Growth-related renal type IINa/Pi cotransporter

被引:209
作者
Segawa, H [1 ]
Kaneko, I [1 ]
Takahashi, A [1 ]
Kuwahata, M [1 ]
Ito, M [1 ]
Ohkido, I [1 ]
Tatsumi, S [1 ]
Miyamoto, K [1 ]
机构
[1] Univ Tokushima, Sch Med, Dept Nutr, Tokushima 7708503, Japan
关键词
D O I
10.1074/jbc.M200943200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Growth is critically dependent on the retention of a variety of nutrients. The kidney contributes to this positive external balance. In the present study, we isolated a cDNA from the human and rat kidney that encodes a growth-related Na+-dependent inorganic phosphate (P-i) cotransporter (type IIc). Microinjection of type IIc cRNA into Xenopus oocytes demonstrated sodium-dependent P-i cotransport activity. Affinity for P-i was 0.07 mm in 100 mm Na+. The transport activity was dependent on extracellular pH. In electrophysiological studies, type IIc Na/P-i cotransport was electroneutral, whereas type IIa was highly electrogenic. In Northern blotting analysis, the type IIc transcript was only expressed in the kidney and highly in weaning animals. In immunohistochemical analysis, the type IIc protein was shown to be localized at the apical membrane of the proximal tubular cells in superficial and midcortical nephrons of weaning rat kidney. Hybrid depletion experiments suggested that type IIc could function as a Na/P-i cotransporter in weaning animals, but its role is reduced in adults. The finding of the present study suggest that the type IIc is a growth-related renal Na/P-i cotransporter, which has a high affinity for P-i and is electroneutral.
引用
收藏
页码:19665 / 19672
页数:8
相关论文
共 28 条
[21]   Identification and functional characterization of a Na+-independent neutral amino acid transporter with broad substrate selectivity [J].
Segawa, H ;
Fukasawa, Y ;
Miyamoto, K ;
Takeda, E ;
Endou, H ;
Kanai, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (28) :19745-19751
[22]   Mechanism of renal phosphate retention during growth [J].
Silverstein, D ;
BaracNieto, M ;
Spitzer, A .
KIDNEY INTERNATIONAL, 1996, 49 (04) :1023-1026
[23]   A putative growth-related renal Na+-P-i cotransporter [J].
Silverstein, DM ;
BaracNieto, M ;
Murer, H ;
Spitzer, A ;
Zavilowitz, B .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 1997, 273 (03) :R928-R933
[24]   Cellular mechanisms of the age-related decrease in renal phosphate reabsorption [J].
Sorribas, V ;
Lotscher, M ;
Loffing, J ;
Biber, J ;
Kaissling, B ;
Murer, H ;
Levi, M .
KIDNEY INTERNATIONAL, 1996, 50 (03) :855-863
[25]   Ontogeny of renal phosphate transport and the process of growth [J].
Spitzer, A ;
Barac-Nieto, M .
PEDIATRIC NEPHROLOGY, 2001, 16 (09) :763-771
[26]   Identification of three isoforms for the Na+-dependent phosphate cotransporter (NaPi-2) in rat kidney [J].
Tatsumi, S ;
Miyamoto, K ;
Kouda, T ;
Motonaga, K ;
Katai, K ;
Ohkido, I ;
Morita, K ;
Segawa, H ;
Tani, Y ;
Yamamoto, H ;
Taketani, Y ;
Takeda, E .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (44) :28568-28575
[27]  
TAUFIQ A, 1997, AM J PHYSIOL, V272, pR134
[28]  
Traebert M, 1999, J AM SOC NEPHROL, V10, P1407