Sullivan L P, Grantham J A, Rome L, Wallace D, Grantham J J
Department of Physiology, University of Kansas School of Medicine, Kansas City 66103.
Am J Physiol. 1990 Jan;258(1 Pt 2):F46-51. doi: 10.1152/ajprenal.1990.258.1.F46.
An epifluorometric method was used to quantify the bidirectional fluxes of fluorescein across the basolateral surfaces of nonperfused rabbit tubule segments in vitro. Proximal S2 segments, but not cortical collecting tubules or cortical thick ascending limbs, accumulated fluorescein to levels in cytoplasm over 100-fold greater than in the external medium. The rate of intracellular fluorescein accumulation was dependent on the concentration of the ligand in the external bath. The apparent Km was 10 microM and the Vmax was 623 x 10(-6) mol.min-1.l-1. Probenecid and ouabain inhibited fluorescein accumulation. We conclude that fluorescein is transported into the cytoplasm of proximal tubules by basolateral mechanisms that share features in common with the classical organic anion system. This fluorescent compound offers some unique advantages for the study of the organic anion transport system in intact cells.
采用落射荧光测定法对体外未灌注兔肾小管节段基底外侧表面荧光素的双向通量进行定量。近端S2节段而非皮质集合管或皮质厚升支将荧光素积聚于细胞质中,其水平比外部介质中高100倍以上。细胞内荧光素的积聚速率取决于外部浴中配体的浓度。表观Km为10微摩尔,Vmax为623×10⁻⁶摩尔·分钟⁻¹·升⁻¹。丙磺舒和哇巴因抑制荧光素的积聚。我们得出结论,荧光素通过基底外侧机制转运至近端小管的细胞质中,这些机制与经典有机阴离子系统具有共同特征。这种荧光化合物为完整细胞中有机阴离子转运系统的研究提供了一些独特的优势。