The HSPG Glypican Regulates Experience-Dependent Synaptic and Behavioral Plasticity by Modulating the Non-Canonical BMP Pathway.

The HSPG Glypican Regulates Experience-Dependent Synaptic and Behavioral Plasticity by Modulating the Non-Canonical BMP Pathway.
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DOI:
10.1016/j.celrep.2019.08.032
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发表时间:
2019-09
期刊:
影响因子:
8.8
通讯作者:
K. Kamimura;Ai Odajima;Yuko Ikegawa;Chikako Maru;N. Maeda
K. Kamimura;Ai Odajima;Yuko Ikegawa;Chikako Maru;N. Maeda
中科院分区:
生物学1区
文献类型:
--
作者:
K. Kamimura;Ai Odajima;Yuko Ikegawa;Chikako Maru;N. Maeda

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Under food deprivation conditions,Drosophilalarvae exhibit increases in locomotor speed and synaptic bouton numbers at neuromuscular junctions (NMJs). Octopamine, the invertebrate counterpart of noradrenaline, plays critical roles in this process; however, the underlying mechanisms remain unclear. We show here that a glypican (Dlp) negatively regulates type I synaptic bouton formation, postsynaptic expression of GluRIIA, and larval locomotor speed. Starvation-induced octopaminergic signaling decreases Dlp expression, leading to increases in synapse formation and locomotion. Dlp is expressed by postsynaptic muscle cells and suppresses the non-canonical BMP pathway, which is composed of the presynaptic BMP receptor Wit and postsynaptic GluRIIA-containing ionotropic glutamate receptor. We find that during starvation, decreases in Dlp increase non-canonical BMP signaling, leading to increases in GluRIIA expression, type I bouton number, and locomotor speed. Our results demonstrate that octopamine controls starvation-induced neural plasticity by regulating Dlp and provides insights into how proteoglycans can influence behavioral and synaptic plasticity.