Preparations derived from Cannabis sativa (marijuana and hashish) have become widespread since ancient times, both as therapeutic agents and in recreational smoking [1–3]. Among the more than 60 phytocannabinoids identified in Cannabis extracts, the two most abundant are Δ9-tetrahydrocannabinol (THC), the major psychotropic constituent, and cannabidiol (CBD), the major non-psychoactive component. Cannabinoids were shown to exert a wide range of therapeutic effects, and many of the cannabinoids, especially CBD, were shown to possess potent anti-inflammatory and immunomodulatory activities [4–15]. In addition, it was shown that several cannabinoids have pro-apoptotic, neuroprotective, and antitumor properties [16, 17].
The biological activities of cannabinoids are mostly mediated through cannabinoid receptors, the CB1 (primarily, but not exclusively, expressed in the central nervous system) and the CB2 (mainly expressed in immune cells) [18, 19, and references therein]. However, cannabinoids were also shown to act via mechanisms independent of CB1 and CB2. For example, CBD has very low affinity for both CB1 and CB2receptors and is therefore devoid of the psychotropic effects produced by Cannabis or THC that are mediated via CB1[4, 20]. Therefore, the anti-inflammatory activities of CBD do not seem to be mediated via either CB1 or CB2[21 and references therein].
Several groups including ours have shown that various microglial cell functions are affected by cannabinoids, including CBD. For example, our group reported that THC and CBD differentially inhibit the lipopolysaccharide (LPS)-activated nuclear factor κB (NF-κB) and interferon β/signal transducers and activators of transcription (IFN-β/STAT) pro-inflammatory pathways in a CB1/CB2-independent manner  and that CBD affects the expression of genes related to oxidative stress and glutathione (GSH) deprivation via the general control non-derepressible 2 (GCN2)/eukaryotic initiation factor 2α (eIF2α)/p8/ATF4/CHOP-tribbles homologue 3 (Trb3) pathway [11, 12]. In addition, CBD-stimulated genes were shown to be controlled by nuclear factors known to be involved in the regulation of stress response and inflammation, mainly through the [electrophile response element (EpRE)/antioxidant response element (ARE)]-nuclear factor-erythroid 2-related factor 2 (Nrf2)/ATF4 system and the Nrf2/Hmox1 axis [11, 12].
CBD was also shown to alleviate the pathological symptoms in a demyelinating disease, the experimental autoimmune encephalomyelitis (EAE), commonly used as a model of multiple sclerosis (MS). Our group reported that CBD ameliorated the severity of EAE in myelin oligodendrocyte glycoprotein 35–55 (MOG35–55)-immunized mice and attenuated microglial activation and T-cell recruitment in these CBD-treated, MOG35–55-induced EAE mice . Moreover, we were able to show that CBD inhibited the in vitro MOG-induced proliferation of MOG35–55-reactive T cells (TMOG) cells and markedly reduced their Th17 inflammatory phenotype [8, 9].
Several CBD derivatives were also shown to have anti-inflammatory and anti-proliferative properties [22, 23]. In view of the therapeutic potential of CBD, we were interested in looking into the activity of its synthetic non-psychoactive derivative, the dimethylheptyl-cannabidiol (DMH-CBD). DMH-CBD has been reported to induce apoptosis of human acute myeloid leukemia HL-60 cells  and was reported to inhibit the production of reactive oxygen intermediates, nitric oxide, and tumor necrosis factor alpha (TNFα) in LPS-activated RAW macrophages . In the present work, we studied the transcriptional effects mediated by DMH-CBD within genes involved in the regulation of stress response and inflammation in LPS-activated BV-2 microglial cells. In addition, we studied the effects of DMH-CBD on the proliferation of MOG35–55-activated TMOG cells. The results show that DMH-CBD induces similar anti-inflammatory, anti-proliferative, and stress response effects to those previously observed for CBD.
Materials and methods
LPS (Escherichia coli serotype 055:B5) was obtained from Sigma (St. Louis, MO, USA). LPS was dissolved in water, stock solutions (1 mg/mL) were stored in aliquots at −20 °C and diluted in culture medium before experiments. Lyophilized MOG35–55 peptide (MEVGWYRSPFSRVVHLYRNGK) purchased from GenScript (Piscataway, NJ, USA) was reconstituted in sterile phosphate buffered solution (PBS) and the stock solution stored in aliquots at −20 °C. (−)-5′-DMH-CBD was synthesized as previously described . Stock solution of DMH-CBD was prepared in ethanol and diluted into culture medium before experiments. The final concentrations of ethanol in the experiments did not exceed 0.1%–0.2% and had no effect on the results. Fetal calf serum and other tissue culture medium and reagents were obtained from Biological Industries (Kibbutz Beit Haemek, Israel).
