A comprehensive profile of brain enzymes that hydrolyze the endocannabinoid 2-arachidonoylglycerol

被引:883
作者
Blankman, Jacqueline L. [1 ,2 ]
Simon, Gabriel M. [1 ,2 ]
Cravatt, Benjamin F. [1 ,2 ]
机构
[1] Scripps Res Inst, Skaggs Inst Chem Biol, La Jolla, CA 92037 USA
[2] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
来源
CHEMISTRY & BIOLOGY | 2007年 / 14卷 / 12期
关键词
D O I
10.1016/j.chembiol.2007.11.006
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
Endogenous ligands for cannabinoid receptors ("endocannabinoids") include the lipid transmitters anandamide and 2-arachidonoylglycerol (2-AG). Endocannabinoids modulate a diverse set of physiological processes and are tightly regulated by enzymatic biosynthesis and degradation. Termination of anandamide signaling by fatty acid amide hydrolase (FAAH) is well characterized, but less is known about the inactivation of 2-AG, which can be hydrolyzed by multiple enzymes in vitro, including FAAH and monoacylglycerol lipase (MAGL). Here, we have taken a functional proteomic approach to comprehensively map 2-AG hydrolases in the mouse brain. Our data reveal that similar to 85% of brain 2-AG hydrolase activity can be ascribed to MAGL, and that the remaining 15% is mostly catalyzed by two uncharacterized enzymes, ABHD6 and ABHD12. Interestingly, MAGL, ABHD6, and ABHD12 display distinct subcellular distributions, suggesting that they may control different pools of 2-AG in the nervous system.
引用
收藏
页码:1347 / 1356
页数:10
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