Department of Respiratory Medicine, the First Affiliated Hospital of Soochow University, Suzhou 215006, PR China.
Microvasc Res. 2013 Nov;90:144-9. doi: 10.1016/j.mvr.2013.07.012. Epub 2013 Aug 13.
Our previous study has demonstrated that a plasmid-based short hairpin RNA (shRNA) against cyclin D1 could attenuate the pulmonary artery smooth muscle cell (PASMC) proliferation and pulmonary vascular remodeling in smoking rats. In this report, we examined the efficiency of this shRNA plasmid in monocrotaline-induced pulmonary vascular remodeling. A single injection of monocrotaline induced pulmonary vascular remodeling and cyclin D1 over-expression in pulmonary vascular smooth muscle. The shRNA successfully suppressed the up-regulation of cyclin D1 in pulmonary vessels of monocrotaline-treated rats. Moreover, this shRNA decreased the percentage of muscularized vessels and the wall thickness of pulmonary vessels. So, we concluded that plasmid-based shRNA against cyclin D1 ameliorated pulmonary vascular remodeling in monocrotaline-treated rats. Cyclin D1 might be a potential target for the therapy of pulmonary vascular remodeling and pulmonary hypertension.
我们之前的研究表明,针对细胞周期蛋白 D1 的质粒短发夹 RNA(shRNA)可以减弱吸烟大鼠肺动脉平滑肌细胞 (PASMC)的增殖和肺血管重构。在本报告中,我们研究了这种 shRNA 质粒在野百合碱诱导的肺血管重构中的效率。单次注射野百合碱可诱导肺血管重构和肺血管平滑肌中环细胞周期蛋白 D1 的过度表达。shRNA 成功抑制了野百合碱处理大鼠肺血管中环细胞周期蛋白 D1 的上调。此外,这种 shRNA 降低了肌化血管的百分比和肺血管的壁厚度。因此,我们得出结论,针对细胞周期蛋白 D1 的质粒 shRNA 改善了野百合碱处理大鼠的肺血管重构。细胞周期蛋白 D1 可能是肺血管重构和肺动脉高压治疗的潜在靶点。