Microglial cell culture
The BV-2 mouse microglial cell line was kindly provided by Prof. E. J. Choi from Korea University (Seoul, South Korea). Cells were grown in Dulbecco’s modified Eagle’s medium containing 4.5 g/L glucose and 1 mM sodium pyruvate and supplemented with 5% fetal calf serum, penicillin (100 U/mL), and streptomycin (100 μg/mL) under a humidified 5% CO2atmosphere at 37 °C. Cells (1×106 cells in 100-mm plates) were pretreated for 2 h with DMH-CBD, at the doses indicated in the text, followed by addition of LPS (100 ng/mL) for another 4 h.
RNA extraction and quantitative real-time PCR (qPCR)
Extraction, quantification, and quality of extracted RNA were performed and analyzed as described previously . copy DNA (cDNA) was synthesized using the QuantiTect Reverse Transcription kit according to the manufacturer’s instructions (Qiagen AG, Basel, Switzerland). qPCR was carried out as detailed previously . Expression levels of genes were normalized to the reference gene β2-microglobulin (B2m), whose expression has been found not to be affected by the treatments and are expressed as fold change as reported earlier . Primer sets were designed using the PrimerQuest, an online tool provided by Integrated DNA Technologies (http://eu.idtdna.com/Primerquest/Home/Index) and synthesized by Metabion International (Planegg-Steinkirchen, Germany). GenBank™ accession numbers for the different genes and the primer sequences used for amplification were reported earlier [9, 11]. The qPCR runnings were repeated three times using mRNA preparations from three independent experiments.
Encephalitogenic T-cell proliferation
TMOG raised from MOG35–55 immunized mice was obtained and maintained as previously described [8, 9, 27]. To assay the effect of DMH-CBD on TMOG proliferation, TMOG cells were cultured in 96-well plates (1.25×104 cells/well) together with splenic antigen-presenting cells (APCs; 5×105 cells/well). APCs were irradiated (25 Gy) before co-culturing to prevent them from proliferation. The co-cultured cells (TMOG/APCs) were maintained in 0.2 mL of RPMI medium containing 2.5% fetal calf serum, supplemented with streptomycin (100 μg/mL), penicillin (100 U/mL), 2 mM L-glutamine, and 50 μM β-mercaptoethanol. DMH-CBD at final doses of 0.1, 1, 5, and 10 μM was added to the cells together with the MOG35–55peptide at either 1 or 2.5 μg/mL. The cells were then incubated for 72 h at 37 °C in 5% CO2-humidified air. Cell proliferation was measured by pulsing the cells with [3H]thymidine (0.5 μCi/well; Perkin Elmer, Boston, MA, USA) for the last 16 h of the incubation period, and the cells were then harvested and counted using a Matrix 96 Direct β-counter (Packard Instruments, Meriden, CT, USA). The proliferative responses of the TMOG cells in each well were converted to percentage values with MOG35–55 effect expressed as 100%. Percentage values are calculated from the stimulation index data, which are the fold changes in mean counts per minutes (cpm) of MOG35–55 cultures over mean cpm of cultures without MOG (spontaneous proliferation). Statistical analysis was performed on percentage values [8, 27].
Data are expressed as the mean±SEM of three independent experiments and analyzed for statistical significance using Student’s t-test or one-way analysis of variance (ANOVA), followed by Dunnett’s or Newman-Keul’s post hoc test. p<0.05 was considered significant. GraphPad Prism 5 software (La Jolla, CA, USA) was used for statistical analysis of the data.
