Zhang Ling-yun, Ou Min, Huang You-zhang
Department of Cadre Respiration Medicine, Navy General Hospital of the PLA, Beijing 100048.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2011 Sep;31(9):1239-42.
To explore the effects of Yifei Huoxue Granule (YFHXG) on the proliferation and the transforming growth factor-beta (TGF-beta) activity of rat pulmonary artery smooth muscle cells (PASMCs) induced by platelet-derived growth factor BB (PDGF-BB).
Using tissue block adhering wall method, the primary rat PASMCs were cultured. PASMCs at the log phase growth were randomly divided into the control group, the PDGF-BB group, the PDGF-BB + high YFHXG group (at the final concentration of 7.5 mg/mL), the PDGF-BB + middle YFHXG group (at the final concentration of 1.5 mg/mL), and the PDGF-BB + low YFHXG group (at the final concentration of 0.3 mg/mL), respectively. MTT assay were employed to determine the cell proliferation rate of each group. Flow cytometric analyses were used to detect the cell cycle constituent ratio and the proliferation index (PI). In addition, TGF-beta protein's expression was determined by immunocytochemical assay (SP method).
Compared with the control group, the proliferation of PASMCs in the PDGF-BB group was obviously active (P<0.01). But when compared with the PDGF-BB group, along with the increased concentration of YFHXG, the growth of PASMCs was obviously inhibited, the cell ratio of G0/G1, phase obviously increased, the cell ratio of S + G2/M phase significantly decreased, and PI significantly decreased. Besides, the expression of TGF-beta protein decreased in a dose-dependent manner (P<0.05, P<0.01).
PDGF-BB could directly stimulate the proliferation of PASMCs. YFHXG had a significant inhibition on the proliferation of rat PASMCs induced by PDGF-BB and could regulate the expression of TGF-beta.
探讨益肺活血颗粒(YFHXG)对血小板衍生生长因子BB(PDGF - BB)诱导的大鼠肺动脉平滑肌细胞(PASMCs)增殖及转化生长因子β(TGF - β)活性的影响。
采用组织块贴壁法培养大鼠原代PASMCs。将处于对数生长期的PASMCs随机分为对照组、PDGF - BB组、PDGF - BB +高剂量益肺活血颗粒组(终浓度为7.5 mg/mL)、PDGF - BB +中剂量益肺活血颗粒组(终浓度为1.5 mg/mL)和PDGF - BB +低剂量益肺活血颗粒组(终浓度为0.3 mg/mL)。采用MTT法检测各组细胞增殖率。运用流式细胞术分析检测细胞周期组成比例及增殖指数(PI)。此外,采用免疫细胞化学检测法(SP法)测定TGF - β蛋白的表达。
与对照组相比,PDGF - BB组PASMCs增殖明显活跃(P<0.01)。但与PDGF - BB组相比,随着益肺活血颗粒浓度增加,PASMCs生长明显受抑制,G0/G1期细胞比例明显增加,S + G2/M期细胞比例显著降低,PI显著降低。此外,TGF - β蛋白表达呈剂量依赖性降低(P<0.05,P<0.01)。
PDGF - BB可直接刺激PASMCs增殖。益肺活血颗粒对PDGF - BB诱导的大鼠PASMCs增殖有显著抑制作用,并可调节TGF - β的表达。