OSMOLARITY-SENSITIVE RELEASE OF FREE AMINO-ACIDS FROM CULTURED KIDNEY-CELLS (MDCK)

被引:58
|
作者
OLEA, RS [1 ]
PASANTESMORALES, H [1 ]
LAZARO, A [1 ]
CEREIJIDO, M [1 ]
机构
[1] CTR RES & ADV STUDIES,DEPT PHYSIOL & BIOPHYS,MEXICO CITY,MEXICO
来源
JOURNAL OF MEMBRANE BIOLOGY | 1991年 / 121卷 / 01期
关键词
MDCK CELLS; AMINO ACID RELEASE; TAURINE; VOLUME REGULATION; QUINIDINE; DIDS;
D O I
10.1007/BF01870646
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 amino acid pool of MDCK cells was essentially constituted by alanine, glycine, glutamic acid, serine, taurine, lysine, beta-alanine and glutamine. Upon reductions in osmolarity, free amino acids were rapidly mobilized. In 50% hyposmotic solutions, the intracellular content of free amino acids decreased from 69 to 25 mM. Glutamic acid, taurine and beta-alanine were the most sensitive to hyposmolarity, followed by glycine, alanine and serine, whereas isoleucine, phenylalanine and valine were only weakly reactive. The properties of this osmolarity-sensitive release of amino acids were examined using H-3-taurine. Decreasing osmolarity to 85, 75 or 50% increased taurine efflux from 0.6% per min to 1.6, 3.5 and 5.06 per min, respectively. The time course of H-3-taurine release closely follows that of the regulatory volume decrease in MDCK cells. Taurine release was unaffected by removal of Na+, Cl- or Ca2+, or by treating cells with colchicine or cytochalasin. It was temperature dependent and decreased at low pH. Taurine release was unaffected by bumetanide (an inhibitor of the Na+/K+/2Cl- carrier); it was inhibited 16 and 67 by TEA and quinidine (inhibitors of K+ conductances), unaffected by gadolinium or diphenylamine-2-carboxylate (inhibitors of Cl- channels) and inhibited 50% by DIDS. The inhibitory effects of DIDS and quinidine were additive. Quinidine but not DIDS inhibited taurine uptake by MDCK cells.
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页码:1 / 9
页数:9
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