DMH-CBD treatment downregulates mRNA expression of LPS-upregulated pro-inflammatory genes in BV-2 cells
BV-2 cells were pretreated for 2 h with DMH-CBD (1, 5, and 10 μM) and then stimulated with LPS (100 ng/mL) for an additional 4 h. The control treatment with DMH-CBD alone lasted for 6 h and with LPS alone for 4 h. These treatment time points were chosen following our previous reports [7, 11]. The cells were then collected, mRNA extracted, and the expression of several genes determined by qPCR. qPCR analysis showed strong upregulation in the mRNA levels of Il1b, Il6, and Tnf following LPS stimulation of microglial cells (Figure 1A–C). Treatment with DMH-CBD significantly decreased, in a dose-dependent manner, the LPS-upregulated expression of Il1b mRNA [by 88% at 10 μM DMH-CBD; ANOVA F(4,10)=187.9, p<0.001] and of Il6 [by 82% at 10 μM DMH-CBD; ANOVA F(4,10)=9.97, p<0.01] (Figure 1A,B). The level of LPS-upregulated Tnf mRNA was also decreased by DMH-CBD, reaching a 48% reduction at 10 μM DMH-CBD, a result that unexpectedly was found to be not statistically significant [ANOVA F(4,10)=4.6, p<0.05] (Figure 1C). As shown in Figure 2, DMH-CBD by itself (without LPS) also reduced the basal transcript levels of Il1b, Il6, and Tnf in a dose-dependent manner. At a dose of 10 μM, DMH-CBD decreased the expression of Il1b mRNA by 82% [ANOVA F(3,18)=27.2, p<0.001], Il6 by 67% [ANOVA F(3,18)=14.4, p<0.01, and Tnf by 66% [ANOVA F(3,18)=43.4, p<0.001].
DMH-CBD treatment upregulates mRNA expression of genes related to oxidative stress and GSH homeostasis in BV-2 cells
qPCR analysis demonstrated that incubation of BV-2 cells with DMH-CBD (at 10 μM) leads to upregulation of several genes related to stress and GSH homeostasis (Figure 3A–F). These included tribbles homologue 3 [Trb3; by 10-fold; ANOVA F(3,8)=94.1, p<0.001], solute carrier family 7, member 11 [cystine/glutamate transporter subunit Slc7a11/xCT; by 5.4-fold; ANOVA F(3,12)=132.4, p<0.001], and heme oxygenase 1 [Hmox1; by 4-fold; ANOVA F(3,8)=49.1, p<0.001]. DMH-CBD also increased the expression of several other genes, but to a significantly lower extent, such as the activating transcription factor 4 [Atf4; by 60%; ANOVA F(3,8)=60.3, p<0.001], C/EBP homologous protein [Chop/Ddit3/Gadd153; by 50%; ANOVA F(3,8)=49.1, p<0.001], and nuclear protein 1 [Nupr1/p8; by 36%; ANOVA F(3,8)=240.1, p<0.001]. The expressions of Trb3, Hmox1, and Atf4 mRNAs were not affected by LPS. Meanwhile, Slc7a11/xCT mRNA (Figure 3B) was highly upregulated by LPS (by 8.2-fold, p<0.05) and synergistically upregulated by the combined DMH-CBD+LPS treatment (by 34-fold vs. control, p<0.001, and by 3.7-fold vs. LPS, p<0.001). p8 expression was upregulated by LPS by 3.4-fold (p<0.01) and by the combination of DMH-CBD+LPS by 4.8-fold vs. control (p<0.01) and by 40% vs. LPS (p<0.01) (Figure 3F). In contrast, Chop mRNA was slightly downregulated by LPS (by 30%, p<0.01) (Figure 3E).
DMH-CBD inhibits MOG35-55-induced TMOG cell proliferation
We previously showed that CBD ameliorates clinical symptoms of MOG35–55-induced EAE . Moreover, we showed that CBD inhibits the MOG35–55-induced proliferation of TMOG cells co-cultured with irradiated APCs in the presence of MOG35–55 . Therefore, we have analyzed the effect of DMH-CBD in this in vitro model of MOG35–55-stimulated encephalitogenic T cells. TMOG/APCs were co-cultured in the presence of MOG35–55 at a dose of 1 or 2.5 μg/mL. These concentrations were chosen following our previous reports [8, 9]. T-cell proliferation was analyzed using [3H]thymidine incorporation as previously reported . Incubation with 1 μg/mL MOG35–55 resulted in a 24±11-fold increase (p<0.05, Student’s t-test) in TMOG proliferation and incubation with 2.5 μg/mL MOG35–55 produced a 42±10-fold increase (p<0.01, Student’s t-test) in TMOG proliferation vs. non-stimulated cells (Figure 4A). Results presented in Figure 4B,C shows the inhibitory effect of DMH-CBD at various doses (0.1–10 μM) on the MOG35–55-induced proliferation of TMOG cells stimulated by either 1 or 2.5 μg/mL of MOG35–55. As shown in Figure 4B, addition of 5 μM DMH-CBD to 1 μg/mL MOG35–55-stimulated TMOG/APCs resulted in inhibition of TMOG proliferation by 51%, whereas 10 μM DMH-CBD inhibited TMOG proliferation by 97% (p<0.01). Similar results were observed when TMOG cells were stimulated with 2.5 μg/mL of MOG35–55 (Figure 4C). In this case, 5 μM DMH-CBD inhibited the proliferation by 62% (p<0.01) and 10 μM DMH-CBD by 97% (p<0.001). Lower doses of DMH-CBD (e.g. 0.1 and 1 μM) had no significant effect on TMOG proliferation induced by MOG35–55at either 1 or 2.5 μg/mL.
