Phospholipase C isozymes in the human brain and their changes in Alzheimer's disease

被引:0
作者
Shimohama, S
Sasaki, Y
Fujimoto, S
Kamiya, S
Taniguchi, T
Takenawa, T
Kimura, J
机构
[1] KYOTO PHARMACEUT UNIV, DEPT ENVIRONM BIOCHEM, YAMASHIMA KU, KYOTO 607, JAPAN
[2] KYOTO PHARMACEUT UNIV, DEPT NEUROBIOL, YAMASHIMA KU, KYOTO 607, JAPAN
[3] UNIV TOKYO, INST MED SCI, DEPT BIOCHEM, MINATO KU, TOKYO 108, JAPAN
关键词
Alzheimer's disease; phospholipase C; phospholipase C-gamma 1; phospholipase C-delta 1; chromatofocusing; get filtration chromatography;
D O I
暂无
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Phosphoinositide-specific phospholipase C is a key enzyme in signal transduction. We have previously demonstrated that an isozyme of phospholipase C, phospholipase C-delta 1, accumulates aberrantly in the brains of patients with Alzheimer's disease. In the present study, we examined the property of phospholipase C isozymes in human brains using the methods of chromatofocusing and gel filtration chromatography, and investigated their changes in Alzheimer's disease brains. The chromatofocusing profile of human brain phospholipase C activity on a Mono P HR column demonstrated that phospholipase C-gamma 1, exhibiting an isoelectric point value of 5.2, and phospholipase C-delta 1, exhibiting isoelectric point values of 5.2 and 4.6, are partly overlapped in their elution. In contrast, the elution profiles of control and Alzheimer's disease brain phospholipase C on Superdex 200 pg column gel filtration chromatography indicated that phospholipase C-gamma 1 and phospholipase C-delta 1 can be separated with the elution position having a molecular weight of about 240,000 and 140,000, respectively, in the human brain. Using this gel filtration chromatography it was revealed that the phospholipase C-gamma 1 activity was significantly decreased and the phospholipase C-delta 1 activity was significantly increased in Alzheimer's disease brains compared with controls. These results suggest that the phospholipase C isozymes are differentially involved in Alzheimer's disease. (C) 1997 IBRO. Published by Elsevier Science Ltd.
引用
收藏
页码:999 / 1007
页数:9
相关论文
共 26 条
[1]   INOSITOL TRISPHOSPHATE, A NOVEL 2ND MESSENGER IN CELLULAR SIGNAL TRANSDUCTION [J].
BERRIDGE, MJ ;
IRVINE, RF .
NATURE, 1984, 312 (5992) :315-321
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]  
CHAN A, 1991, P NATL ACAD SCI USA, V359, P66
[4]  
COLEMAN PD, 1987, NEUROBIOL AGING, V8, P521, DOI 10.1016/0197-4580(87)90127-8
[5]   Crystal structure of a mammalian phosphoinositide-specific phospholipase C delta [J].
Essen, LO ;
Perisic, O ;
Cheung, R ;
Katan, M ;
Williams, RL .
NATURE, 1996, 380 (6575) :595-602
[6]   STRUCTURE OF THE HIGH-AFFINITY COMPLEX OF INOSITOL TRISPHOSPHATE WITH A PHOSPHOLIPASE-C PLECKSTRIN HOMOLOGY DOMAIN [J].
FERGUSON, KM ;
LEMMON, MA ;
SCHLESSINGER, J ;
SIGLER, PB .
CELL, 1995, 83 (06) :1037-1046
[7]  
FULOP T, 1994, DRUG AGING, V5, P366
[8]   ISOLATION AND CHARACTERIZATION OF A GAMMA-TYPE PHOSPHOINOSITIDE-SPECIFIC PHOSPHOLIPASE-C (PLC-GAMMA-2) [J].
HOMMA, Y ;
EMORI, Y ;
SHIBASAKI, F ;
SUZUKI, K ;
TAKENAWA, T .
BIOCHEMICAL JOURNAL, 1990, 269 (01) :13-18
[9]   ALZHEIMERS-DISEASE [J].
KATZMAN, R .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (15) :964-973
[10]   Molecular cloning, splice variants, expression, and purification of phospholipase C-delta 4 [J].
Lee, SB ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (01) :25-31