Renal-Electrolyte Division, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261, USA.
Am J Physiol Renal Physiol. 2010 Jul;299(1):F167-77. doi: 10.1152/ajprenal.00162.2010. Epub 2010 May 12.
The metabolic sensor AMP-activated protein kinase (AMPK) regulates several transport proteins, potentially coupling transport activity to cellular stress and energy levels. The creatine transporter (CRT; SLC6A8) mediates creatine uptake into several cell types, including kidney epithelial cells, where it has been proposed that CRT is important for reclamation of filtered creatine, a process critical for total body creatine homeostasis. Creatine and phosphocreatine provide an intracellular, high-energy phosphate-buffering system essential for maintaining ATP supply in tissues with high energy demands. To test our hypothesis that CRT is regulated by AMPK in the kidney, we examined CRT and AMPK distribution in the kidney and the regulation of CRT by AMPK in cells. By immunofluorescence staining, we detected CRT at the apical pole in a polarized mouse S3 proximal tubule cell line and in native rat kidney proximal tubules, a distribution overlapping with AMPK. Two-electrode voltage-clamp (TEV) measurements of Na(+)-dependent creatine uptake into CRT-expressing Xenopus laevis oocytes demonstrated that AMPK inhibited CRT via a reduction in its Michaelis-Menten V(max) parameter. [(14)C]creatine uptake and apical surface biotinylation measurements in polarized S3 cells demonstrated parallel reductions in creatine influx and CRT apical membrane expression after AMPK activation with the AMP-mimetic compound 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside. In oocyte TEV experiments, rapamycin and the AMPK activator 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranosyl 5'-monophosphate (ZMP) inhibited CRT currents, but there was no additive inhibition of CRT by ZMP, suggesting that AMPK may inhibit CRT indirectly via the mammalian target of rapamycin pathway. We conclude that AMPK inhibits apical membrane CRT expression in kidney proximal tubule cells, which could be important in reducing cellular energy expenditure and unnecessary creatine reabsorption under conditions of local and whole body metabolic stress.
代谢传感器 AMP 激活的蛋白激酶(AMPK)调节几种转运蛋白,可能将转运活性与细胞应激和能量水平联系起来。肌酸转运蛋白(CRT;SLC6A8)介导肌酸进入几种细胞类型的摄取,包括肾上皮细胞,在这些细胞中,CRT 被认为对过滤的肌酸的再摄取很重要,这是全身肌酸动态平衡的关键过程。肌酸和磷酸肌酸提供细胞内高能磷酸盐缓冲系统,对于维持高能量需求组织中的 ATP 供应至关重要。为了检验我们的假设,即 CRT 在肾脏中受 AMPK 调节,我们检查了肾脏中 CRT 和 AMPK 的分布以及 AMPK 对 CRT 的调节。通过免疫荧光染色,我们在极化的鼠 S3 近端肾小管细胞系和原代大鼠肾脏近端小管中检测到 CRT 在顶端极,其分布与 AMPK 重叠。用双电极电压钳(TEV)测量表达 CRT 的非洲爪蟾卵母细胞中 Na(+)-依赖性肌酸摄取表明,AMPK 通过降低其米氏常数-V(max)参数来抑制 CRT。在极化的 S3 细胞中进行 [(14)C]肌酸摄取和顶端表面生物素化测量表明,在 AMPK 激活后,用 AMP 模拟化合物 5-氨基咪唑-4-甲酰胺-1-β-D-核糖呋喃糖苷(5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside),肌酸内流和 CRT 顶端膜表达均平行减少。在卵母细胞 TEV 实验中,雷帕霉素和 AMPK 激活剂 5-氨基咪唑-4-甲酰胺-1-β-D-核糖呋喃糖苷 5'-单磷酸(ZMP)抑制 CRT 电流,但 ZMP 对 CRT 没有附加抑制作用,表明 AMPK 可能通过哺乳动物雷帕霉素靶蛋白途径间接抑制 CRT。我们得出结论,AMPK 抑制肾脏近端小管细胞中顶端膜 CRT 的表达,这在局部和全身代谢应激条件下减少细胞能量消耗和不必要的肌酸重吸收可能很重要。