Proximal tubule Na+/H+ exchanger activity in adult NHE8-/-, NHE3-/-, and NHE3-/-/NHE8-/- mice

被引:23
作者
Baum, Michel [1 ,2 ]
Twombley, Katherine [1 ]
Gattineni, Jyothsna [1 ]
Joseph, Catherine [1 ]
Wang, Lin [1 ]
Zhang, Qiuyu [1 ]
Dwarakanath, Vangipuram [1 ]
Moe, Orson W. [2 ,3 ,4 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Pediat, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Dept Internal Med, Dallas, TX 75390 USA
[3] Univ Texas SW Med Ctr Dallas, Dept Physiol, Dallas, TX 75390 USA
[4] Univ Texas SW Med Ctr Dallas, Charles & Jane Pak Ctr Mineral Metab & Clin Res, Dallas, TX 75390 USA
基金
美国国家卫生研究院;
关键词
sodium/hydrogen exchanger; proximal tubule; development; acidosis; RENAL BRUSH-BORDER; CONVOLUTED TUBULE; METABOLIC-ACIDOSIS; BICARBONATE ABSORPTION; NULL MICE; NHE3; SODIUM; ACIDIFICATION; EXPRESSION; ISOFORM;
D O I
10.1152/ajprenal.00415.2012
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Baum M, Twombley K, Gattineni J, Joseph C, Wang L, Zhang Q, Dwarakanath V, Moe OW. Proximal tubule Na+/H+ exchanger activity in adult NHE8(-/-), NHE3(-/-), and NHE3(-/-)/NHE8(-/-) mice. Am J Physiol Renal Physiol 303: F1495-F1502, 2012. First published October 10, 2012; doi: 10.1152/ajprenal.00415.2012.-NHE3 is the predominant Na+/H+ exchanger on the brush-border membrane (BBM) of the proximal tubule in adults. However, NHE3 null mice still have significant renal BBM Na+/H+ activity. NHE8 has been localized to the BBM of proximal tubules and is more highly expressed in neonates than adult animals. The relative role of NHE8 in adult renal H+ transport is unclear. This study examined whether there was compensation by NHE8 in NHE3(-/-) mice and by NHE3 in NHE8(-/-) mice. NHE3(-/-) mice had significant metabolic acidosis, and renal BBM NHE8 protein abundance was greater in NHE3(-/-) mice than control mice, indicating that there may be compensation by NHE8 in NHE3(-/-) mice. NHE8(-/-) mice had serum bicarbonate levels and pH that were not different from controls. NHE3 protein expression on the BBM was greater in NHE8(-/-) mice than in wild-type mice, indicating that there may be compensation by NHE3 in NHE8(-/-) mice. Both BBM NHE3 and NHE8 protein abundance increased in response to acidosis. Blood pressure and Na+/H+ exchanger activity were comparable in NHE8(-/-) mice to that of controls, but both were significantly lower in NHE3(-/-) mice compared with control mice. Compared with NHE3(-/-) mice, NHE3(-/-)/NHE8(-/-) mice had lower blood pressures. While serum bicarbonate was comparable in NHE3(-/-) mice and NHE3(-/-)/NHE8(-/-) mice, proximal tubule Na+/H+ exchange activity was less in NHE3(-/-)/NHE8(-/-) mice compared with NHE3(-/-) mice. In conclusion, NHE3 is the predominant Na+/H+ exchanger in adult mice. NHE8 may play a compensatory role in renal acidification and blood pressure regulation in NHE3(-/-) mice.
引用
收藏
页码:F1495 / F1502
页数:8
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