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大鼠近端小管中NHE8的个体发生。

Ontogeny of NHE8 in the rat proximal tubule.

作者信息

Becker Amy M, Zhang Jianning, Goyal Sunita, Dwarakanath Vangipuram, Aronson Peter S, Moe Orson W, Baum Michel

机构信息

Dept. of Pediatrics, University of Texas Southwestern Medical Center, 5323 Harry Hines Blvd., Dallas, TX 75390-9063, USA.

出版信息

Am J Physiol Renal Physiol. 2007 Jul;293(1):F255-61. doi: 10.1152/ajprenal.00400.2006. Epub 2007 Apr 11.

Abstract

Proximal tubule bicarbonate reabsorption is primarily mediated via the Na(+)/H(+) exchanger, identified as NHE3 in adults. Previous studies have demonstrated a maturational increase in rat proximal tubule NHE3 expression, with a paucity of NHE3 expression in neonates, despite significant Na(+)-dependent proton secretion. Recently, a novel Na(+)/H(+) antiporter (NHE8) was identified and found to be expressed on the apical membrane of the proximal tubule. To determine whether NHE8 may be the antiporter responsible for proton secretion in neonates, the present study characterized the developmental expression of NHE8 in rat proximal tubules. RNA blots and real-time RT-PCR demonstrated no developmental difference in the mRNA of renal NHE8. Immunoblots, however, demonstrated peak protein abundance of NHE8 in brush border membrane vesicles of 7- and 14-day-old compared with adult rats. In contrast, the level of NHE8 expression in total cortical membrane protein was higher in adults than in neonates. Immunohistochemistry confirmed the presence of NHE8 on the apical membrane of the proximal tubules of neonatal and adult rats. These data demonstrate that NHE8 does undergo maturational changes on the apical membrane of the rat proximal tubule and may account for the Na(+)-dependent proton flux in neonatal proximal tubules.

摘要

近端小管碳酸氢盐重吸收主要通过钠氢交换体介导,在成人中该交换体为NHE3。既往研究表明,大鼠近端小管NHE3表达随发育成熟而增加,尽管新生大鼠存在显著的钠依赖型质子分泌,但NHE3在新生大鼠中的表达较少。最近,一种新型钠氢反向转运体(NHE8)被鉴定出来,并发现其表达于近端小管的顶端膜上。为了确定NHE8是否可能是新生大鼠中负责质子分泌的反向转运体,本研究对大鼠近端小管中NHE8的发育表达进行了表征。RNA印迹和实时RT-PCR显示,肾脏NHE8的mRNA在发育过程中无差异。然而,免疫印迹显示,与成年大鼠相比,7日龄和14日龄大鼠刷状缘膜囊泡中NHE8的蛋白丰度达到峰值。相反,成年大鼠皮质总膜蛋白中NHE8的表达水平高于新生大鼠。免疫组织化学证实,NHE8存在于新生大鼠和成年大鼠近端小管的顶端膜上。这些数据表明,NHE8在大鼠近端小管顶端膜上确实经历了成熟变化,可能是新生大鼠近端小管中钠依赖型质子通量的原因。

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