He Bingyan, Deng Changsheng, Zhang Ming, Zou Dianding, Xu Min
Pediatrics Department of Zhongnan Hospital, Wuhan University, East-lake Road, Wuhan, Hubei Province 430071, PR China.
Leuk Res. 2007 Apr;31(4):507-14. doi: 10.1016/j.leukres.2006.06.015. Epub 2006 Aug 1.
To explore the effect of inhibition of Na(+)/H(+) exchanger isoform 1 (NHE1) on the expression of vascular endothelial growth factor (VEGF) mRNA and protein in human myeloid K562 cells. The expression of VEGFmRNA was detected by RT-PCR technique. The levels of VEGF protein were measured by Western blotting and immunocytochemistry assay. pHi values were measured with fluorescence spectrophotometer. The three RT-PCR products detected were VEGF121, VEGF165, and VEGF189, respectively. Treatment of K562 cells either with amiloride (an inhibitor of NHE1) or with 5-(N-ethyl-N-isopropyl)-amiloride (EIPA, a selective inhibitor of NHE1) resulted in significant decrease of VEGF mRNA and VEGF protein levels. Either amiloride or EIPA decreased intracellular pH (pHi) values in K562 cells. These data strongly suggested that the expression of VEGF mRNA and protein in K562 cells was inhibited accompanying its reduction in pHi value after targeted inhibition of NHE1.
探讨抑制钠氢交换体1(NHE1)对人髓系K562细胞中血管内皮生长因子(VEGF)mRNA和蛋白表达的影响。采用逆转录-聚合酶链反应(RT-PCR)技术检测VEGFmRNA的表达。通过蛋白质印迹法和免疫细胞化学分析法测定VEGF蛋白水平。用荧光分光光度计测量细胞内pH值(pHi)。检测到的三种RT-PCR产物分别为VEGF121、VEGF165和VEGF189。用氨氯吡咪(一种NHE1抑制剂)或5-(N-乙基-N-异丙基)-氨氯吡咪(EIPA,一种NHE1选择性抑制剂)处理K562细胞,导致VEGF mRNA和VEGF蛋白水平显著降低。氨氯吡咪或EIPA均可降低K562细胞内的pH值(pHi)。这些数据强烈表明靶向抑制NHE1后,K562细胞中VEGF mRNA和蛋白表达随pHi值降低而受到抑制