Immunolocalization of electrogenic sodium-bicarbonate cotransporters pNBC1 and kNBC1 in the rat eye

被引:78
作者
Bok, D
Schibler, MJ
Pushkin, A
Sassani, P
Abuladze, N
Naser, Z
Kurtz, I
机构
[1] Univ Calif Los Angeles, Sch Med, Div Nephrol, Ctr Hlth Sci, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Sch Med, Jules Stein Eye Inst, Dept Neurobiol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Sch Med, Inst Brain Res, Los Angeles, CA 90095 USA
[4] Innovex Biosci, Richmond, CA 94805 USA
关键词
bicarbonate; sodium; transport; eyes; cornea; ciliary body; retina;
D O I
10.1152/ajprenal.2001.281.5.F920
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
The human NBC1 gene encodes two electrogenic sodium-bicarbonate co-transport proteins, pNBC1 and kNBC1, which are candidate proteins for mediating electrogenic sodium-bicarbonate co-transport in ocular cells. Mutations in the coding region of the human NBC1 gene in exons common to both pNBC1 and kNBC1 result in a syndrome with a severe ocular and renal phenotype (blindness, band keratopathy, glaucoma, cataracts, and proximal renal tubular acidosis). In the present study, we determined the pattern of electrogenic sodium-bicarbonate co-transporter protein expression in rat eye. For this purpose, pNBC1- and kNBC1-specific antibodies were generated and used to detect these NBC1 protein variants by immunoblotting and immunocytochemistry. pNBC1 is expressed in cornea, conjunctiva, lens, ciliary body, and retina, whereas the expression of kNBC1 is restricted to the conjunctiva. These results provide the first evidence for extrarenal kNBC1 protein expression. The data in this study will serve as a basis for understanding the molecular mechanisms responsible for abnormalities in ocular electrogenic sodium-bicarbonate cotransport in patients with mutations in the NBC1 gene.
引用
收藏
页码:F920 / F935
页数:16
相关论文
共 70 条
[11]   LIGHT-EVOKED CHANGES IN EXTRACELLULAR PH IN FROG RETINA [J].
BORGULA, GA ;
KARWOSKI, CJ ;
STEINBERG, RH .
VISION RESEARCH, 1989, 29 (09) :1069-1077
[12]   Cloning and functional expression of a human kidney Na+:HCO3- cotransporter [J].
Burnham, CE ;
Amlal, H ;
Wang, ZH ;
Shull, GE ;
Soleimani, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (31) :19111-19114
[13]   SHORT-CIRCUIT CURRENT AND ACTIVE NA TRANSPORT ACROSS ISOLATED LENS OF TOAD [J].
CANDIA, OA ;
BENTLEY, PJ ;
MILLS, CD .
AMERICAN JOURNAL OF PHYSIOLOGY, 1971, 220 (02) :558-&
[14]   Characterization of α-crystallin-plasma membrane binding [J].
Cobb, BA ;
Petrash, JM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (09) :6664-6672
[15]  
EDELMAN JL, 1991, INVEST OPHTH VIS SCI, V32, P3033
[17]   ENDOGENOUS H+ MODULATION OF NMDA RECEPTOR-MEDIATED EPSCS REVEALED BY CARBONIC-ANHYDRASE INHIBITION IN RAT HIPPOCAMPUS [J].
GOTTFRIED, JA ;
CHESLER, M .
JOURNAL OF PHYSIOLOGY-LONDON, 1994, 478 (03) :373-378
[18]   The stoichiometry of the electrogenic sodium bicarbonate cotransporter NBC1 is cell-type dependent [J].
Gross, E ;
Hawkins, K ;
Abuladze, N ;
Pushkin, A ;
Cotton, CU ;
Hopfer, U ;
Kurtz, I .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 531 (03) :597-603
[19]   The stoichiometry of the electrogenic sodium bicarbonate cotransporter pNBC1 in mouse pancreatic duct cells is 2 HCO3-:1 Na+ [J].
Gross, E ;
Abuladze, N ;
Pushkin, A ;
Kurtz, I ;
Cotton, CU .
JOURNAL OF PHYSIOLOGY-LONDON, 2001, 531 (02) :375-382
[20]   Aquaporins in complex tissues: distribution of aquaporins 1-5 in human and rat eye [J].
Hamann, S ;
Zeuthen, T ;
La Cour, M ;
Ottersen, OP ;
Agre, P ;
Nielsen, S .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1998, 274 (05) :C1332-C1345