OSMOREGULATORY ALTERATIONS IN MYOINOSITOL UPTAKE BY BOVINE LENS EPITHELIAL-CELLS .3. EFFECTS OF CYCLOHEXIMIDE AND COLCHICINE ON NA+-MYO-INOSITOL COTRANSPORTER ACTIVITY UNDER HYPERTONIC CONDITIONS, INHIBITION OF A PLASMA-MEMBRANE OSMOTIC-STRESS PROTEIN

被引:5
作者
CAMMARATA, PR
CHEN, HQ
ZHOU, C
REEVES, R
机构
[1] Department of Anatomy and Cell Biology, University of North Texas, North Texas Eye Research, Fort Worth, TX 76107
关键词
HYPERTONICITY; PROTEIN SYNTHESIS; NA+-MYO-INOSITOL COTRANSPORT PROTEIN(S); OSMOREGULATION; CULTURED LENS EPITHELIAL CELLS;
D O I
10.1006/exer.1994.1083
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Cultured bovine lens epithelial cells adapt to hypertonic sodium stress via an increase in Na+-myo-inositol cotransporter activity and accumulate myo-inositol. At least 12 hr of hypertonic exposure was necessary to enhance myo-inositol accumulation; and thereafter, uptake activity continued to increase throughout the duration of a 72-hr exposure period. Switching from hypertonic to isotonic medium for 24 hr reversed the otherwise elevated accumulation activity. The protein synthesis inhibitor, cycloheximide, did not affect myo-inositol uptake in isotonic medium but markedly decreased myo-inositol uptake in hypertonic medium. Cells exposed to hypertonic conditions and the microtubule disrupter, colchicine, similarly showed marked impairment of the otherwise enhanced myo-inositol uptake. These studies indicated that hypertonicity-induced elevation of Na+-myo-inositol cotransporter activity in cultured bovine lens epithelial cells is not solely attributed to the increased sodium gradient alone, but rather involves increased de novo synthesis of the Na+-myo-inositol cotransporter protein(s).
引用
收藏
页码:83 / 89
页数:7
相关论文
共 18 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   SORBINIL PREVENTS THE HYPERGALACTOSEMIC-INDUCED REDUCTION IN [H-3] MYOINOSITOL UPTAKE AND DECREASED [H-3] MYOINOSITOL INCORPORATION INTO THE PHOSPHOINOSITIDE CYCLE IN BOVINE LENS EPITHELIAL-CELLS INVITRO [J].
CAMMARATA, PR ;
TSE, D ;
YORIO, T .
CURRENT EYE RESEARCH, 1990, 9 (06) :561-568
[3]  
CAMMARATA PR, 1988, INVEST OPHTH VIS SCI, V29, P1452
[4]  
CAMMARATA PR, 1992, INVEST OPHTH VIS SCI, V33, P3561
[5]  
CAMMARATA PR, 1992, INVEST OPHTH VIS SCI, V33, P3572
[6]  
CAMMARATA PR, 1994, INVEST OPHTH VIS SCI, V35, P1223
[7]   DEPLETION OF GLUTATHIONE BY L-BUTHIONINE SULFOXIMINE DOES NOT PROMOTE INACTIVATION OF MYOINOSITOL TRANSPORT IN CULTURED BOVINE LENS EPITHELIAL-CELLS [J].
CAMMARATA, PR ;
TSE, D ;
YORIO, T .
CURRENT EYE RESEARCH, 1991, 10 (04) :321-330
[8]   SORBITOL, MYOINOSITOL, AND ROD OUTER SEGMENT PHAGOCYTOSIS IN CULTURED HRPE CELLS EXPOSED TO GLUCOSE - INVITRO MODEL OF MYOINOSITOL DEPLETION HYPOTHESIS OF DIABETIC COMPLICATIONS [J].
DELMONTE, MA ;
RABBANI, R ;
DIAZ, TC ;
LATTIMER, SA ;
NAKAMURA, J ;
BRENNAN, MC ;
GREENE, DA .
DIABETES, 1991, 40 (10) :1335-1348
[9]   POLYOL PATHWAY ACTIVITY AND MYOINOSITOL METABOLISM - A SUGGESTED RELATIONSHIP IN THE PATHOGENESIS OF DIABETIC NEUROPATHY [J].
FINEGOLD, D ;
LATTIMER, SA ;
NOLLE, S ;
BERNSTEIN, M ;
GREENE, DA .
DIABETES, 1983, 32 (11) :988-992
[10]  
HOHMAN TC, 1991, ENZYMOLOGY MOL BIOL, V3, P139