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[缺氧大鼠中HIF-2α介导的FoxM1表达对肺动脉平滑肌细胞增殖的影响]

[Effect of HIF-2α mediated FoxM1 expression on proliferation of pulmonary artery smooth muscle cells in hypoxic rats].

作者信息

Zhu H, Zhu L M, Jiang Y L, Hu R C, Dai A G

机构信息

Department of Respiratory Medicine, Hunan Provincial People's Hospital (First Affiliated Hospital of Hunan Normal University), Changsha 410016, China.

Institute of Respiratory Diseases, Changsha Medical University, Changsha 410219, China.

出版信息

Zhonghua Yi Xue Za Zhi. 2019 Jan 8;99(2):129-134. doi: 10.3760/cma.j.issn.0376-2491.2019.02.011.

Abstract

To investigate the effect of hypoxia-inducible factor 2α (HIF-2α) gene on the expression of Forkhead box M1 (FoxM1) protein in the proliferation of hypoxic rat pulmonary artery smooth muscle cells (PASMC). HIF-2α overexpression lentiviral vector (LV-HIF-2α) and silencing RNA (siRNA) were constructed and transfected into rat PASMC under normoxia and hypoxia, respectively. The PASMC under normoxia were classified into normoxic control group, normoxia + LV-HIF-2α empty group, normoxia + LV-HIF-2α group; the PASMC under hypoxia were classified into hypoxic control group, hypoxia + siRNA-HIF-2α empty group, hypoxia + siRNA-HIF-2α group. The expression of HIF-2α and its downstream proteins FoxM1, cyclin D1 and Aurora A expressions were detected by Western blot. 5-Ethyny-2'-deoxyuridine (EdU) cell proliferation assay was used to evaluate the effect of overexpression and inhibition of HIF-2α expression on the proliferation of rat PASMC. The expression of HIF-2α in normoxia + LV-HIF-2α group was significantly higher than that in normoxic control group and normoxia+LV-HIF-2α empty group (0.17±0.02 vs 0.09±0.01 and 0.07±0.00), while the expression of HIF-2α in PASMC of hypoxia + siRNA-HIF-2α group was significantly lower than that of hypoxic control group and hypoxia + siRNA-HIF-2α empty group (0.28±0.01 vs 0.35±0.02 and 0.30±0.01) (all 0.05); the expression of FoxM1 protein, cyclinD1 and cell proliferation-related Aurora A protein in normoxia+LV-HIF-2α group were significantly higher than that in normoxic control group and normoxia+LV-HIF-2α empty group (0.40±0.03 vs 0.24±0.01 and 0.30±0.01, 0.22±0.02 vs 0.09±0.01 and 0.08±0.02, 0.29±0.02 vs 0.04±0.01 and 0.07±0.01, respectively) (all 0.05); the expressions of FoxM1 protein, cyclinD1 and Aurora A protein in hypoxia + siRNA-HIF-2α group were significantly lower than those in hypoxic control group and hypoxia + siRNA-HIF-2α empty group (0.23±0.01 vs 0.36±0.02 and 0.32±0.01, 0.15±0.01 vs 0.31±0.01 and 0.28±0.03, 0.14±0.02 vs 0.33±0.03 and 0.27±0.02, respectively) (all 0.05); the positive expression rate of EdU in the normoxic control group was significantly lower than that in the normoxia+LV-HIF-2α group [(30.77±2.43)% vs (55.56±3.01)%], while the hypoxic control group was significantly higher than the hypoxic+siRNA-HIF-2α group [(65.28±3.21)% vs (44.64±2.78)%] (both 0.05). HIF-2α up-regulates the expression of FoxM1 and promotes the proliferation of pulmonary artery smooth muscle cells in hypoxic rats.

摘要

探讨缺氧诱导因子2α(HIF-2α)基因对缺氧大鼠肺动脉平滑肌细胞(PASMC)增殖中叉头框M1(FoxM1)蛋白表达的影响。构建HIF-2α过表达慢病毒载体(LV-HIF-2α)和小干扰RNA(siRNA),分别在常氧和缺氧条件下转染大鼠PASMC。常氧下的PASMC分为常氧对照组、常氧+LV-HIF-2α空载体组、常氧+LV-HIF-2α组;缺氧下的PASMC分为缺氧对照组、缺氧+siRNA-HIF-2α空载体组、缺氧+siRNA-HIF-2α组。采用蛋白质免疫印迹法检测HIF-2α及其下游蛋白FoxM1、细胞周期蛋白D1和极光激酶A(Aurora A)的表达。采用5-乙炔基-2'-脱氧尿苷(EdU)细胞增殖检测法评估HIF-2α表达上调和抑制对大鼠PASMC增殖的影响。常氧+LV-HIF-2α组HIF-2α表达明显高于常氧对照组和常氧+LV-HIF-2α空载体组(0.17±0.02 vs 0.09±0.01和0.07±0.00),而缺氧+siRNA-HIF-2α组PASMC中HIF-2α表达明显低于缺氧对照组和缺氧+siRNA-HIF-2α空载体组(0.28±0.01 vs 0.35±0.02和0.30±0.01)(均P<0.05);常氧+LV-HIF-2α组FoxM1蛋白、细胞周期蛋白D1和细胞增殖相关的Aurora A蛋白表达明显高于常氧对照组和常氧+LV-HIF-2α空载体组(分别为0.40±0.03 vs 0.24±0.01和0.30±0.01、0.22±0.02 vs 0.09±0.01和0.08±0.02、0.29±0.02 vs 0.04±0.01和0.07±0.01)(均P<0.05);缺氧+siRNA-HIF-2α组FoxM1蛋白、细胞周期蛋白D1和Aurora A蛋白表达明显低于缺氧对照组和缺氧+siRNA-HIF-2α空载体组(分别为0.23±0.01 vs 0.36±0.02和0.32±0.01、0.15±0.01 vs 0.31±0.01和0.28±0.03、0.14±0.02 vs 0.33±0.03和0.27±0.02)(均P<0.05);常氧对照组EdU阳性表达率明显低于常氧+LV-HIF-2α组[(30.77±2.43)% vs(55.56±3.01)%],而缺氧对照组明显高于缺氧+siRNA-HIF-2α组[(65.28±3.21)% vs(44.64±2.78)%](均P<0.05)。HIF-2α上调FoxM1表达并促进缺氧大鼠肺动脉平滑肌细胞增殖。

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