Abstract

Cannabinoids, the active components of marijuana and their endogenous counterparts, exert many of their actions on the central nervous system by binding to the CB(1) cannabinoid receptor. Different studies have shown that cannabinoids can protect neural cells from different insults. However, those studies have been performed in neurons, whereas no attention has been focused on glial cells. Here we used the pro-apoptotic lipid ceramide to induce apoptosis in astrocytes, and we studied the protective effect exerted by cannabinoids. Results show the following: (i) cannabinoids rescue primary astrocytes from C(2)-ceramide-induced apoptosis in a dose- and time-dependent manner; (ii) triggering of this anti-apoptotic signal depends on the phosphatidylinositol 3-kinase/protein kinase B pathway; (iii) ERK and its downstream target p90 ribosomal S6 kinase might be also involved in the protective effect of cannabinoids; and (iv) cannabinoids protect astrocytes from the cytotoxic effects of focal C(2)-ceramide administration in vivo. In summary, results show that cannabinoids protect astrocytes from ceramide-induced apoptosis via stimulation of the phosphatidylinositol 3-kinase/protein kinase B pathway. These findings constitute the first evidence for an "astroprotective" role of cannabinoids.

Highlights

  • The effects exerted by marijuana and their derivatives through ⌬9-tetrahydrocannabinol (THC)1 and other cannabinoid constituents have been known for many centuries

  • Results show the following: (i) cannabinoids rescue primary astrocytes from C2-ceramide-induced apoptosis in a doseand time-dependent manner; (ii) triggering of this antiapoptotic signal depends on the phosphatidylinositol 3-kinase/protein kinase B pathway; (iii) extracellular signal-regulated kinase (ERK) and its downstream target p90 ribosomal S6 kinase might be involved in the protective effect of cannabinoids; and (iv) cannabinoids protect astrocytes from the cytotoxic effects of focal C2-ceramide administration in vivo

  • The CB1 receptor is coupled to PI3K/PKB [11] and ERK activation [6], and both signaling routes are essential for neural cell survival [21], their possible involvement in the protection of neural cells by cannabinoids is as yet unknown

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Summary

EXPERIMENTAL PROCEDURES

Materials—The following materials were kindly donated: HU-210 by Dr R. Mechoulam (Hebrew University, Jerusalem, Israel); SR 141716 by Sanofi Synthelabo (Montpelier, France); antibodies against total PKB and RSK and the specific PKB/RSK peptide substrate (cross-tide) by Dr D. Alessi (University of Dundee, Dundee, UK); and wild-type and dominant-negative PKB adenoviral vectors by Dr W. DNA fragmentation and TUNEL staining kits and biotin-16-dUTP were from Roche Molecular Biochemicals; deoxynucleotidyltransferase was from Invitrogen; streptavidin Alexa Fluor 488 was from Molecular Probes (Leiden, The Netherlands); wortmannin, LY 294002, PD 098059, Ro 318220, and C2-ceramide were from Alexis Biochemicals (San Diego, CA); anti-HA antibody was from Roche Molecular Biochemicals; anti-phospho-ERK antibody was from Santa Cruz Biotechnology (Santa Cruz, CA); anti-phospho-PKB Thr-308 and phospho-PKB Ser-473 were from Cell Signaling Technology

Cannabinoids Protect Astrocytes from Apoptosis
RESULTS
DISCUSSION
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