A Unique Homeostatic Signaling Pathway Links Synaptic Inactivity to Postsynaptic mTORC1
| Autor: | Fredrick E. Henry, Michael A. Sutton, Cynthia J. L. Carruthers, Amanda S. Perez, Xiao Wang, Edward L. Stuenkel, David Serrano |
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| Rok vydání: | 2018 |
| Předmět: |
Male
0301 basic medicine Long-Term Potentiation Mechanistic Target of Rapamycin Complex 1 Biology Hippocampus Rats Sprague-Dawley 03 medical and health sciences Postsynaptic potential Homeostatic plasticity Animals Homeostasis Long-term depression Research Articles PI3K/AKT/mTOR pathway Neurons General Neuroscience Long-term potentiation Rats 030104 developmental biology Synapses Synaptic plasticity Retrograde signaling Excitatory postsynaptic potential Female biological phenomena cell phenomena and immunity Neuroscience Signal Transduction |
| Zdroj: | The Journal of Neuroscience. 38:2207-2225 |
| ISSN: | 1529-2401 0270-6474 |
| DOI: | 10.1523/jneurosci.1843-17.2017 |
| Popis: | mTORC1-dependent translational control plays a key role in several enduring forms of synaptic plasticity such as long term potentiation (LTP) and mGluR-dependent long term depression. Recent evidence demonstrates an additional role in regulating synaptic homeostasis in response to inactivity, where dendritic mTORC1 serves to modulate presynaptic function via retrograde signaling. Presently, it is unclear whether LTP and homeostatic plasticity use a common route to mTORC1-dependent signaling or whether each engage mTORC1 through distinct pathways. Here, we report a unique signaling pathway that specifically couples homeostatic signaling to postsynaptic mTORC1 after loss of excitatory synaptic input. We find that AMPAR blockade, but not LTP-inducing stimulation, induces phospholipase D (PLD)-dependent synthesis of the lipid second messenger phosphatidic acid (PA) in rat cultured hippocampal neurons of either sex. Pharmacological blockade of PLD1/2 or pharmacogenetic disruption of PA interactions with mTOR eliminates mTORC1 signaling and presynaptic compensation driven by AMPAR blockade, but does not alter mTORC1 activation or functional changes during chemical LTP (cLTP). Overexpression of PLD1, but not PLD2, recapitulates both functional synaptic changes as well as signature cellular adaptations associated with homeostatic plasticity. Finally, transient application of exogenous PA is sufficient to drive rapid presynaptic compensation requiring mTORC1-dependent translation of BDNF in the postsynaptic compartment. These results thus define a unique homeostatic signaling pathway coupling mTORC1 activation to changes in excitatory synaptic drive. Our results further imply that more than one canonical mTORC1 activation pathway may be relevant for the design of novel therapeutic approaches against neurodevelopmental disorders associated with mTORC1 dysregulation.SIGNIFICANCE STATEMENTHomeostatic and Hebbian forms of synaptic plasticity are thought to play complementary roles in regulating neural circuit function, but we know little about how these forms of plasticity are distinguished at the single neuron level. Here, we define a signaling pathway that uniquely links mTORC1 with homeostatic signaling in neurons. |
| Databáze: | OpenAIRE |
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