研究解决了这个问题。PPARγ 激动剂罗格列酮可剂量依赖性地刺激 PASMC 中血红素加氧酶(HO)-1 的表达,5μM 罗格列酮诱导 HO-1 蛋白水平增加 12.1 倍。预先用罗格列酮处理的细胞对 5-羟色胺的增殖反应呈剂量依赖性降低;这一作用被针对 HO-1 的序列特异性小干扰 RNA 预先转染的细胞所消除。此外,罗格列酮可刺激 PASMC 中 p21(WAF1)的表达,5μM 罗格列酮可使 p21(WAF1)蛋白水平增加 2.34 倍;同样,这一作用也被 HO-1 的敲低所阻断。与 HO-1 的缺失一样,通过 siRNA 转染缺失 p21(WAF1)也可逆转罗格列酮对 5-羟色胺触发的 PASMC 增殖的抑制作用。总之,我们的研究结果表明,PPARγ 的激活诱导 HO-1 的表达,而这反过来又刺激 p21(WAF1)的表达以抑制 PASMC 的增殖。我们的研究还表明,罗格列酮,一种广泛用于治疗 2 型糖尿病的药物,可能对肺动脉高压患者有益。

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