The present study describes the effects of DMH-CBD on inflammatory and stress-related genes in BV-2 microglial cells and on the proliferation of MOG35–55-activated TMOG cells.
We found that DMH-CBD downregulates in a dose-dependent manner the mRNA expression of LPS-upregulated Il1b and Il6 transcripts. Moreover, DMH-CBD dose dependently downregulates the expression of these transcripts in unstimulated BV-2 cells. These findings show that DMH-CBD possesses anti-inflammatory and protective properties. DMH-CBD effects are similar to those found for CBD in our previous work [7, 11, 13] where we reported that CBD decreases the production and release of the pro-inflammatory cytokines IL-1b and IL-6, but not of TNFα in LPS-stimulated BV-2 microglial cells [7, 13].
In addition, we show here that DMH-CBD strongly upregulates the expression of the genes Trb3, Slc7a11/xCT, and Hmox1 and, to a lesser extent, of the genes Atf4, Chop/Ddit3/Gadd153, and p8/Nupr1. Previous work from our laboratory showed that these genes were also significantly upregulated by CBD . Most of these genes (Trb3, Slc7a11/xCT, Atf4, Chop/Ddit3/Gadd153, and p8/Nupr1) are known to contain amino acid response elements and to be regulated in response to amino acid deprivation . The upregulation of these amino acid-response genes suggests an effect of DMH-CBD on GCN2/eIF2α/ATF4-mediated stress pathway [29–31]. These results demonstrate that DMH-CBD is inducing a metabolic adaptation program typical for nutrient limiting conditions, characterized by repression of protein synthesis and upregulation of amino acid biosynthesis and transporter genes .
Another gene upregulated by DMH-CBD is Nupr1/p8 (36%). Nupr1/p8 was found to be induced by ATF4 in response to various cellular stressors, and its expression was associated with enhanced transcriptional activation of genes downstream of ATF4 (such as Chop and Trb3). This suggests that p8 promotes the transcription of stress-regulated genes via a positive feedback on ATF4 pathway . Other cannabinoids like CBD, THC, and the synthetic WIN 55,212-2 were also shown to induce p8 expression [11, 34, 35]. In addition, our results show upregulation of p8 mRNA expression by LPS, an effect also shown by others , and by the combined treatment of DMH-CBD+LPS.
As described above, DMH-CBD highly upregulated the expression of the mRNA of the transporter Slc7a11/xCT and of the antioxidant inducible enzyme Hmox1, both known to be modulated in response to oxidative stress via the ARE/EpRE-Nrf2 system . The Slc7a11/xCT constitutes the stress inducible subunit of the cystine/glutamate transport system xc− [38, 39] whose activation will produce an increase in the levels of GSH in the cells . In addition, we show that LPS strongly upregulates Slc7a11/xCT mRNA expression and that the effect of LPS and DMH-CBD applied together on Slc7a11/xCT expression is synergistic. This result is in agreement with Sato et al. , who reported that LPS induces the activity of the cystine/glutamate transporter in macrophages, increasing GSH levels in the cells. Moreover, they showed partial synergism when macrophages were incubated with LPS together with TNFα.
Redox homeostasis was reported to modulate the microglia and macrophages M1/M2 polarization . In this regard, it was shown that Hmox1 induction drives a shift to M2 macrophage phenotype, characterized by its intracellular redox status, consisting of high expression of scavenging molecules and GSH [42, 43]. Thus, upregulation of Slc7a11/xCT and Hmox1 by DMH-CBD may serve to protect the cells by inducing an adaptive cellular response against inflammatory stimuli and oxidative injury, utilizing GSH as antioxidant or conjugating/detoxifying agent.
