The Gαo Activator Mastoparan-7 Promotes Dendritic Spine Formation in Hippocampal Neurons

被引:10
|
作者
Ramirez, Valerie T. [1 ]
Ramos-Fernandez, Eva [1 ]
Inestrosa, Nibaldo C. [1 ,2 ,3 ,4 ]
机构
[1] Pontificia Univ Catolica Chile, Fac Ciencias Biol, Ctr Envejecimiento & Regenerac CARE, Santiago 8331150, Chile
[2] Univ New S Wales, Fac Med, Sch Psychiat, Ctr Hlth Brain Ageing, Sydney, NSW, Australia
[3] Pontificia Univ Catolica Chile, Ctr UC Sindrome Down, Santiago 8331150, Chile
[4] Univ Magallanes, Ctr Excelencia Biomed Magallanes CEBIMA, Punta Arenas, Chile
关键词
HETEROTRIMERIC G-PROTEINS; WASP VENOM; PEPTIDE; PSD-95; MECHANISMS; PLASTICITY; APOPTOSIS; RECEPTOR; CALCIUM; CAMKII;
D O I
10.1155/2016/4258171
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mastoparan-7 (Mas-7), an analogue of the peptide mastoparan, which is derived from wasp venom, is a direct activator of Pertussis toxin-(PTX-) sensitive G proteins. Mas-7 produces several biological effects in different cell types; however, little is known about howMas-7 influences mature hippocampal neurons. We examined the specific role of Mas-7 in the development of dendritic spines, the sites of excitatory synaptic contact that are crucial for synaptic plasticity. We report here that exposure of hippocampal neurons to a low dose of Mas-7 increases dendritic spine density and spine head width in a time-dependent manner. Additionally, Mas-7 enhances postsynaptic density protein-95 (PSD-95) clustering in neurites and activates G alpha(o) signaling, increasing the intracellular Ca2+ concentration. To define the role of signaling intermediates, we measured the levels of phosphorylated protein kinase C (PKC), c-Jun N-terminal kinase (JNK), and calcium-calmodulin dependent protein kinase II alpha (CaMKII alpha) after Mas-7 treatment and determined that CaMKII activation is necessary for the Mas-7-dependent increase in dendritic spine density. Our results demonstrate a critical role for G alpha(o) subunit signaling in the regulation of synapse formation.
引用
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页数:11
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