Phospholipase A2:: Its usefulness in laboratory diagnostics

被引:32
作者
Kaiser, E [1 ]
机构
[1] Univ Vienna, Dept Med Chem, A-1010 Vienna, Austria
关键词
phospholipase A(2); eicosanoids; inflammation; pancreatitis; multiple organ failure; septic shock; rheumatoid arthritis; acute phase protein;
D O I
10.1080/10408369991239187
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Phospholipase A(2) (PLA(2)) is an enzyme that catalyzes the hydrolysis of membrane phospholipids. This article reviews the source and structure of PLA(2), the involvement of the enzyme in various biological and pathological phenomena, and the usefulness of PLA(2) assays in laboratory diagnostics. Of particular importance is the role of PLA(2) in the cellular production of mediators of inflammatory response to various stimuli. Assays for PLA(2) activity and mass concentration are discussed, and the results of enzyme determinations in plasma from patients with different pathological conditions are presented. The determination of activity and mass concentration in plasma is particularly useful in the diagnosis and prognosis of pancreatitis, multiple organ failure, septic shock, and rheumatoid arthritis. A very important result is the demonstration that PLA(2) is an acute phase protein, like CRP. indeed, there is a close correlation between PLA(2) mass concentration and CRP levels in several pathological conditions. Although the determination of C-reactive protein is much easier to perform. and is routinely carried out in most clinical laboratories, the assessment of PLA(2) activity of mass concentration has to be considered as a reliable approach to obtain a deeper understanding of some pathological conditions and may offer additional information concerning the prognosis of several disorders.
引用
收藏
页码:65 / 163
页数:99
相关论文
共 677 条
[1]  
AARSMAN AJ, 1989, J BIOL CHEM, V264, P10008
[2]   Purification and characterization of Ca2+-dependent phospholipases A(2) from rat kidney [J].
Aarsman, AJ ;
Schalkwijk, CG ;
Neys, FW ;
Iijima, N ;
Wherrett, JR ;
vandenBosch, H .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1996, 331 (01) :95-103
[3]   MECHANISM OF ARACHIDONIC-ACID LIBERATION DURING ISCHEMIA IN GERBIL CEREBRAL-CORTEX [J].
ABE, K ;
KOGURE, K ;
YAMAMOTO, H ;
IMAZAWA, M ;
MIYAMOTO, K .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (02) :503-509
[4]  
Abe T, 1997, INT J CANCER, V74, P245, DOI 10.1002/(SICI)1097-0215(19970620)74:3<245::AID-IJC2>3.0.CO
[5]  
2-Z
[6]   MAMMALIAN CALCIUM-INDEPENDENT PHOSPHOLIPASE A(2) [J].
ACKERMANN, EJ ;
DENNIS, EA .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1995, 1259 (02) :125-136
[7]  
ACKERMANN EJ, 1994, J BIOL CHEM, V269, P9227
[8]  
AHO HJ, 1977, ACTA OTO-LARYNGOL, V117, P860
[9]   GESTATIONAL TISSUE PHOSPHOLIPASE-A2 MESSENGER-RNA CONTENT AND THE ONSET OF SPONTANEOUS LABOR IN THE HUMAN [J].
AITKEN, MA ;
RICE, GE ;
BRENNECKE, SP .
REPRODUCTION FERTILITY AND DEVELOPMENT, 1990, 2 (05) :575-580
[10]   RELATIVE ABUNDANCE OF HUMAN PLACENTAL PHOSPHOLIPASE-A2 MESSENGER-RNA IN LATE PREGNANCY [J].
AITKEN, MA ;
RICE, G ;
BRENNECKE, S .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 1992, 43 (04) :361-370