Qiao Huan, May James M
Department of Medicine, Vanderbilt University School of Medicine, Nashville, TN 37232-0475, USA.
Brain Res. 2008 May 7;1208:79-86. doi: 10.1016/j.brainres.2008.02.102. Epub 2008 Mar 18.
Ascorbic acid in its reduced form is not transported across the capillary endothelial cell blood-brain barrier. This is thought to be due to absence of the SVCT2, a specific transporter for ascorbate. To assess this directly we prepared primary cultures of mouse cortical microvascular endothelial cells. When still in the capillaries, these cells did not express the SVCT2 protein as assessed by immunocytochemistry and by immunoblotting. However, during several days in culture, they developed SVCT2 expression and showed ascorbate transport rates comparable to those in immortalized endothelial cell lines. SVCT2 expression was inversely proportional to cell density, was enhanced by culture at low physiologic plasma ascorbate concentrations, was inhibited by ascorbate concentrations expected in the brain interstitium, and was stimulated by cobalt ions. Expression of the SVCT2 was associated with ascorbate-dependent maturation and release of type IV collagen by the cells in culture. Although the SVCT2 is induced by culture of cortical capillary endothelial cells, its absence in vivo remains perplexing, given the need for intracellular ascorbate to facilitate type IV collagen maturation and release by endothelial cells.
还原形式的抗坏血酸不能穿过毛细血管内皮细胞血脑屏障。这被认为是由于缺乏SVCT2(一种抗坏血酸盐特异性转运体)。为了直接评估这一点,我们制备了小鼠皮质微血管内皮细胞原代培养物。通过免疫细胞化学和免疫印迹评估,当这些细胞仍在毛细血管中时,它们不表达SVCT2蛋白。然而,在培养的几天中,它们出现了SVCT2表达,并显示出与永生化内皮细胞系相当的抗坏血酸盐转运速率。SVCT2表达与细胞密度成反比,在低生理血浆抗坏血酸浓度下培养时增强,在脑间质预期的抗坏血酸浓度下受到抑制,并受到钴离子刺激。SVCT2的表达与培养细胞中抗坏血酸依赖性IV型胶原的成熟和释放有关。尽管SVCT2是由皮质毛细血管内皮细胞培养诱导产生的,但考虑到内皮细胞需要细胞内抗坏血酸来促进IV型胶原的成熟和释放,其在体内的缺失仍然令人困惑。