INVIVO FORMATION OF POLYPHOSPHOINOSITIDE ISOMERS AND ASSOCIATION WITH PROGRESSION OF MURINE POLYCYSTIC KIDNEY-DISEASE

被引:13
作者
AUKEMA, HM
CHAPKIN, RS
TOMOBE, K
TAKAHASHI, H
HOLUB, BJ
机构
[1] TEXAS A&M UNIV SYST,DEPT ANIM SCI,MOLEC & CELL BIOL GRP,COLL STN,TX 77843
[2] TEXAS A&M UNIV SYST,GRAD FAC NUTR,COLL STN,TX 77843
[3] TEXAS AGR EXPTL STN,COLL STN,TX 77843
[4] FUJITA HLTH UNIV,ANIM CTR LAB,AICHI 47011,JAPAN
关键词
D O I
10.1016/0014-4800(92)90047-F
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Polyphosphoinositide isomers have been demonstrated to be important mediators of cell proliferation in vitro. The present study demonstrates, for the first time, the in vivo formation of the novel isomer, phosphatidylinositol(3)phosphate, in the kidney and liver of intact animals following intraperitoneal administration of [3H]myo-inositol. The formation of renal [3H]phosphatidylinositol(3)phosphate relative to total [3H]phosphatidylinositol-phosphate was positively correlated with cyst proliferation and renal enlargement in a murine model of polycystic kidney disease. Furthermore, despite no difference in the formation of renal [3H]phosphatidylinositol(4)phosphate, a markedly lower accumulation (by 48%) of [3H]phosphatidylinositol(4,5)bisphosphate was observed in the diseased animals as compared to controls. These results indicate that further studies on the in vivo formation of specific polyphosphoinositide isomers in disease states characterized by abnormal growth and oncogene expression are warranted. © 1992.
引用
收藏
页码:39 / 46
页数:8
相关论文
共 43 条
[1]  
ALLEN D, 1978, BIOCHIM BIOPHYS ACTA, V508, P277
[2]  
[Anonymous], 1991, PRINCIPLES PROCEDURE
[3]  
AUGER KR, 1991, CANCER CELL-MON REV, V3, P263
[4]   PDGF-DEPENDENT TYROSINE PHOSPHORYLATION STIMULATES PRODUCTION OF NOVEL POLYPHOSPHOINOSITIDES IN INTACT-CELLS [J].
AUGER, KR ;
SERUNIAN, LA ;
SOLTOFF, SP ;
LIBBY, P ;
CANTLEY, LC .
CELL, 1989, 57 (01) :167-175
[5]  
AVNER ED, 1990, KIDNEY INT, V37, P190
[6]   INOSITOL PHOSPHATES AND CELL SIGNALING [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1989, 341 (6239) :197-205
[7]   ONCOGENES AND SIGNAL TRANSDUCTION [J].
CANTLEY, LC ;
AUGER, KR ;
CARPENTER, C ;
DUCKWORTH, B ;
GRAZIANI, A ;
KAPELLER, R ;
SOLTOFF, S .
CELL, 1991, 64 (02) :281-302
[8]   PHOSPHOINOSITIDE KINASES [J].
CARPENTER, CL ;
CANTLEY, LC .
BIOCHEMISTRY, 1990, 29 (51) :11147-11156
[9]   REQUIREMENT FOR INTRINSIC PROTEIN TYROSINE KINASE IN THE IMMEDIATE AND LATE ACTIONS OF THE EGF RECEPTOR [J].
CHEN, WS ;
LAZAR, CS ;
POENIE, M ;
TSIEN, RY ;
GILL, GN ;
ROSENFELD, MG .
NATURE, 1987, 328 (6133) :820-823
[10]   ALKALINE-O-]N-TRANSACYLATION - A NEW METHOD FOR THE QUANTITATIVE DEACYLATION OF PHOSPHOLIPIDS [J].
CLARKE, NG ;
DAWSON, RMC .
BIOCHEMICAL JOURNAL, 1981, 195 (01) :301-306