Neurotrophic effects of PACAP in the cerebellar cortex

被引:53
作者
Botia, Beatrice
Basille, Magali
Allais, Aurelie
Raoult, Emilie
Falluel-Morel, Anthony
Galas, Ludovic
Jolivel, Valerie
Wurtz, Olivier
Komuro, Hitoshi
Fournier, Alain
Vaudry, Hubert [1 ]
Burel, Delphine
Gonzalez, Bruno J.
Vaudry, David
机构
[1] INSERM, Int Associated Lab Samuel Champlain, U413, F-75654 Paris 13, France
[2] Univ Rouen, Lab Cellular & Mol Neuroendocrinol, F-76821 Rouen, France
[3] Univ Rouen, European Inst Peptide Res, F-76821 Rouen, France
[4] Cleveland Clin Fdn, Lerner Res Inst, Dept Neurosci, Cleveland, OH 44195 USA
[5] Univ Quebec, Inst Natl Rech Sci Sante, Inst Armand Frappier, Pointe Claire, PQ H9R 1G6, Canada
关键词
cerebellar granule neurons; PACAP; cAMP/PKA; apoptosis; caspase-3; neuroprotection;
D O I
10.1016/j.peptides.2007.04.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the rodent cerebellum, PACAP is expressed by Purkinje neurons and PAC1 receptors are present on granule cells during both the development period and in adulthood. Treatment of granule neurons with PACAP inhibits proliferation, slows migration, promotes survival and induces differentiation. PACAP also protects cerebellar granule cells against the deleterious effects of neurotoxic agents. Most of the neurotrophic effects of PACAP are mediated through the cAMP/PKA signaling pathway and often involve the ERK MAPkinase. Caspase-3 is one of the key enzymes implicated in the neuroprotective action of PACAP but PACAP also inhibits caspase-9 activity and increases Bcl-2 expression. PACAP and functional PAC1 receptors are expressed in the monkey and human cerebellar cortex with a pattern of expression very similar to that described in rodents, suggesting that PACAP could also exert neurodevelopmental and neuroprotective functions in the cerebellum of primates including human. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1746 / 1752
页数:7
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