Group-specific assays that distinguish between the four major types of mammalian phospholipase A2

被引:130
作者
Yang, HC
Mosior, M
Johnson, CA
Chen, YJ
Dennis, EA [1 ]
机构
[1] Univ Calif San Diego, Revelle Coll, Dept Biochem & Chem, La Jolla, CA 92093 USA
[2] Univ Calif San Diego, Sch Med, La Jolla, CA 92093 USA
关键词
D O I
10.1006/abio.1999.4053
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Phospholipase A(2) (PLA(2)) constitutes a diverse superfamily of enzymes which catalyze the deacylation of phospholipids. At least four types of PLA(2) are potentially involved in arachidonic acid release in cells and tissues. Since all of them catalyze the same enzymatic reaction, it is difficult to distinguish between them in mixtures of enzymes normally present in biological samples. Utilizing specific properties of each PLA(2), we have designed distinct assay procedures which selectively and sensitively detect each type: Group VI Ca2+-independent PLA(2), Group IV cytosolic Ca2+-dependent PLA(2), Groups V and IIA secreted PLA(2)s. Each specific assay procedure is selective for a particular PLA(2) type by at least fourfold and as high as four orders of magnitude relative to the other three enzymes. All assays can detect PLA(2) activity with as low as subnanogram quantities of enzyme, Importantly, these assays are able to differentiate and quantitate the biochemically and structurally related enzymes, Group IIA and V sPLA(2)s in crude biological samples. Employing this system, we have found that iPLA(2) is the dominant PLA(2) in rat brain, and cPLA(2) is the most abundant PLA(2) in P388D(1) macrophages and human amnionic WISH cells. (C) 1999 Academic Press.
引用
收藏
页码:278 / 288
页数:11
相关论文
共 35 条
[1]   INHIBITION OF MACROPHAGE CA2+-INDEPENDENT PHOSPHOLIPASE A(2) BY BROMOENOL LACTONE AND TRIFLUOROMETHYL KETONES [J].
ACKERMANN, EJ ;
CONDEFRIEBOES, K ;
DENNIS, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (01) :445-450
[2]  
ACKERMANN EJ, 1994, J BIOL CHEM, V269, P9227
[3]   PHOSPHOLIPASE A(2) REGULATES CRITICAL INFLAMMATORY MEDIATORS OF MULTIPLE ORGAN FAILURE [J].
ANDERSON, BO ;
MOORE, EE ;
BANERJEE, A .
JOURNAL OF SURGICAL RESEARCH, 1994, 56 (02) :199-205
[4]   Fas-induced arachidonic acid release is mediated by Ca2+-independent phospholipase A2 but not cytosolic phospholipase A2 which undergoes proteolytic inactivation [J].
Atsumi, G ;
Tajima, M ;
Hadano, A ;
Nakatani, Y ;
Murakami, M ;
Kudo, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (22) :13870-13877
[5]   Involvement of phosphatidate phosphohydrolase in arachidonic acid mobilization in human amnionic WISH cells [J].
Balboa, MA ;
Balsinde, J ;
Dennis, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (13) :7684-7690
[6]   Novel group V phospholipase A(2) involved in arachidonic acid mobilization in murine P388D(1) macrophages [J].
Balboa, MA ;
Balsinde, J ;
Winstead, MV ;
Tischfield, JA ;
Dennis, EA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (50) :32381-32384
[7]   Reduced fertility and postischaemic brain injury in mice deficient in cytosolic phospholipase A(2) [J].
Bonventre, JV ;
Huang, ZH ;
Taheri, MR ;
OLeary, E ;
Li, E ;
Moskowitz, MA ;
Sapirstein, A .
NATURE, 1997, 390 (6660) :622-625
[8]   Expression and characterization of human group V phospholipase A2 [J].
Chen, YJ ;
Dennis, EA .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1998, 1394 (01) :57-64
[9]   Multiple controls in inflammation - Extracellular and intracellular phospholipase A(2), inducible and constitutive cyclooxygenase, and inducible nitric oxide synthase [J].
Cirino, G .
BIOCHEMICAL PHARMACOLOGY, 1998, 55 (02) :105-111
[10]   Reactive glia express cytosolic phospholipase A(2) after transient global forebrain ischemia in the rat [J].
Clemens, JA ;
Stephenson, DT ;
Smalstig, EB ;
Roberts, EF ;
Johnstone, EM ;
Sharp, JD ;
Little, SP ;
Kramer, RM .
STROKE, 1996, 27 (03) :527-535