PHOSPHOLIPASE-A2 ENZYMES - REGULATION AND INHIBITION

被引:279
作者
GLASER, KB
MOBILIO, D
CHANG, JY
SENKO, N
机构
[1] Wyeth-Ayerst Research, Princeton, NJ 08543
[2] Wyeth-Ayerst Research, Princeton, NJ 08543
[3] N. Senko is Senior Chemist in Molecular Modeling, Wyeth-Ayerst Research, Princeton, NJ 08543
[4] J.Y. Chang's current position is President and CEO of Osteoarthritis Sciences Inc., 1 Kendall Square, Bldg 200, Cambridge
关键词
D O I
10.1016/0165-6147(93)90071-Q
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The phospholipase A2 enzymes are important components of the cellular machinery that responds to inflammatory stimuli and maintains cell homeostasis by membrane remodelling. Their role as the rate-limiting step in the production of pro-inflammatory lipid mediators makes these enzymes an important therapeutic target for the treatment of inflammatory disorders. Keith Glaser and colleagues explain how the two major groups of phospholipase A2, the secretory and cytosolic forms, are very different both structurally and enzymatically. Understanding the relative contributions of these different forms of phospholipase A2 to physiological and pathological conditions requires greater insight into their cellular regulation and the development of selective inhibitors.
引用
收藏
页码:92 / 98
页数:7
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