In the present study, we also report that DMH-CBD significantly decreases MOG35–55-induced TMOG cell proliferation. This result is in agreement with our previous work, which shows that CBD inhibits the MOG35–55-induced proliferation of TMOG cells stimulated with MOG35–55 . Cannabinoids, including CBD, have been shown to possess anti-proliferative properties in highly proliferative cell lines, including transformed T-cell lines [44–46]. For example, CBD inhibits proliferation by inducing cell death in cancer cell lines via the transient receptor potential vanilloid channel 2 [47, 48] and THC reduces proliferation and leads to cell death of C6 glioma cells via CB1 receptor . As for DMH-CBD, it was shown that DMH-CBD (as well as CBD) in combination with γ-irradiation induces apoptotic cell death of HL-60 myeloblastic leukemia cells . Here, we show that DMH-CBD in similarity to previous results with CBD [8, 9, 50] can prevent the proliferation of primary T cells.
Altogether, our results show that DMH-CBD, a non-psychoactive, synthetic CBD derivative, has anti-inflammatory and anti-proliferative properties. DMH-CBD induces the expression of genes related to oxidative stress and amino acid deprivation, genes that are controlled by Nrf2 and ATF4 transcription factors. In addition, DMH-CBD inhibits the proliferation of MOG35–55-activated TMOG cells. In similarity to CBD, DMH-CBD could be of high therapeutic value in neuro-inflammatory diseases and related syndromes.
A.J. is supported by the Israeli Ministry for Absorption in Science.
Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.
Research funding: This work was supported by the Dr. Miriam and Sheldon G. Adelson Medical Research Foundation.
Employment or leadership: None declared.
Honorarium: None declared.
Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.
Pertwee RG. Emerging strategies for exploiting cannabinoid receptor agonists as medicines. Br J Pharmacol 2009;156:397–411.
Mechoulam R, Hanuš LO, Pertwee R, Howlett AC. Early phytocannabinoid chemistry to endocannabinoids and beyond. Nat Rev Neurosci 2014;15:757–64.
Izzo AA, Borrelli F, Capasso R, Di Marzo V, Mechoulam R. Non-psychotropic plant cannabinoids: new therapeutic opportunities from an ancient herb. Trends Pharmacol Sci 2009;30:515–27.
Nagarkatti P, Pandey R, Rieder SA, Hegde VL, Nagarkatti M. Cannabinoids as novel anti-inflammatory drugs. Future Med Chem 2009;1:1333–49.
Kozela E, Pietr M, Juknat A, Rimmerman N, Levy R, Vogel Z. Cannabinoids Δ9-tetrahydrocannabinol and cannabidiol differentially inhibit the lipopolysaccharide-activated NF-κB and interferon-β/STAT proinflammatory pathways in BV-2 microglial cells. J Biol Chem 2010;285:1616–26.
- Export Citation
Kozela E, Pietr M, Juknat A, Rimmerman N, Levy R, Vogel Z. Cannabinoids Δ9-tetrahydrocannabinol and cannabidiol differentially inhibit the lipopolysaccharide-activated NF-κB and interferon-β/STAT proinflammatory pathways in BV-2 microglial cells. J Biol Chem 2010;285:1616–26.)| false 10.1074/jbc.M109.069294 19910459
Kozela E, Lev N, Kaushansky N, Eilam R, Rimmerman N, Levy R, et al. Cannabidiol inhibits pathogenic T cells, decreases spinal microglial activation and ameliorates multiple sclerosis-like disease in C57BL/6 mice. Br J Pharmacol 2011;163:1507–19.
- Export Citation
Kozela E, Lev N, Kaushansky N, Eilam R, Rimmerman N, Levy R, et al. Cannabidiol inhibits pathogenic T cells, decreases spinal microglial activation and ameliorates multiple sclerosis-like disease in C57BL/6 mice. Br J Pharmacol 2011;163:1507–19.)| false 10.1111/j.1476-5381.2011.01379.x 21449980
Kozela E, Juknat A, Kaushansky N, Rimmerman N, Ben-Nun A, Vogel Z. Cannabinoids decrease the th17 inflammatory autoimmune phenotype. J Neuroimmune Pharmacol 2013;8:1265–76.
