Two proteins with seven transmembrane-spanning domains typical of guanosine-nucleotide-bindingprotein-coupled receptors have been identified as cannabinoid receptors ; the central cannabinoid receptor, CB1, and the peripheral cannabinoid receptor, CB2, initially described in rat brain and spleen, respectively. Here, we report the distribution patterns for both CB1 and CB2 transcripts in human immune cells and in several human tissues, as analysed using a highly sensitive and quantitative PCR-based method. CB1 was mainly expressed in the central nervous system and, to a lower extent, in several peripheral tissues such as adrenal gland, heart, lung, prostate, uterus, ovary, testis, bone marrow, thymus and tonsils. In contrast, the CB2 gene, which is not expressed in the brain, was particularly abundant in immune tissues, with an expression level 10-100-fold higher than that of CB1. Although CB2 mRNA was also detected in some other peripheral tissues, its level remained very low. In spleen and tonsils, the CB2 mRNA content was equivalent to that of CB1 mRNA in the central nervous system. Among the main human blood cell subpopulations, the distribution pattern of the CB2 mRNA displayed important variations. The rank order of CB2 mRNA levels in these cells was B-cells > natural killer cells S monocytes > polymorphonuclear neutrophil cells > T8 cells > T4 cells. The same rank order was also established in human cell lines belonging to the inyeloid, monocytic and lymphoid lineages. The prevailing expression of the CB2 gene in immune tissues was confirmed by Northern-blot analysis. In addition, the expression of the CB2 protein was demonstrated by an immunohistological analysis performed on tonsil sections using specific anti-(human CB2) IgG; this experiment showed that CB2 expression was restricted to Blymphocyte-enriched areas of the mantle of secondary lymphoid follicles. These results suggest that (a) CB1 and CB2 can be considered as tissue-selective antigens of the central nervous system and immune system, respectively, and (b) cannabinoids may exert specific receptor-mediated actions on the immune system through the CB2 receptor.Keywords: cannabinoid ; cannabinoid receptors (CB1; CB2) ; human immune system ; B cells; natural killer cells.A-9-Tetrahydrocannabinol, the major active component of cannabis, as well as other cannabinoids, are known to exert a wide range of physiological effects such as drowsiness, alterations in cognition and memory, analgesia, orexigenic effects, anti-emetic effects, a decrease in intra-ocular pressure, anti-inflammatory effects and immunosuppression [l]. Many studies have been conducted to decipher the cannabinoid system. First attributed to non-specific cell membrane disruption, the major cannabinoid effects are now thought to be mediated through specific cannabinoid receptors. A guanosine-nucleotide-bindingprotein-coupled receptor of 472 amino-acid residues, CB1, was initially characterized in rat brain [Z] and further cloned both in rat [3] and human [4]. As the expression of the c...

Cannabinoids, known for their psychoactive effects, also possess iminunomodulatory properties. The recent isolation and cloning of the G-protein-coupled peripheral cannabinoid receptor (CB2), mainly expressed in immune tissues, have provided molecular tools to determine how cannabinoid compounds may mediate immunomodulation. We here investigated the CB2 signaling properties using stably transfected Chinese hamster ovary cells expressing human CB2. First, we showed that stimulation by a cannabinoid agonist activated mitogen-activated protein (MAP) kinase in time-and dose-dependent manners. The rank order of potency for MAP kinase activation of cannabinoid agonists correlated well with their binding capacities. Second, we demonstrated that, following MAP kinase activation, cannabinoids induced the expression of the growth-related gene Krox-24, also known as NGFI-A, 28268, and egr-1 .Pertussis toxin completely prevented both MAP kinase activation and Krox-24 induction, even more these responses appeared to be dependent of specific proteine kinase C isoforms and independent of inhibition of adenylyl cyclase. A similar coupling of CB2 to a mitogenic pathway and to the regulation of Krox-24 expression was also observed in human promyelocytic cells HL60. Taken together, these findings provide evidence for a functional role of the CB2 receptor in gene induction mediated by the MAP kinase network.Keywords: peripheral cannabinoid receptor; cannabinoid receptor CB2 ; mitogen-activated protein kinase ; Krox-24: cannabinoid.A'-Tetrahydrocannabinol, the major active component of marijuana as well as other cannabinoids, is known to exert a wide range of physiological effects : drowsiness, alterations in cognition and memory, analgesia, as well as anti-inflammatory and immunomodulatory effects [I, 21. Many studies have been conducted to decipher the complexity of the cannabinoid system. First attributed to nonspecific cell membrane alterations, the cannabinoid effects are now known to be mediated through cannabinoid receptors. Two proteins with seven transmembranespanning domains typical of G-protein-coupled receptors have been identified as tetrahydrocannabinol receptors and referred to as CBI and CB2.The CBI receptor is predominantly expressed in the brain [3, 41 and could account for the psychoactive effects of cannabinoids. This receptor is also found in the periphery but at a much lower abundance [5-71. Several signaling pathways triggered by the stimulation of CBI have already been described, all being sensitive to pertussis toxin (PTX). Activation of CBI inhibits adenylyl cyclase activity [8J as well as voltage-depenCorrespondence to P. Casellas, Sanofi Recherche, 371 rue du Pr. Joseph Blayac, F-34184 Montpellier cedex 04, France.Abbrevintions. MAP, mitogen-activated protein; MBP, myelin basic protein; CHO, Chinese hamster ovary; CB1, central cannabinoid receptor; CB2, peripheral cannabinoid receptor; Br*cAMP, 8-bromoadenosine 3',S'-monophosphate; Bt,cAMP, P,2'-dibutyryl-adenosine 3',S'-monophosphate; EMSA, electrophoret...

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Despite massive research efforts, the molecular etiology of bovine polledness and the developmental pathways involved in horn ontogenesis are still poorly understood. In a recent article, we provided evidence for the existence of at least two different alleles at the Polled locus and identified candidate mutations for each of them. None of these mutations was located in known coding or regulatory regions, thus adding to the complexity of understanding the molecular basis of polledness. We confirm previous results here and exhaustively identify the causative mutation for the Celtic allele (PC) and four candidate mutations for the Friesian allele (PF). We describe a previously unreported eyelash-and-eyelid phenotype associated with regular polledness, and present unique histological and gene expression data on bovine horn bud differentiation in fetuses affected by three different horn defect syndromes, as well as in wild-type controls. We propose the ectopic expression of a lincRNA in PC/p horn buds as a probable cause of horn bud agenesis. In addition, we provide evidence for an involvement of OLIG2, FOXL2 and RXFP2 in horn bud differentiation, and draw a first link between bovine, ovine and caprine Polled loci. Our results represent a first and important step in understanding the genetic pathways and key process involved in horn bud differentiation in Bovidae.

This study examined the effect of cannabinoid ligands on human tonsillar B-cells activated either through cross-linking of surface immunoglobulins or ligation of the CD40 antigen. The two synthetic cannabinoids, CP55,940 and WIN55212-2, as well as Ag-tetrahydrocannabinol (THC), the psychoactive component of marijuana, caused a dose-dependent increase of B-cell proliferation and displayed ECso at low nanomolar concentrations. This cannabinoid-induced enhancing activity was inhibited by pertussis toxin which suggested a G-protein-coupled receptor process. In addition, the absence of antagonistic effect of SR141716A, a specific CB1 receptor antagonist, together with the demonstration that human B-cells displayed large amount of CB2 receptor mRNAs, led us to assume that the growth enhancing activity observed on B-cells at very low concentrations of cannabinoids could be mediated through the CB2 receptor.