The molecular mechanism and potential dependence of the Na+/glucose cotransporter

被引:11
作者
Bennett, E [1 ]
Kimmich, GA [1 ]
机构
[1] UNIV ROCHESTER,SCH MED & DENT,DEPT BIOPHYS & BIOCHEM,ROCHESTER,NY 14642
关键词
D O I
10.1016/S0006-3495(96)79730-8
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Activity of the Na+/glucose cotransporter endogenously expressed in LLC-PK1 cells was measured using whole cell recording techniques under three different sodium concentration conditions: 1) externally saturating, zero trans; 2) 40 mM external, zero trans; and 3) externally saturating, 50 mM trans. Activity of the transporter with increasing concentrations of sugar was measured for each set of conditions, from which the maximal current for saturating sugar, I-m was determined. The I-m measured shows substantial potential dependence for each set of conditions. The absolute I-m and the relative potential dependence of I-m compared among the various solute conditions were used to identify which loci in the transport cycle are responsible for potential-dependent changes in function. The experimental data were compared with the predicted I-m values calculated from an eight-state, sequential, reversible model of a transport reaction kinetic scheme. Predictions derived from assignment of rate limitation and/or potential dependence to each of the 10 transitions in the transport pathway were derived and compared with the measured data. Most putative models were dismissed because of lack of agreement with the measured data, indicating that several steps along the transport pathway are not rate limiting and/or not potential dependent. Only two models were found that can completely account for the measured data. In one case, translocation of the free carrier must be rate limiting, and both extracellular sodium-binding events as well as translocation of both free and fully loaded carrier forms must be potential-dependent transitions. In the second case, translocation of the free carrier and dissociation of the first sodium to be released intracellularly must be equivalently rate limiting. In this case only the two translocation events are required to be potential dependent. The two external sodium-binding events might still be potential dependent, but this is not required to fit the data. Previous reports suggest that the first model is correct; however, no direct experimental data compel us to dismiss the second option as a feasible model.
引用
收藏
页码:1676 / 1688
页数:13
相关论文
共 29 条
[21]   THE MECHANISTIC NATURE OF THE MEMBRANE-POTENTIAL DEPENDENCE OF SODIUM-SUGAR COTRANSPORT IN SMALL-INTESTINE [J].
RESTREPO, D ;
KIMMICH, GA .
JOURNAL OF MEMBRANE BIOLOGY, 1985, 87 (02) :159-172
[22]   KINETIC-ANALYSIS OF MECHANISM OF INTESTINAL NA+-DEPENDENT SUGAR-TRANSPORT [J].
RESTREPO, D ;
KIMMICH, GA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1985, 248 (05) :C498-C509
[23]   PHLORIZIN BINDING TO ISOLATED ENTEROCYTES - MEMBRANE-POTENTIAL AND SODIUM DEPENDENCE [J].
RESTREPO, D ;
KIMMICH, GA .
JOURNAL OF MEMBRANE BIOLOGY, 1986, 89 (03) :269-280
[24]   ELECTRO-PHYSIOLOGICAL ANALYSIS OF RAT RENAL SUGAR AND AMINO-ACID-TRANSPORT .5. ACIDIC AMINO-ACIDS [J].
SAMARZIJA, I ;
FROMTER, E .
PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 1982, 393 (03) :215-221
[25]  
SANDERS D, 1984, J MEMBRANE BIOL, V77, P123
[26]  
Segel I.H., 1975, Enzyme kinetics
[27]   WHOLE CELL RECORDING OF SUGAR-INDUCED CURRENTS IN LLC-PK1 CELLS [J].
SMITHMAXWELL, C ;
BENNETT, E ;
RANDLES, J ;
KIMMICH, GA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1990, 258 (02) :C234-C242
[28]   INTESTINAL NA+ GLUCOSE COTRANSPORTER EXPRESSED IN XENOPUS-OOCYTES IS ELECTROGENIC [J].
UMBACH, JA ;
COADY, MJ ;
WRIGHT, EM .
BIOPHYSICAL JOURNAL, 1990, 57 (06) :1217-1224
[29]  
Woodbury JW., 1971, CHEM DYNAMICS PAPERS, P601