Polarized function of thick ascending limbs of Henle cells in osmoregulation

被引:13
作者
Grunewald, RW
Oppermann, M
Schettler, V
Fiedler, GM
Jehle, PM
Schuettert, JB
机构
[1] Univ Hosp Goettingen, Dept Nephrol & Rheumatol, D-37075 Gottingen, Germany
[2] Univ Hosp Ulm, Dept Nephrol, Ulm, Germany
关键词
TALH; organic osmolytes; cell polarity; kidney medulla; epithelial cells; transport; volume regulation; glucose uptake;
D O I
10.1046/j.1523-1755.2001.00070.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background. Organic osmolytes are necessary for osmoregulation in mammalian kidney. Since renal epithelial cells in many cases possess specific mechanisms both for uptake and osmotically regulated release, we investigated their localization in polarized cells. Methods. An immortalized epithelial cell line derived from the thick ascending limb of Henle's loop (TALH) was used to examine the transport characteristics of the apical and basolateral plasma membranes for osmotic regulation of organic osmolytes. Cells were cultured on filters in a two-compartment chamber: Results. In culture under hypertonic conditions the TALH cells accumulated in the following balance: sorbitol > betaine = myo-inositol > glycerophosphoryl choline (GPC). When extracellular osmolarity was decreased, then sorbitol was released on the apical side, whereas betaine and myo-inositol efflux occurred on the basolateral side. GPC release showed no preference of either side. Taurine did not seem to be necessary for osmoregulation under these conditions. Osmotically regulated myo-inositol and betaine uptake was located on the apical side, and choline uptake took place on both sides equally. Conclusion. These results show that in renal epithelial cells, both osmotically induced release and the uptake of organic osmolytes are divided between the apical and the basolateral sides. This might be important for volume regulation.
引用
收藏
页码:2290 / 2298
页数:9
相关论文
共 37 条
[21]   Expression of betaine transporter mRNA: Its unique localization and rapid regulation in rat kidney [J].
Miyai, A ;
Yamauchi, A ;
Moriyama, T ;
Kaneko, T ;
Takenaka, M ;
Sugiura, T ;
Kitamura, H ;
Ando, A ;
Tohyama, M ;
Shimada, S ;
Imai, E ;
Kamada, T .
KIDNEY INTERNATIONAL, 1996, 50 (03) :819-827
[22]   OSMOREGULATION OF GLYCEROPHOSPHORYLCHOLINE CONTENT OF MAMMALIAN RENAL-CELLS [J].
NAKANISHI, T ;
BURG, MB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1989, 257 (04) :C795-C801
[23]  
NOLL F, 1984, METHOD ENZYMAT AN, P1521
[24]   Reabsorption of betaine in Henle's loops of rat kidney in vivo [J].
Pummer, S ;
Dantzler, WH ;
Lien, YHH ;
Moeckel, GW ;
Völker, K ;
Silbernagl, S .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (03) :F434-F439
[25]  
Ruhfus B, 1998, IN VITRO CELL DEV-AN, V34, P227
[26]   Hypotonicity-activated efflux of taurine and myo-inositol in rat inner medullary collecting duct cells: Evidence for a major common pathway [J].
Ruhfus, B ;
Kinne, RKH .
KIDNEY & BLOOD PRESSURE RESEARCH, 1996, 19 (06) :317-324
[27]  
Schmolke M, 1996, EUR J CLIN CHEM CLIN, V34, P499
[28]   MAINTENANCE OF EXPRESSION OF DIFFERENTIATED FUNCTION OF KIDNEY-CELLS FOLLOWING TRANSFORMATION BY SV40 EARLY REGION DNA [J].
SCOTT, DM ;
MACDONALD, C ;
BRZESKI, H ;
KINNE, R .
EXPERIMENTAL CELL RESEARCH, 1986, 166 (02) :391-398
[30]   Contribution of Na+-H+ exchange to sodium reabsorption in the loop of Henle:: a microperfusion study in rats [J].
Shirley, DG ;
Walter, SJ ;
Unwin, RJ ;
Giebisch, G .
JOURNAL OF PHYSIOLOGY-LONDON, 1998, 513 (01) :243-249