Kozela E, Juknat A, Kaushansky N, Ben-Nun A, Coppola G, Vogel Z. Cannabidiol, a non-psychoactive cannabinoid, leads to EGR2-dependent anergy in activated encephalitogenic T cells. J Neuroinflammation 2015;12:52.
Juknat A, Pietr M, Kozela E, Rimmerman N, Levy R, Coppola G, et al. Differential transcriptional profiles mediated by exposure to the cannabinoids cannabidiol and Δ9-tetrahydrocannabinol in BV-2 microglial cells. Br J Pharmacol 2012;165:2512–28.
- Export Citation
Juknat A, Pietr M, Kozela E, Rimmerman N, Levy R, Coppola G, et al. Differential transcriptional profiles mediated by exposure to the cannabinoids cannabidiol and Δ9-tetrahydrocannabinol in BV-2 microglial cells. Br J Pharmacol 2012;165:2512–28.)| false 10.1111/j.1476-5381.2011.01461.x 21542829
Juknat A, Rimmerman N, Levy R, Vogel Z, Kozela E. Cannabidiol affects the expression of genes involved in zinc homeostasis in BV-2 microglial cells. Neurochem Int 2012;61:923–30.
Juknat A, Pietr M, Kozela E, Rimmerman N, Levy R, Gao F, et al. Microarray and pathway analysis reveal distinct mechanisms underlying cannabinoid-mediated modulation of LPS-induced activation of BV-2 microglial cells. PLoS One 2013;8:e61462.
- Export Citation
Juknat A, Pietr M, Kozela E, Rimmerman N, Levy R, Gao F, et al. Microarray and pathway analysis reveal distinct mechanisms underlying cannabinoid-mediated modulation of LPS-induced activation of BV-2 microglial cells. PLoS One 2013;8:e61462.)| false 10.1371/journal.pone.0061462 23637839
Chiurchiù V, Leuti A, Maccarrone M. Cannabinoid signaling and neuroinflammatory diseases: a melting pot for the regulation of brain immune responses. J Neuroimmune Pharmacol 2015;10:268–80.
Massi P, Valenti M, Solinas M, Parolaro D. Molecular mechanisms involved in the antitumor activity of cannabinoids on gliomas: role for oxidative stress. Cancers 2010;2:1013–26.
Pertwee RG, Howlett AC, Abood ME, Alexander SP, Di Marzo V, Elphick MR, et al. International Union of Basic and Clinical Pharmacology. LXXIX. Cannabinoid receptors and their ligands: beyond CB₁ and CB₂. Pharmacol Rev 2010;62:588–631.
Basu S, Dittel BN. Unraveling the complexities of cannabinoid receptor 2 immune regulation in health and disease. Immunol Res 2011;51:26–38.
Rimmerman N, Kozela E, Levy R, Vogel Z, Juknat A. Cannabinoid signaling through non-CB1R/non-CB2R targets in microglia. In: Abood ME, Sorensen RG, Stella N, editors. Endocannabinoids: actions at non-CB1/CB2 cannabinoid receptors. New York: Springer, 2013:143–71.
- Export Citation
Rimmerman N, Kozela E, Levy R, Vogel Z, Juknat A. Cannabinoid signaling through non-CB1R/non-CB2R targets in microglia. In: Abood ME, Sorensen RG, Stella N, editors. Endocannabinoids: actions at non-CB1/CB2 cannabinoid receptors. New York: Springer, 2013:143–71.)| false 10.1007/978-1-4614-4669-9_7
Xiong W, Cui T, Cheng K, Yang F, Chen SR, Willenbring D, et al. Cannabinoids suppress inflammatory and neuropathic pain by targeting α3 glycine receptors. J Exp Med 2012;209:1121–34.
Kozela E, Haj C, Hanuš L, Shurki A, Chourasia M, Juknat A, et al. HU-446 and HU-465, derivatives of the non-psychoactive cannabinoid cannabidiol, decrease the activation of encephalitogenic T cells. Chem Biol Drug Des 2015. DOI: 10.1111/cbdd.12637 [Epub ahead of print].
