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Astrocytes detect and upregulate transmission at inhibitory synapses of somatostatin interneurons onto pyramidal cells

Astrocytes are important regulators of excitatory synaptic networks. However, astrocytes regulation of inhibitory synaptic systems remains ill defined. This is particularly relevant since GABAergic interneurons regulate the activity of excitatory cells and shape network function. To address this iss...

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Detalles Bibliográficos
Autores principales: Matos, Marco, Bosson, Anthony, Riebe, Ilse, Reynell, Clare, Vallée, Joanne, Laplante, Isabel, Panatier, Aude, Robitaille, Richard, Lacaille, Jean-Claude
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6185912/
https://www.ncbi.nlm.nih.gov/pubmed/30315174
http://dx.doi.org/10.1038/s41467-018-06731-y
Descripción
Sumario:Astrocytes are important regulators of excitatory synaptic networks. However, astrocytes regulation of inhibitory synaptic systems remains ill defined. This is particularly relevant since GABAergic interneurons regulate the activity of excitatory cells and shape network function. To address this issue, we combined optogenetics and pharmacological approaches, two-photon confocal imaging and whole-cell recordings to specifically activate hippocampal somatostatin or paravalbumin-expressing interneurons (SOM-INs or PV-INs), while monitoring inhibitory synaptic currents in pyramidal cells and Ca(2+) responses in astrocytes. We found that astrocytes detect SOM-IN synaptic activity via GABA(B)R and GAT-3-dependent Ca(2+) signaling mechanisms, the latter triggering the release of ATP. In turn, ATP is converted into adenosine, activating A(1)Rs and upregulating SOM-IN synaptic inhibition of pyramidal cells, but not PV-IN inhibition. Our findings uncover functional interactions between a specific subpopulation of interneurons, astrocytes and pyramidal cells, involved in positive feedback autoregulation of dendritic inhibition of pyramidal cells.