Profilin2 contributes to synaptic vesicle exocytosis, neuronal excitability, and novelty-seeking behavior

被引:110
作者
Boyl, Pietro Pilo
Di Nardo, Alessia
Mulle, Christophe
Sassoe-Pognetto, Marco
Panzanelli, Patrizia
Mele, Andrea
Kneussel, Matthias
Costantini, Vivian
Perlas, Emerald
Massimi, Marzia
Vara, Hugo
Giustetto, Maurizio
Witke, Walter
机构
[1] EMBL, Mouse Biol Unit, I-00015 Monterotondo, Italy
[2] Childrens Hosp, Dept Neurol, Boston, MA 02115 USA
[3] CNRS, UMR 5091, Inst Francois Magendie, Bordeaux, France
[4] Univ Turin, Dept Anat Pharmacol & Forens Med, Turin, Italy
[5] Univ Turin, Ist Nazl Neurosci, Turin, Italy
[6] Univ Roma La Sapienza, Lab Psicobiol, Dipart Genet & Biol Mol, Rome, Italy
[7] Univ Hamburg, Ctr Mol Neurobiol, ZMNH, Hamburg, Germany
关键词
actin binding proteins; neurotransmitter release; profilin2; synaptic actin polymerization;
D O I
10.1038/sj.emboj.7601737
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
Profilins are actin binding proteins essential for regulating cytoskeletal dynamics, however, their function in the mammalian nervous system is unknown. Here, we provide evidence that in mouse brain profilin1 and profilin2 have distinct roles in regulating synaptic actin polymerization with profilin2 preferring a WAVE-complex-mediated pathway. Mice lacking profilin2 show a block in synaptic actin polymerization in response to depolarization, which is accompanied by increased synaptic excitability of glutamatergic neurons due to higher vesicle exocytosis. These alterations in neurotransmitter release correlate with a hyperactivation of the striatum and enhanced novelty-seeking behavior in profilin2 mutant mice. Our results highlight a novel, profilin2-dependent pathway, regulating synaptic physiology, neuronal excitability, and complex behavior.
引用
收藏
页码:2991 / 3002
页数:12
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