- Export Citation
Kozela E, Haj C, Hanuš L, Shurki A, Chourasia M, Juknat A, et al. HU-446 and HU-465, derivatives of the non-psychoactive cannabinoid cannabidiol, decrease the activation of encephalitogenic T cells. Chem Biol Drug Des 2015. DOI: 10.1111/cbdd.12637 [Epub ahead of print].)| false 26259697
Gallily R, Even-Chen T, Katzavian G, Lehmann D, Dagan A, Mechoulam R. γ-Irradiation enhances apoptosis induced by cannabidiol, a non-psychotropic cannabinoid, in cultured HL-60 myeloblastic leukemia cells. Leuk Lymphoma 2003;44:1767–73.
- Export Citation
Gallily R, Even-Chen T, Katzavian G, Lehmann D, Dagan A, Mechoulam R. γ-Irradiation enhances apoptosis induced by cannabidiol, a non-psychotropic cannabinoid, in cultured HL-60 myeloblastic leukemia cells. Leuk Lymphoma 2003;44:1767–73.)| false 10.1080/1042819031000103917 14692532
Ben-Shabat S, Hanuš LO, Katzavian G, Gallily R. New cannabidiol derivatives: synthesis, binding to cannabinoid receptor and evaluation of their anti-inflammatory activity. J Med Chem 2006;49:1113–7.
Baek SH, Srebnik M, Mechoulam R. Borontrifluoride on alumina – a modified Lewis acid reagent. An improved synthesis of cannabidiol. Tetrahedron Lett 1985;26:1083–86.
Kaushansky N, Zhong MC, Kerlero de Rosbo N, Hoeftberger R, Lassmann H, Ben-Nun A. Epitope specificity of autoreactive T and B cells associated with experimental autoimmune encephalomyelitis and optic neuritis induced by oligodendrocyte-specific protein in SJL/J mice. J Immunol 2006;15:7364–76.
Lee J-I, Dominy JE Jr, Sikalidis AK, Hirschberger LL, Wang W, Stipanuk MH. HepG2/C3A cells respond to cysteine deprivation by induction of the amino acid deprivation/integrated stress response pathway. Physiol Genomics 2008;33:218–29.
- Export Citation
Lee J-I, Dominy JE Jr, Sikalidis AK, Hirschberger LL, Wang W, Stipanuk MH. HepG2/C3A cells respond to cysteine deprivation by induction of the amino acid deprivation/integrated stress response pathway. Physiol Genomics 2008;33:218–29.)| false 18285520 10.1152/physiolgenomics.00263.2007
Chaveroux C, Lambert-Langlais S, Cherasse Y, Averous J, Parry L, Carraro V, et al. Molecular mechanisms involved in the adaptation to amino acid limitation in mammals. Biochimie 2010;92:736–45.
Averous J, Lambert-Langlais S, Cherasse Y, Carraro V, Parry L, B’chir W, et al. Amino acid deprivation regulates the stress-inducible gene p8 via the GCN2/ATF4 pathway. Biochem Biophys Res Commun 2011;413:24–29.
Kilberg MS, Balasubramanian M, Fu L, Shan J. The transcription factor network associated with the amino acid response in mammalian cells. Adv Nutr 2012;3:295–306.
Kilberg MS, Pan YX, Chen H, Leung-Pineda V. Nutritional control of gene expression: how mammalian cells respond to amino acid limitation. Annu Rev Nutr 2005;25:59–85.
Jin H-O, Seo S-K, Woo S-H, Choe T-B, Hong S-I, Kim J-I, et al. Nuclear protein 1 induced ATF4 in response to various stressors acts as a positive regulator on the transcriptional activation of ATF4. IUBMB Life 2009;61:1153–8.
Carracedo A, Lorente M, Egia A, Blázquez C, García S, Giroux V, et al. The stress-regulated protein p8 mediates cannabinoid-induced apoptosis of tumor cells. Cancer Cell 2006;9:301–12.
Pellerito O, Calvaruso G, Portanova P, De Blasio A, Santulli A, Vento R, et al. The synthetic cannabinoid WIN 55,212-2 sensitizes hepatocellular carcinoma cells to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis by activating p8/CCAAT/enhancer binding protein homologous protein (CHOP)/death receptor 5 (DR5) axis. Mol Pharmacol 2010;77:854–63.
