D. Vaudry and A. Falluel-Morel contributed equally to this work.
Pituitary adenylate cyclase-activating polypeptide prevents C2-ceramide-induced apoptosis of cerebellar granule cells
Article first published online: 17 MAR 2003
Copyright © 2003 Wiley-Liss, Inc.
Journal of Neuroscience Research
Volume 72, Issue 3, pages 303–316, 1 May 2003
How to Cite
Vaudry, D., Falluel-Morel, A., Basille, M., Pamantung, T. F., Fontaine, M., Fournier, A., Vaudry, H. and Gonzalez, B. J. (2003), Pituitary adenylate cyclase-activating polypeptide prevents C2-ceramide-induced apoptosis of cerebellar granule cells. J. Neurosci. Res., 72: 303–316. doi: 10.1002/jnr.10530
- Issue published online: 7 APR 2003
- Article first published online: 17 MAR 2003
- Manuscript Accepted: 21 OCT 2002
- Manuscript Revised: 14 OCT 2002
- Manuscript Received: 29 MAR 2002
- INSERM. Grant Number: U413
- IREB. Grant Number: 2001/22
- Conseil Régional de Haute-Normandie. Grant Number: LARC-Neuroscience program
The sphingolipid metabolites, ceramides, are critical mediators of the cellular stress response and play an important role in the control of programmed cell death. In particular, ceramides have been shown to induce apoptosis of cerebellar granule cells. We show that pituitary adenylate cyclase-activating polypeptide (PACAP) prevents C2-ceramide-induced apoptosis. The neuroprotective effect of PACAP was dose-dependent and blocked by its antagonist, PACAP6-38, whereas the PACAP-related peptide VIP was inactive. The effect of PACAP on cell survival was mimicked by dibutyryl-cAMP (dbcAMP) and forskolin and prevented by the MEK inhibitor U0126, indicating that both the adenylyl-cyclase and MAP-kinase pathways contribute to the neuroprotective action of the peptide. C2-ceramide and PACAP induced opposite effects on phosphorylated forms of ERK and JNK without affecting the total amounts of ERK and JNK, suggesting that a balance between these two MAP-kinases is critical for the cell survival/death decision. The effect of PACAP on ERK phosphorylation was blocked by U0126, but was not affected by H89 or chelerythrine indicating that PACAP activates ERK through a PKA- and PKC-independent mechanism. C2-ceramide induced a time-dependent activation of caspase-3, enhanced the amount of cleaved caspase-3 and stimulated the DNA fragmentation process, while PACAP strongly inhibited the C2-ceramide-induced activation of caspase-3, reduced the expression of cleaved caspase-3 and blocked DNA fragmentation. Taken together, the present results show that C2-ceramide induces apoptosis of cerebellar granule cells through a mechanism involving activation of caspase-3. Our data also demonstrate that PACAP is a potent inhibitor of C2-ceramide-induced apoptosis. © 2003 Wiley-Liss, Inc.