A Presynaptic Glutamate Receptor Subunit Confers Robustness to Neurotransmission and Homeostatic Potentiation

被引:44
|
作者
Kiragasi, Beril [1 ,2 ]
Wondolowski, Joyce [1 ]
Li, Yan [3 ]
Dickman, Dion K. [1 ]
机构
[1] Univ Southern Calif, Dept Neurobiol, Los Angeles, CA 90089 USA
[2] Univ Southern Calif, USC Neurosci Grad Program, Los Angeles, CA 90089 USA
[3] Eunice Kennedy Shriver Natl Inst Child Hlth & Hum, Sect Neuronal Connect, Lab Gene Regulat & Dev, Bethesda, MD 20892 USA
来源
CELL REPORTS | 2017年 / 19卷 / 13期
关键词
KAINATE RECEPTORS; SYNAPTIC-TRANSMISSION; TRANSMITTER RELEASE; DROSOPHILA LARVAL; CENTRAL NEURONS; MECHANISMS; PLASTICITY; MODULATION; EXPRESSION; REVEALS;
D O I
10.1016/j.celrep.2017.06.003
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Homeostatic signaling systems are thought to interface with other forms of plasticity to ensure flexible yet stable levels of neurotransmission. The role of neurotransmitter receptors in this process, beyond mediating neurotransmission itself, is not known. Through a forward genetic screen, we have identified the Drosophila kainate-type ionotropic glutamate receptor subunit DKaiR1D to be required for the retrograde, homeostatic potentiation of synaptic strength. DKaiR1D is necessary in presynaptic motor neurons, localized near active zones, and confers robustness to the calciumsensitivity of baseline synaptic transmission. Acute pharmacological blockade of DKaiR1D disrupts homeostatic plasticity, indicating that this receptor is required for the expression of this process, distinct from developmental roles. Finally, we demonstrate that calcium permeability through DKaiR1D is necessary for baseline synaptic transmission, but not for homeostatic signaling. We propose that DKaiR1D is a glutamate autoreceptor that promotes robustness to synaptic strength and plasticity with active zone specificity.
引用
收藏
页码:2694 / 2706
页数:13
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