吉林大学学报(医学版) ›› 2015, Vol. 41 ›› Issue (04): 747-750.doi: 10.13481/j.1671-587x.20150415

• 基础研究 • 上一篇    下一篇

小分子活性肽apelin在低氧诱导肺血管内皮细胞损伤中的表达及其意义

袁兆新1, 曾美纯2, 刘怡2, 陈然2, 范小芳2, 龚永生2, 孔晓霞2   

  1. 1. 长春医学高等专科学校护理系, 吉林 长春 130031;
    2. 温州医科大学基础医学院低氧医学研究所 机能学教研室, 浙江 温州 325035
  • 收稿日期:2015-03-13 发布日期:2015-08-01
  • 通讯作者: 孔晓霞,副教授,硕士研究生导师(Tel:0577-86699117,E-mail:kong_xx@hotmail.com) E-mail:kong_xx@hotmail.com
  • 作者简介:袁兆新(1974-),男,吉林省长春市人,副教授,医学博士,主要从事肿瘤病理生理学方面的研究。
  • 基金资助:

    国家自然科学基金资助课题(81200010);浙江省科技厅自然科学基金资助课题(LY12H01003)

Expression of apelin on PVECs injury induced by hypoxia and its significance

YUAN Zhaoxin1, ZHEN Meichun2, LIU Yi2, CHEN Ran2, FAN Xiaofang2, GONG Yongsheng2, KONG Xiaoxia2   

  1. 1. Nursing Faculty, Changchun Medical College, Changchun 130031, China;
    2. Department ofFunction, Institute of Hypoxia Medicine, School of Basic Medical Sciences, Wenzhou Medical University, Wenzhou 325035, China
  • Received:2015-03-13 Published:2015-08-01

摘要:

目的: 探讨apelin-APJ系统在低氧诱导肺血管内皮细胞(PVECs) 损伤中的表达变化,阐明小分子活性肽apelin对细胞增殖的影响。方法: 体外培养的大鼠PVECs 分为正常对照组、低氧6h组、低氧12h组、低氧24h组、低氧48h组、低氧24h加 apelin组和apelin组,MTT法检测各组细胞增殖率。体外培养的大鼠PVECs 分为正常对照组和低氧6h组、12h组及24h组,免疫荧光染色法检测细胞中apelin蛋白荧光表达,Western blotting法检测apelin-APJ系统蛋白表达水平。结果: 与正常对照组比较,低氧6、12 h组和apelin组细胞增殖率无明显变化(P>0.05),低氧24和48h组细胞增殖率明显降低 (P<0.05或P<0.01);与低氧24和48h组比较,低氧24h加apelin组细胞增殖率明显升高(P<0.05)。与正常对照组比较,低氧6h组细胞中apelin荧光表达强度无明显变化(P>0.05),低氧12和24h组细胞中apelin荧光表达强度明显降低(P<0.01)。与正常对照组比较,低氧6、12和24h组细胞中apelin蛋白表达水平明显下降(P<0.01),而APJ蛋白表达水平无明显变化(P>0.05)。结论: 低氧可能通过降低小分子活性肽apelin损伤内皮细胞,而外源性给予apelin在一定程度上能够保护低氧对肺血管内皮细胞的损伤作用。

关键词: 低氧, Apelin-APJ系统, 肺血管内皮细胞

Abstract:

Objective To investigate the changes of the expression of apelin-APJ system in the injury of pulmonary vascular endothelial cells (PVECs) under hypoxia conditions, and to clarify the role of apelin in the cell proliferation. Methods The in vitro cultured rat PVECs were divided into control group, hypoxia 6 h group, hypoxia 12 h group,hypoxia 24 h group,hypoxia 48 h group,hypoxia 24 h + apelin group and apelin group. The proliferation rates of PVECs in every group were detected by MTT assay. The in vitro cultured rat PVECs were divided into normal control group,hypoxia 6 h group,hypaxia 12 h group and hypoxia 24 h group.The expression of apelin in the cells were observed by immunofluorescence staining. The expression levels of apelin-APJ protein were measured by Western blotting method. Results Compared with normal control group, the proliferation rates of the PVECs in hypoxia 6 h,12h groups and apelin group had no change(P>0.05), but the proliferation rates of the PVECs in hypoxia 24 h and 48 h groups were decreased significantly(P<0.05 or P<0.01). Compared with normal control group, the immunofluorescence expression of apelin in the PVECs in hypoxia 6 h group had no obvious change(P>0.05), but the expression of apelin in the PVECs in hypoxia 12 h and 24 h groups were decreased (P<0.01). Compared with normal control group, the expression levels of apelin protein in the PVECs in hypoxia 6 h, 24 h and 48 h groups were decreased(P<0.01), but the protein expression of APJ in the PVECs had no significant changes(P>0.05). Conclusion Hypoxia may injury the PVECs through inhibiting the apelin expression, and exogenous apelin can protect the injure of PVECs induced by hypoxia.

Key words: hypoxia, apelin-APJ, pulmonary vascular endothelial cells

中图分类号: 

  • R363.2