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大鼠肾内体组分中的钠依赖性磷酸盐转运

Sodium-dependent phosphate transport in a rat kidney endosomal fraction.

作者信息

Abraham M I, Burckhardt G, Kempson S A

机构信息

Department of Physiology and Biophysics, Indiana University School of Medicine, Indianapolis.

出版信息

Kidney Int. 1992 Nov;42(5):1070-8. doi: 10.1038/ki.1992.389.

Abstract

An endosome-enriched fraction was prepared from rat kidney cortex by a standard procedure employing centrifugation on a Percoll gradient. This fraction showed time-dependent accumulation of inorganic phosphate (Pi) which was stimulated two- to threefold during the initial phase by an inwardly directed Na+ gradient. Na+ gradient-dependent Pi accumulation decreased with increasing medium osmolality and Pi binding accounted for only 16% of the total accumulation at two minutes. Like the Pi transporter in the brush border membrane (BBM), the Na+ gradient-dependent Pi uptake (but not the Na(+)-independent component) by the endosomal fraction was stimulated by intravesicular Pi and by an outwardly directed proton gradient, and was inhibited by extravesicular arsenate. Unlike the Pi transporter in BBM, the endosomal Pi transporter was not changed by acidic pH under non-gradient conditions. Activation of the endosomal proton pump by extravesicular ATP, leading to acidification of the vesicle interior, was accompanied by stimulation of endosomal Na+ gradient-dependent Pi transport. Inhibition of the proton pump by deletion of chloride or addition of N-ethylmaleimide abolished the stimulation of Pi uptake by ATP. The data indicate that the Na(+)-dependent Pi transporter in renal endosomal fractions is an intrinsic endosomal component. It remains to be determined if the endosomal Pi transporter plays a role in regulation of renal Pi transport.

摘要

通过在Percoll梯度上离心的标准程序,从大鼠肾皮质制备了富含内体的组分。该组分显示出无机磷酸盐(Pi)的时间依赖性积累,在初始阶段,内向的Na +梯度可将其刺激两到三倍。随着培养基渗透压的增加,Na +梯度依赖性Pi积累减少,并且在两分钟时Pi结合仅占总积累的16%。与刷状缘膜(BBM)中的Pi转运蛋白一样,内体组分对Na +梯度依赖性Pi的摄取(而非不依赖Na +的组分)受到囊泡内Pi和外向质子梯度的刺激,并受到囊泡外砷酸盐的抑制。与BBM中的Pi转运蛋白不同,在非梯度条件下,酸性pH不会改变内体Pi转运蛋白。囊泡外ATP激活内体质子泵,导致囊泡内部酸化,同时刺激内体Na +梯度依赖性Pi转运。通过缺失氯离子或添加N-乙基马来酰亚胺抑制质子泵消除了ATP对Pi摄取的刺激。数据表明,肾内体组分中依赖Na +的Pi转运蛋白是内体的固有成分。内体Pi转运蛋白是否在肾Pi转运调节中起作用还有待确定。

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