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Compartmentalization of endocannabinoids into lipid rafts in a dorsal root ganglion cell line.
Br J Pharmacol. 2008 Jan; 153(2):380-9.BJ

Abstract

BACKGROUND AND PURPOSE

N-arachidonoyl ethanolamine (AEA) and 2-arachidonoyl glycerol (2-AG) are endogenous cannabinoids binding to the cannabinoid receptors CB1 and CB2 to modulate neuronal excitability and synaptic transmission in primary afferent neurons. To investigate the compartmentalization of the machinery for AEA and 2-AG signalling, we studied their partitioning into lipid raft fractions isolated from a dorsal root ganglion X neuroblastoma cell line (F-11).

EXPERIMENTAL APPROACH

F-11 cells were homogenized and fractionated using a detergent-free OptiPrep density gradient. All lipids were partially purified from methanolic extracts of the fractions on solid phase cartridges and quantified using liquid chromatography tandem mass spectrometry (LC/MS/MS). Protein distribution was determined by Western blotting.

KEY RESULTS

Under basal conditions, the endogenous cannabinoid AEA was present in both lipid raft and specific non-lipid raft fractions as was one of its biosynthetic enzymes, NAPE-PLD. The 2-AG precursor 1-stearoyl-2-arachidonoyl-sn-glycerol (DAG), diacylglycerol lipase alpha (DAGLalpha), which cleaves DAG to form 2-AG, and 2-AG were all co-localized with lipid raft markers. CB1 receptors, previously reported to partition into lipid raft fractions, were not detected in F-11 membranes, but CB2 receptors were detected at high levels and partitioned into non-lipid raft fractions.

CONCLUSIONS AND IMPLICATIONS

The biochemical machinery for the production of 2-AG via the putative diacylglycerol pathway is localized within lipid rafts, suggesting that 2-AG synthesis via DAG occurs within these microdomains. The observed co-localization of AEA, 2-AG, and their synthetic enzymes with the reported localization of CB1 raises the possibility of intrinsic-autocrine signalling within lipid raft domains and/or retrograde-paracrine signalling.

Authors+Show Affiliations

Department of Psychological and Brain Sciences and the Gill Center for Biomolecular Sciences, Indiana University, Bloomington, IN 47405, USA.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

17965731

Citation

Rimmerman, N, et al. "Compartmentalization of Endocannabinoids Into Lipid Rafts in a Dorsal Root Ganglion Cell Line." British Journal of Pharmacology, vol. 153, no. 2, 2008, pp. 380-9.
Rimmerman N, Hughes HV, Bradshaw HB, et al. Compartmentalization of endocannabinoids into lipid rafts in a dorsal root ganglion cell line. Br J Pharmacol. 2008;153(2):380-9.
Rimmerman, N., Hughes, H. V., Bradshaw, H. B., Pazos, M. X., Mackie, K., Prieto, A. L., & Walker, J. M. (2008). Compartmentalization of endocannabinoids into lipid rafts in a dorsal root ganglion cell line. British Journal of Pharmacology, 153(2), 380-9.
Rimmerman N, et al. Compartmentalization of Endocannabinoids Into Lipid Rafts in a Dorsal Root Ganglion Cell Line. Br J Pharmacol. 2008;153(2):380-9. PubMed PMID: 17965731.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Compartmentalization of endocannabinoids into lipid rafts in a dorsal root ganglion cell line. AU - Rimmerman,N, AU - Hughes,H V, AU - Bradshaw,H B, AU - Pazos,M X, AU - Mackie,K, AU - Prieto,A L, AU - Walker,J M, Y1 - 2007/10/29/ PY - 2007/10/30/pubmed PY - 2008/4/3/medline PY - 2007/10/30/entrez SP - 380 EP - 9 JF - British journal of pharmacology JO - Br J Pharmacol VL - 153 IS - 2 N2 - BACKGROUND AND PURPOSE: N-arachidonoyl ethanolamine (AEA) and 2-arachidonoyl glycerol (2-AG) are endogenous cannabinoids binding to the cannabinoid receptors CB1 and CB2 to modulate neuronal excitability and synaptic transmission in primary afferent neurons. To investigate the compartmentalization of the machinery for AEA and 2-AG signalling, we studied their partitioning into lipid raft fractions isolated from a dorsal root ganglion X neuroblastoma cell line (F-11). EXPERIMENTAL APPROACH: F-11 cells were homogenized and fractionated using a detergent-free OptiPrep density gradient. All lipids were partially purified from methanolic extracts of the fractions on solid phase cartridges and quantified using liquid chromatography tandem mass spectrometry (LC/MS/MS). Protein distribution was determined by Western blotting. KEY RESULTS: Under basal conditions, the endogenous cannabinoid AEA was present in both lipid raft and specific non-lipid raft fractions as was one of its biosynthetic enzymes, NAPE-PLD. The 2-AG precursor 1-stearoyl-2-arachidonoyl-sn-glycerol (DAG), diacylglycerol lipase alpha (DAGLalpha), which cleaves DAG to form 2-AG, and 2-AG were all co-localized with lipid raft markers. CB1 receptors, previously reported to partition into lipid raft fractions, were not detected in F-11 membranes, but CB2 receptors were detected at high levels and partitioned into non-lipid raft fractions. CONCLUSIONS AND IMPLICATIONS: The biochemical machinery for the production of 2-AG via the putative diacylglycerol pathway is localized within lipid rafts, suggesting that 2-AG synthesis via DAG occurs within these microdomains. The observed co-localization of AEA, 2-AG, and their synthetic enzymes with the reported localization of CB1 raises the possibility of intrinsic-autocrine signalling within lipid raft domains and/or retrograde-paracrine signalling. SN - 0007-1188 UR - https://www.unboundmedicine.com/medline/citation/17965731/Compartmentalization_of_endocannabinoids_into_lipid_rafts_in_a_dorsal_root_ganglion_cell_line_ L2 - https://doi.org/10.1038/sj.bjp.0707561 DB - PRIME DP - Unbound Medicine ER -