基础医学与临床 ›› 2015, Vol. 35 ›› Issue (8): 1094-1099.

• 研究论文 • 上一篇    下一篇

CD44促进HUVEC增殖和黏附

石歆   

  1. 河南省中医学院第一附属医院
  • 收稿日期:2014-05-14 修回日期:2015-03-30 出版日期:2015-08-05 发布日期:2015-07-15
  • 通讯作者: 石歆 E-mail:shixin_tcm@163.com

CD44 promotes the proliferation and adhesion of human vascular endothelial cells

  • Received:2014-05-14 Revised:2015-03-30 Online:2015-08-05 Published:2015-07-15

摘要: 目的 研究CD44在血管内皮细胞增殖和粘附中的作用及机制。方法 采用pcDNA3.1载体上调人脐静脉血管内皮细胞(HUVEC)中CD44的表达。使用siRNA分别沉默HUVEC中Akt和血小板内皮细胞粘附因子(PECAM1)基因。MTT法测定细胞增殖,细胞计数法测定细胞粘附率,RT-PCR分析PECAM1的mRNA水平,Western blot分析蛋白Ki67、PECAM1以及Akt磷酸化水平。结果 CD44过表达显著促进了HUVEC的增殖(P<0.05),上调Ki67的表达并促进Akt的磷酸化(P<0.05);Akt siRNA显著降低了CD44诱导的细胞增殖(P<0.05)。CD44促进HUVEC细胞间粘附(P<0.05),上调PECAM1的mRNA和蛋白水平(P<0.05);PECAM1 siRNA降低CD44诱导的细胞粘附(P<0.05)。结论 CD44能够促进HUVEC的增殖和粘附,部分作用可能与上调PECAM1有关。

关键词: CD44, 血管内皮细胞, 细胞增殖, 细胞粘附

Abstract: Objective To study the effect and mechanism of CD44 in endothelial cell proliferation and adhesion. Methods The pcDNA3.1 vectors were constructed to upregulate the CD44 gene of Human umbilical vein endothelial cells (HUVEC); Akt siRNA and PECAM1 siRNA were used to knockdown the gene of Akt and PECAM1, respectively. Cell proliferation was measured by MTT assay, cell adhesion rate was measured by cell counting, PECAM1 mRNA levels were detected by RT-PCR, and Western blot was used to determine the protein levels of Ki67, PECAM1 and Akt phosphorylation. Results CD44 promoted HUVEC proliferation, increased Ki67 expression and promoted Akt phosphorylation (all P<0.05); while, Akt siRNA decreased the CD44-induced cell proliferation (P<0.05). Moreover, CD44 promote HUVEC adhesion (P<0.05), and increased the mRNA and protein levels of PECAM1 (all P<0.05); moreover, PECAM1 siRNA impaired CD44-induced cell adhesion. Conclusion CD44 promotes the proliferation of HUVEC cells by activating the Akt signaling pathway; CD44 promotes cell adhesion by increasing the mRNA and protein levels of PECAM1.

Key words: CD44, Vascular endothelial cells, cell proliferation, cell adhesion