scholarly journals Higher-order thalamocortical inputs gate synaptic long-term potentiation via disinhibition

2018 ◽  
Author(s):  
Leena E. Williams ◽  
Anthony Holtmaat
Keyword(s):  
Pyramidal Neurons ◽  
Sensory Information ◽  
Long Term Potentiation ◽  
Higher Order ◽  
Synaptic Circuits ◽  
Term Potentiation ◽  
Cortical Pyramidal Neurons ◽  
Whisker Stimulation ◽  
Synaptic Circuitry

SUMMARYSensory experience and perceptual learning changes the receptive field properties of cortical pyramidal neurons, largely mediated by long-term potentiation (LTP) of synapses. The circuit mechanisms underlying cortical LTP remain unclear. In the mouse somatosensory cortex (S1), LTP can be elicited in layer (L) 2/3 pyramidal neurons by rhythmic whisker stimulation. We combined electrophysiology, optogenetics, and chemogenetics in thalamocortical slices to dissect the synaptic circuitry underlying this LTP. We found that projections from higher-order, posteriormedial thalamic complex (POm) to S1 are key to eliciting NMDAR-dependent LTP of intracortical synapses. Paired activation of intracortical and higher-order thalamocortical pathways increased vasoactive intestinal peptide (VIP) interneuron and decreased somatostatin (SST) interneuron activity, which was critical for inducing LTP. Our results reveal a novel circuit motif in which higher-order thalamic feedback gates plasticity of intracortical synapses in S1 via disinhibition. This motif may allow contextual feedback to shape synaptic circuits that process first-order sensory information.

scholarly journals GPR68 deletion impairs hippocampal long-term potentiation and passive avoidance behavior

2020 ◽  
Vol 13 (1) ◽  
Author(s):  
Yuanyuan Xu ◽  
Mike T. Lin ◽  
Xiang-ming Zha
Keyword(s):  
Passive Avoidance ◽  
Pyramidal Neurons ◽  
Granule Cells ◽  
Hippocampal Slices ◽  
Synaptic Cleft ◽  
Long Term Potentiation ◽  
Synaptic Function ◽  
Metabotropic Receptor ◽  
Term Potentiation

Abstract Increased neural activities reduced pH at the synaptic cleft and interstitial spaces. Recent studies have shown that protons function as a neurotransmitter. However, it remains unclear whether protons signal through a metabotropic receptor to regulate synaptic function. Here, we showed that GPR68, a proton-sensitive GPCR, exhibited wide expression in the hippocampus, with higher expression observed in CA3 pyramidal neurons and dentate granule cells. In organotypic hippocampal slice neurons, ectopically expressed GPR68-GFP was present in dendrites, dendritic spines, and axons. Recordings in hippocampal slices isolated from GPR68−/− mice showed a reduced fiber volley at the Schaffer collateral-CA1 synapses, a reduced long-term potentiation (LTP), but unaltered paired-pulse ratio. In a step-through passive avoidance test, GPR68−/− mice exhibited reduced avoidance to the dark chamber. These findings showed that GPR68 contributes to hippocampal LTP and aversive fear memory.

scholarly journals Prolonged development of long-term potentiation at lateral entorhinal cortex synapses onto adult-born neurons

PLoS ONE ◽  
2021 ◽  
Vol 16 (6) ◽  
pp. e0253642
Author(s):  
Nicholas P. Vyleta ◽  
Jason S. Snyder
Keyword(s):  
Entorhinal Cortex ◽  
Critical Period ◽  
Spatial Information ◽  
Dynamic Range ◽  
Sensory Information ◽  
Long Term Potentiation ◽  
Perforant Path ◽  
Term Potentiation ◽  
Adult Born Neurons

Critical period plasticity at adult-born neuron synapses is widely believed to contribute to the learning and memory functions of the hippocampus. Experience regulates circuit integration and for a transient interval, until cells are ~6 weeks old, new neurons display enhanced long-term potentiation (LTP) at afferent and efferent synapses. Since neurogenesis declines substantially with age, this raises questions about the extent of lasting plasticity offered by adult-born neurons. Notably, however, the hippocampus receives sensory information from two major cortical pathways. Broadly speaking, the medial entorhinal cortex conveys spatial information to the hippocampus via the medial perforant path (MPP), and the lateral entorhinal cortex, via the lateral perforant path (LPP), codes for the cues and items that make experiences unique. While enhanced critical period plasticity at MPP synapses is relatively well characterized, no studies have examined long-term plasticity at LPP synapses onto adult-born neurons, even though the lateral entorhinal cortex is uniquely vulnerable to aging and Alzheimer’s pathology. We therefore investigated LTP at LPP inputs both within (4–6 weeks) and beyond (8+ weeks) the traditional critical period. At immature stages, adult-born neurons did not undergo significant LTP at LPP synapses, and often displayed long-term depression after theta burst stimulation. However, over the course of 3–4 months, adult-born neurons displayed increasingly greater amounts of LTP. Analyses of short-term plasticity point towards a presynaptic mechanism, where transmitter release probability declines as cells mature, providing a greater dynamic range for strengthening synapses. Collectively, our findings identify a novel form of new neuron plasticity that develops over an extended interval, and may therefore be relevant for maintaining cognitive function in aging.

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