Review

Subject Category: Review Article

British Journal of Pharmacology (2008) 153, 299–308; doi:10.1038/sj.bjp.0707523; published online 5 November 2007

CB2 receptor-mediated migration of immune cells: it can go either way

A M Miller1 and N Stella1,2

  1. 1Department of Pharmacology, University of Washington, Seattle, WA, USA
  2. 2Psychiatry and Behavioral Sciences, University of Washington, Seattle, WA, USA

Correspondence: Dr N Stella, Department of Pharmacology, Psychiatry and Behavioral Sciences, University of Washington, 1959 NE Pacific St, Seattle, WA 98115-7280, USA. E-mail: nstella@u.washington.edu

Received 29 June 2007; Revised 28 August 2007; Accepted 1 October 2007; Published online 5 November 2007.

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Abstract

Though many studies have examined the role of CB2 receptors in immune cell migration, it has been difficult to form definitive conclusions about the physiopathological role of these receptors in regulating immune responses and how this might be pharmacologically targeted for therapy. Do cannabinoids promote inflammation through the recruitment of immune cells, or reduce inflammation by interfering with the action of other chemoattractants? Is therapeutic intervention with an agonist or antagonist more appropriate for the reduction of inflammation? In this review, we will summarize the progress that has been made in answering these questions and outline current hypotheses.

Keywords:

cannabinoid, CB2, migration, chemotaxis, leukocyte

Abbreviations:

2-AG, 2-arachidonoylglycerol; abn-CBD, abnormal cannabidiol; anandamide, N-arachidonoylethanolamine; CBD, cannabidiol; Delta9-THC, Delta9-tetrahydrocannabinol; DEA, docosatetraenylethanolamide; eCBs, endocannabinoids; fMLP, formyl-methionyl-leucyl-phenylalanine; HEA, homo-gamma-linolenylethanolamide

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