The emerging role of group VI calcium-independent phospholipase A2 in releasing docosahexaenoic acid from brain phospholipids

被引:95
作者
Green, Joshua T. [1 ]
Orr, Sarah K. [1 ]
Bazinet, Richard P. [1 ]
机构
[1] Univ Toronto, Fac Med, Dept Nutr Sci, Toronto, ON M5S 3E2, Canada
关键词
signaling; cyclooxygenase; lipoxygenase; docosanoid; neuroprotectin; uptake; turnover; kinetics; neuroinflammation; arachidonic acid;
D O I
10.1194/jlr.R700017-JLR200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Brain phospholipids are highly enriched in docosahexaenoic acid (DHA; 22:6n-3). Recent advances indicate that 22:6n-3 is released from brain phospholipids via the action of phospholipase A(2) (PLA(2)) in response to several stimuli, including neurotransmission, where it then acts as a secondary messenger. Furthermore, it is now known that released 22:6n-3 is a substrate for several oxygenation enzymes whose products are potent signaling molecules. One emerging candidate PLA(2) involved in the release of 22:6n-3 from brain phospholipids is the group VI calcium-independent phospholipase A(2) (iPLA(2)). After a brief review of brain 22:6n-3 metabolism, cell culture and rodent studies facilitating the hypothesis that group VI iPLA(2) releases 22:6n-3 from brain phospholipids are discussed. The identification of PLA(2)s involved in cleaving 22:6n-3 from brain phospholipids could lead to the development of novel therapeutics for brain disorders in which 22:6n-3 signaling is disordered.
引用
收藏
页码:939 / 944
页数:6
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