Tomi Masatoshi, Hosoya Ken-ichi
Faculty of Pharmaceutical Sciences, Toyama Medical and Pharmaceutical University, Sugitani, Toyama, Japan.
J Neurochem. 2004 Dec;91(5):1244-8. doi: 10.1111/j.1471-4159.2004.02842.x.
The purpose of the present study was to quantify transporter gene levels at the inner blood-retinal barrier (inner BRB) using a combination of magnetic isolation method for rat retinal vascular endothelial cells (RVEC) and real-time quantitative PCR analysis. The transcript levels of CD31, Tie-2, claudin-5, occludin, Jam-1, mdr1a, oatp2, and oatp14 in the RVEC fraction were more than 100-fold greater than those in the non-RVEC fraction, suggesting that these genes are predominantly expressed at the inner BRB. The transcript levels of GLUT1 and MCT1 in the RVEC fraction were the most abundant in the respective transporter family, suggesting that GLUT1 and MCT1 play a predominant role in d-glucose and monocarboxylate transport, respectively, at the inner BRB. In conclusion, application of magnetically isolated RVEC is able to determine transporter gene levels at the inner BRB thereby increasing our understanding of inner BRB functions at a molecular level.
本研究的目的是结合大鼠视网膜血管内皮细胞(RVEC)的磁分离方法和实时定量PCR分析,对血视网膜内屏障(内BRB)处的转运蛋白基因水平进行定量。RVEC组分中CD31、Tie-2、claudin-5、occludin、Jam-1、mdr1a、oatp2和oatp14的转录水平比非RVEC组分中的转录水平高100倍以上,这表明这些基因主要在内BRB处表达。RVEC组分中GLUT1和MCT1的转录水平在各自的转运蛋白家族中最为丰富,这表明GLUT1和MCT1分别在内BRB处的d-葡萄糖和单羧酸转运中起主要作用。总之,应用磁分离的RVEC能够确定内BRB处的转运蛋白基因水平,从而增进我们在分子水平上对血视网膜内屏障功能的理解。