Changes in membrane and surface potential explain the opposite effects of low ionic strength on the two lysine transporters of human erythrocytes

被引:13
作者
Deves, R
Angelo, S
机构
[1] Department of Physiology, Faculty of Medicine, University of Chile, Santiago
[2] Dept. de Fisiología, Facultad de Medicina, U. de Chile, Casilla 70005
关键词
D O I
10.1074/jbc.271.50.32034
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
The sucrose-induced stimulation of lysine influx in human erythrocytes has been attributed to the removal of a competitive inhibition exerted by Na+ on system y(+) (Young, J. D., Fincham, D. A., and Harvey, C. M, (1991) Biochim Biophys. Acta 1070, 111-118). We have reexamined this phenomenon separating the contribution of the two cationic amino acid transporters present in these cells (system y(+) and system y(+)L). NaCl replacement with sucrose increased influx through system y(+)L, but decreased influx through system y(+). We conclude that 1) the inhibition of system y(+) is a response to the membrane depolarization that results from chloride removal, and 2) the stimulation of system y(+)L is due to the enhancement of the negative surface potential. Consistently, lysine influx through system y(+)L (in sucrose medium) was reduced by Na+, K+, Li+, and choline (K-0.5 = 25-34 mM), the effect reaching a maximum at 35-40% of the original flux. Divalent cations (Ca2+ and Mg2+) were also inhibitory, but lower concentrations were required (K-0.5 1.1-1.8 mM). The finding that sucrose stimulates uptake through changes in the surface potential explains similar effects observed in other cells with various cationic substrates.
引用
收藏
页码:32034 / 32039
页数:6
相关论文
共 19 条
[11]   VOLTAGE-DEPENDENCE OF FACILITATED ARGININE FLUX MEDIATED BY THE SYSTEM Y+ BASIC-AMINO-ACID TRANSPORTER [J].
KAVANAUGH, MP .
BIOCHEMISTRY, 1993, 32 (22) :5781-5785
[12]  
MCLAUGHLIN S, 1977, CURR TOP MEMBR TRANS, V9, P71
[13]  
RINK TJ, 1982, RED CELL MEMBRANES M, P321
[14]   INFLUENCE OF SURFACE CHARGE ON KINETICS OF ION-TRANSLOCATION ACROSS BIOLOGICAL-MEMBRANES [J].
THEUVENET, APR ;
BORSTPAUWELS, GWFH .
JOURNAL OF THEORETICAL BIOLOGY, 1976, 57 (02) :313-329
[15]  
THOMAS EL, 1971, J BIOL CHEM, V246, P1677
[16]   THE CATION RECEPTOR SUBSITE OF THE CHOLINE TRANSPORTER IN PREIMPLANTATION MOUSE CONCEPTUSES RESEMBLES A CATION RECEPTOR SUBSITE OF SEVERAL AMINO-ACID TRANSPORTERS [J].
VANWINKLE, LJ ;
CAMPIONE, AL ;
MANN, DF ;
WASSERLAUF, HG .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1146 (01) :38-44
[17]   INHIBITION OF TRANSPORT-SYSTEM BO,+ IN BLASTOCYSTS BY INORGANIC AND ORGANIC CATIONS YIELDS INSIGHT INTO THE STRUCTURE OF ITS AMINO-ACID RECEPTOR-SITE [J].
VANWINKLE, LJ ;
CAMPIONE, AL ;
GORMAN, JM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1990, 1025 (02) :215-224
[18]   ENDOGENOUS AMINO-ACID-TRANSPORT SYSTEMS AND EXPRESSION OF MAMMALIAN AMINO-ACID-TRANSPORT PROTEINS IN XENOPUS-OOCYTES [J].
VANWINKLE, LJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1154 (02) :157-172
[19]   CATION AND HARMALINE INTERACTIONS WITH NA+-INDEPENDENT DIBASIC AMINO-ACID-TRANSPORT SYSTEM-Y+ IN HUMAN ERYTHROCYTES AND IN ERYTHROCYTES FROM A PRIMITIVE VERTEBRATE THE PACIFIC HAGFISH (EPTATRETUS-STOUTI) [J].
YOUNG, JD ;
FINCHAM, DA ;
HARVEY, CM .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1070 (01) :111-118