- Export Citation
Pellerito O, Calvaruso G, Portanova P, De Blasio A, Santulli A, Vento R, et al. The synthetic cannabinoid WIN 55,212-2 sensitizes hepatocellular carcinoma cells to tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis by activating p8/CCAAT/enhancer binding protein homologous protein (CHOP)/death receptor 5 (DR5) axis. Mol Pharmacol 2010;77:854–63.)| false 20159939
Jiang Y-F, Vaccaro MI, Fiedler F, Calvo EL, Iovanna JL. Lipopolysaccharides induce p8 mRNA expression in vivo and in vitro. Biochem Biophys Res Commun 1999;260:686–90.
Sasaki H, Sato H, Kuriyama-Matsumura K, Sato K, Maebara K, Wang H, et al. Electrophile response element-mediated induction of the cystine/glutamate exchange transporter gene expression. J Biol Chem 2002;277:44765–71.
Lewerenz J, Hewet SJ, Huang Y, Kambros M, Gout PW, Kalivas PW, et al. The cystine/glutamate antiporter system xc − in health and disease: from molecular mechanisms to novel therapeutic opportunities. Antioxid Redox Signal 2013;18:522–55.
Ishii T, Mann GE. Redox status in mammalian cells and stem cells during culture in vitro: critical roles of Nrf2 and cystine transporter activity in the maintenance of redox balance. Redox Biology 2014;2:786–94.
Sato H, Fujiwara K, Sagara J, Bannai S. Induction of cystine transport activity in mouse peritoneal macrophages by bacterial lipopolysaccharide. Biochem J 1995;310:547–51.
Rojo AI, McBean G, Cindric M, Egea J, Lopez MG, Rada P, et al. Redox control of microglial function: molecular mechanisms and functional significance. Antioxid Redox Signal 2014;21:1766–801.
Naito Y, Takagi T, Higashimura Y. Heme oxygenase-1 and anti-inflammatory M2 macrophages. Arch Biochem Biophys 2014;564:83–8.
McKallip RJ, Jia W, Schlomer J, Warren JW, Nagarkatti PS, Nagarkatti M. Cannabidiol-induced apoptosis in human leukemia cells: a novel role of cannabidiol in the regulation of p22phox and Nox4 expression. Mol Pharmacol 2006;70: 897–908.
Lee CY, Wey SP, Liao MH, Hsu WL, Wu HY, Jan TR. A comparative study on cannabidiol-induced apoptosis in murine thymocytes and EL-4 thymoma cells. Int Immunopharmacol 2008;8:732–40.
McAllister SD, Soroceanu L, Desprez PY. The antitumor activity of plant-derived non-psychoactive cannabinoids. J Neuroimmune Pharmacol 2015;10:255–67.
Morelli MB, Offidani M, Alesiani F, Discepoli G, Liberati S, Olivieri A, et al. The effects of cannabidiol and its synergism with bortezomib in multiple myeloma cell lines. A role for transient receptor potential vanilloid type-2. Int J Cancer 2014;134:2534–46.
- Export Citation
Morelli MB, Offidani M, Alesiani F, Discepoli G, Liberati S, Olivieri A, et al. The effects of cannabidiol and its synergism with bortezomib in multiple myeloma cell lines. A role for transient receptor potential vanilloid type-2. Int J Cancer 2014;134:2534–46.)| false 24293211 10.1002/ijc.28591
Nabissi M, Morelli MB, Amantini C, Liberati S, Santoni M, Ricci-Vitiani L, et al. Cannabidiol stimulates Aml-1a-dependent glial differentiation and inhibits glioma stem-like cells proliferation by inducing autophagy in a TRPV2-dependent manner. Int J Cancer 2015;137:1855–69.
- Export Citation
Nabissi M, Morelli MB, Amantini C, Liberati S, Santoni M, Ricci-Vitiani L, et al. Cannabidiol stimulates Aml-1a-dependent glial differentiation and inhibits glioma stem-like cells proliferation by inducing autophagy in a TRPV2-dependent manner. Int J Cancer 2015;137:1855–69.)| false 10.1002/ijc.29573
Goncharov I, Weiner L, Vogel Z. Delta9-tetrahydrocannabinol increases C6 glioma cell death produced by oxidative stress. Neuroscience 2005;134:567–74.
Wu HY, Chu RM, Wang CC, Lee CY, Lin SH, Jan TR, et al. Cannabidiol-induced apoptosis in primary lymphocytes is associated with oxidative stress-dependent activation of caspase-8. Toxicol Appl Pharmacol 2008;226:260–70.