Lötscher M, Kaissling B, Biber J, Murer H, Levi M
Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas 75216, USA.
J Clin Invest. 1997 Mar 15;99(6):1302-12. doi: 10.1172/JCI119289.
Renal proximal tubular response to acute administration of a low Pi diet is characterized by a rapid adaptive increase in apical brush border membrane (BBM) Na-Pi cotransport activity and Na-Pi cotransporter protein abundance, independent of a change in Na-Pi cotransporter mRNA levels (Levi, M., M. Lötscher, V. Sorribas, M. Custer, M. Arar, B. Kaissling, H. Murer, and J. Biber. 1994. Am. J. Physiol. 267: F900-F908). The purposes of the present study were to determine if the acute adaptive response occurs independent of de novo protein synthesis, and if microtubules play a role in the rapid upregulation of the Na-Pi cotransporters at the apical BBM. We found that inhibition of transcription by actinomycin D and translation by cycloheximide did not prevent the rapid adaptive response. In addition, in spite of a 3.3-fold increase in apical BBM Na-Pi cotransporter protein abundance, there was no change in cortical homogenate Na-Pi cotransporter protein abundance. Pretreatment with colchicine, which resulted in almost complete disruption of the microtubular network, abolished the adaptive increases in BBM Na-Pi cotransport activity and Na-Pi cotransporter protein abundance. In contrast, colchicine had no effect on the rapid downregulation of Na-Pi cotransport in response to acute administration of a high Pi diet. We conclude that the rapid adaptive increase in renal proximal tubular apical BBM Na-Pi cotransport activity and Na-Pi cotransporter abundance is independent of de novo protein synthesis, and is mediated by microtubule-dependent translocation of presynthesized Na-Pi cotransporter protein to the apical BBM.
肾近端小管对急性给予低磷饮食的反应特点是,顶端刷状缘膜(BBM)的钠-磷共转运活性和钠-磷共转运蛋白丰度迅速适应性增加,且与钠-磷共转运蛋白mRNA水平的变化无关(Levi, M., M. Lötscher, V. Sorribas, M. Custer, M. Arar, B. Kaissling, H. Murer, and J. Biber. 1994. Am. J. Physiol. 267: F900-F908)。本研究的目的是确定这种急性适应性反应是否独立于从头合成蛋白质而发生,以及微管是否在顶端BBM处钠-磷共转运蛋白的快速上调中起作用。我们发现,放线菌素D抑制转录和环己酰亚胺抑制翻译并不能阻止这种快速适应性反应。此外,尽管顶端BBM钠-磷共转运蛋白丰度增加了3.3倍,但皮质匀浆中钠-磷共转运蛋白丰度没有变化。用秋水仙碱预处理导致微管网络几乎完全破坏,消除了BBM钠-磷共转运活性和钠-磷共转运蛋白丰度的适应性增加。相反,秋水仙碱对急性给予高磷饮食后钠-磷共转运的快速下调没有影响。我们得出结论,肾近端小管顶端BBM钠-磷共转运活性和钠-磷共转运蛋白丰度的快速适应性增加独立于从头合成蛋白质,并且是由预先合成的钠-磷共转运蛋白向顶端BBM的微管依赖性转位介导的。