Mailleau C, Capeau J, Brahimi-Horn M C
Institut National de la Santé et de la Recherche Médicale U. 402, Faculté de Médecine Saint-Antoine, Paris, France.
J Cell Physiol. 1998 Sep;176(3):472-81. doi: 10.1002/(SICI)1097-4652(199809)176:3<472::AID-JCP4>3.0.CO;2-L.
Both the Na+-dependent glucose cotransporter (SGLT1) and the cystic fibrosis transmembrane conductance regulator (CFTR) modulate Na+ and fluid movement, although in opposite directions. Yet few studies have investigated a possible interrelationship between these two transporters. By using the Caco-2 human colon carcinoma cell line, we confirmed that the activities of these transporters increased with spontaneous differentiation to the enterocytic phenotype. We showed that SGLT1 was positively regulated by Cl- and that optimal activity of CFTR was dependent on the presence of glucose. We also demonstrated that inhibition of CFTR by glibenclamide or diphenylamine-2-carboxylate did not modify the activity of SGLT1 and inhibition of SGLT1 by phlorizin did not modify the activity of CFTR, although it resulted in inhibition of glycoconjugate synthesis. These results point to positive substrate-cross regulation of SGLT1 and CFTR and suggest that NaCl and glucose are important for not only Na+ absorption and fluid movement, but also for cAMP-dependent Cl- efflux, and glycoconjugate synthesis, functions that are known to be anomalous in cystic fibrosis.
钠依赖性葡萄糖共转运蛋白(SGLT1)和囊性纤维化跨膜传导调节因子(CFTR)均可调节钠和液体的移动,尽管二者作用方向相反。然而,很少有研究探讨这两种转运蛋白之间可能存在的相互关系。通过使用Caco-2人结肠癌细胞系,我们证实这些转运蛋白的活性随着向肠细胞表型的自发分化而增加。我们发现SGLT1受氯离子正向调节,且CFTR的最佳活性依赖于葡萄糖的存在。我们还证明,格列本脲或二苯胺-2-羧酸盐对CFTR的抑制不会改变SGLT1的活性,而根皮苷对SGLT1的抑制不会改变CFTR的活性,尽管这会导致糖缀合物合成受到抑制。这些结果表明SGLT1和CFTR存在正向底物交叉调节,并提示氯化钠和葡萄糖不仅对钠吸收和液体移动很重要,而且对环磷酸腺苷依赖性氯离子外流以及糖缀合物合成也很重要,而这些功能在囊性纤维化中已知是异常的。