Cloning of the first sn1-DAG lipases points to the spatial and temporal regulation of endocannabinoid signaling in the brain.

The Journal of cell biology (2003-11-12)
Tiziana Bisogno, Fiona Howell, Gareth Williams, Alberto Minassi, Maria Grazia Cascio, Alessia Ligresti, Isabel Matias, Aniello Schiano-Moriello, Praveen Paul, Emma-Jane Williams, Uma Gangadharan, Carl Hobbs, Vincenzo Di Marzo, Patrick Doherty
RESUMEN

Diacylglycerol (DAG) lipase activity is required for axonal growth during development and for retrograde synaptic signaling at mature synapses. This enzyme synthesizes the endocannabinoid 2-arachidonoyl-glycerol (2-AG), and the CB1 cannabinoid receptor is also required for the above responses. We now report on the cloning and enzymatic characterization of the first specific sn-1 DAG lipases. Two closely related genes have been identified and their expression in cells correlated with 2-AG biosynthesis and release. The expression of both enzymes changes from axonal tracts in the embryo to dendritic fields in the adult, and this correlates with the developmental change in requirement for 2-AG synthesis from the pre- to the postsynaptic compartment. This switch provides a possible explanation for a fundamental change in endocannabinoid function during brain development. Identification of these enzymes may offer new therapeutic opportunities for a wide range of disorders.

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Monoclonal Anti-Neurofilament 160 antibody produced in mouse, clone NN18, ascites fluid