Lee C W, Cheeseman C I, Jarvis S M
Department of Physiology, University of Alberta, Edmonton, Canada.
Am J Physiol. 1990 May;258(5 Pt 2):F1203-10. doi: 10.1152/ajprenal.1990.258.5.F1203.
The uptake of uridine into rat renal brush-border membrane vesicles is mediated by Na(+)- and K(+)-dependent concentrative transport processes. At a 100 mM extravesicular cation concentration the apparent Km values were 9.7 +/- 4.2 and 28 +/- 5 microM, and Vmax values were 28 +/- 4 and 7 +/- 1 pmol.mg protein-1.s-1 for the Na(+)- and K(+)-dependent systems, respectively. Uracil, D-ribose, and D-glucose failed to inhibit the uptake processes, indicating that these carriers are specific for nucleosides. Other purines and pyrimidines inhibited uridine uptake competitively, although these two transport systems seem to favor adenosine and pyrimidines as permeants. Evidence is also given that transport is rheogenic, involving a net transfer of positive charge. The Na+:uridine and K+:uridine coupling stoichiometry was found to be 1:1 and 3:2, respectively. Both systems can also be driven by an anion gradient with apparent NO3- affinity (KNO3-) values of 42 +/- 13 and 163 +/- 54 mM for Na(+)- and K(+)-dependent systems, respectively.
尿苷进入大鼠肾刷状缘膜囊泡是由Na⁺和K⁺依赖性的浓缩转运过程介导的。在细胞外阳离子浓度为100 mM时,Na⁺依赖性和K⁺依赖性系统的表观Km值分别为9.7±4.2和28±5 μM,Vmax值分别为28±4和7±1 pmol·mg蛋白⁻¹·s⁻¹。尿嘧啶、D-核糖和D-葡萄糖不能抑制摄取过程,表明这些载体对核苷具有特异性。其他嘌呤和嘧啶竞争性抑制尿苷摄取,尽管这两种转运系统似乎更倾向于腺苷和嘧啶作为渗透物。也有证据表明转运是生电的,涉及正电荷的净转移。发现Na⁺:尿苷和K⁺:尿苷的偶联化学计量分别为1:1和3:2。这两种系统也都可以由阴离子梯度驱动,Na⁺依赖性和K⁺依赖性系统的表观NO₃⁻亲和力(KNO₃⁻)值分别为42±13和163±54 mM。