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Reciprocal Homosynaptic and heterosynaptic long-term plasticity of corticogeniculate projection neurons in layer VI of the mouse visual cortex.
- Source :
-
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2013 May 01; Vol. 33 (18), pp. 7787-98. - Publication Year :
- 2013
-
Abstract
- Most neurons in layer VI of the visual cortex project to the dorsal lateral geniculate nucleus (dLGN). These corticogeniculate projection neurons (CG cells) receive top-down synaptic inputs from upper layers (ULs) and bottom-up inputs from the underlying white matter (WM). Use-dependent plasticity of these synapses in layer VI of the cortex has received less attention than in other layers. In the present study, we used a retrograde tracer injected into dLGN to identify CG cells, and, by analyzing EPSPs evoked by electrical stimulation of the UL or WM site, examined whether these synapses show long-term synaptic plasticity. Theta-burst stimulation induced long-term potentiation (LTP) of activated synapses (hom-LTP) and long-term depression (LTD) of nonactivated synapses (het-LTD) in either pathway. The paired-pulse stimulation protocol and the analysis of coefficient variation of EPSPs suggested postsynaptic induction of these changes except UL-induced het-LTD, which may be presynaptic in origin. Intracellular injection of a Ca(2+)-chelator suggested an involvement of postsynaptic Ca(2+) rise in all types of long-term plasticity. Pharmacological analysis indicated that NMDA receptors and type-5 metabotropic glutamate receptors are involved in WM-induced and UL-induced plasticity, respectively. Analysis with inhibitors and/or in transgenic mice suggested an involvement of cannabinoid type 1 receptors and calcineurin in UL-induced and WM-induced het-LTD, respectively. These results suggest that hom-LTP and het-LTD may play a role in switching the top-down or bottom-up regulation of CG cell function and/or in maintaining stability of synaptic transmission efficacy through different molecular mechanisms.
- Subjects :
- Animals
Animals, Newborn
Chelating Agents pharmacology
Cholera Toxin metabolism
Electric Stimulation
Excitatory Amino Acid Agents pharmacology
Female
Geniculate Bodies physiology
Glutamate Decarboxylase genetics
Green Fluorescent Proteins genetics
Green Fluorescent Proteins metabolism
In Vitro Techniques
Long-Term Potentiation drug effects
Long-Term Potentiation genetics
Long-Term Synaptic Depression drug effects
Long-Term Synaptic Depression genetics
Male
Mice
Mice, Transgenic
Neurons drug effects
Patch-Clamp Techniques
Receptor, Cannabinoid, CB1 agonists
Receptor, Cannabinoid, CB1 antagonists & inhibitors
Receptor, Cannabinoid, CB1 deficiency
Receptor, Cannabinoid, CB1 genetics
Vesicular Inhibitory Amino Acid Transport Proteins genetics
Visual Pathways physiology
Geniculate Bodies cytology
Long-Term Potentiation physiology
Long-Term Synaptic Depression physiology
Neurons physiology
Visual Cortex cytology
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2401
- Volume :
- 33
- Issue :
- 18
- Database :
- MEDLINE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 23637171
- Full Text :
- https://doi.org/10.1523/JNEUROSCI.5350-12.2013