Cargando…
Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex
At glutamatergic synapses, astrocytes respond to the neurotransmitter glutamate with intracellular Ca(2+) elevations and the release of gliotransmitters that modulate synaptic transmission. While the functional interactions between neurons and astrocytes have been intensively studied at glutamatergi...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102536/ https://www.ncbi.nlm.nih.gov/pubmed/35563706 http://dx.doi.org/10.3390/cells11091400 |
_version_ | 1784707352419631104 |
---|---|
author | Henriques, Vanessa Jorge Chiavegato, Angela Carmignoto, Giorgio Gómez-Gonzalo, Marta |
author_facet | Henriques, Vanessa Jorge Chiavegato, Angela Carmignoto, Giorgio Gómez-Gonzalo, Marta |
author_sort | Henriques, Vanessa Jorge |
collection | PubMed |
description | At glutamatergic synapses, astrocytes respond to the neurotransmitter glutamate with intracellular Ca(2+) elevations and the release of gliotransmitters that modulate synaptic transmission. While the functional interactions between neurons and astrocytes have been intensively studied at glutamatergic synapses, the role of astrocytes at GABAergic synapses has been less investigated. In the present study, we combine optogenetics with 2-photon Ca(2+) imaging experiments and patch-clamp recording techniques to investigate the signaling between Somatostatin (SST)-releasing GABAergic interneurons and astrocytes in brain slice preparations from the visual cortex (VCx). We found that an intense stimulation of SST interneurons evokes Ca(2+) elevations in astrocytes that fundamentally depend on GABA(B) receptor (GABA(B)R) activation, and that this astrocyte response is modulated by the neuropeptide somatostatin. After episodes of SST interneuron hyperactivity, we also observed a long-lasting reduction of the inhibitory postsynaptic current (IPSC) amplitude onto pyramidal neurons (PNs). This reduction of inhibitory tone (i.e., disinhibition) is counterbalanced by the activation of astrocytes that upregulate SST interneuron-evoked IPSC amplitude by releasing ATP that, after conversion to adenosine, activates A(1)Rs. Our results describe a hitherto unidentified modulatory mechanism of inhibitory transmission to VCx layer II/III PNs that involves the functional recruitment of astrocytes by SST interneuron signaling. |
format | Online Article Text |
id | pubmed-9102536 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91025362022-05-14 Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex Henriques, Vanessa Jorge Chiavegato, Angela Carmignoto, Giorgio Gómez-Gonzalo, Marta Cells Article At glutamatergic synapses, astrocytes respond to the neurotransmitter glutamate with intracellular Ca(2+) elevations and the release of gliotransmitters that modulate synaptic transmission. While the functional interactions between neurons and astrocytes have been intensively studied at glutamatergic synapses, the role of astrocytes at GABAergic synapses has been less investigated. In the present study, we combine optogenetics with 2-photon Ca(2+) imaging experiments and patch-clamp recording techniques to investigate the signaling between Somatostatin (SST)-releasing GABAergic interneurons and astrocytes in brain slice preparations from the visual cortex (VCx). We found that an intense stimulation of SST interneurons evokes Ca(2+) elevations in astrocytes that fundamentally depend on GABA(B) receptor (GABA(B)R) activation, and that this astrocyte response is modulated by the neuropeptide somatostatin. After episodes of SST interneuron hyperactivity, we also observed a long-lasting reduction of the inhibitory postsynaptic current (IPSC) amplitude onto pyramidal neurons (PNs). This reduction of inhibitory tone (i.e., disinhibition) is counterbalanced by the activation of astrocytes that upregulate SST interneuron-evoked IPSC amplitude by releasing ATP that, after conversion to adenosine, activates A(1)Rs. Our results describe a hitherto unidentified modulatory mechanism of inhibitory transmission to VCx layer II/III PNs that involves the functional recruitment of astrocytes by SST interneuron signaling. MDPI 2022-04-20 /pmc/articles/PMC9102536/ /pubmed/35563706 http://dx.doi.org/10.3390/cells11091400 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Henriques, Vanessa Jorge Chiavegato, Angela Carmignoto, Giorgio Gómez-Gonzalo, Marta Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex |
title | Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex |
title_full | Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex |
title_fullStr | Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex |
title_full_unstemmed | Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex |
title_short | Astrocytes Modulate Somatostatin Interneuron Signaling in the Visual Cortex |
title_sort | astrocytes modulate somatostatin interneuron signaling in the visual cortex |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9102536/ https://www.ncbi.nlm.nih.gov/pubmed/35563706 http://dx.doi.org/10.3390/cells11091400 |
work_keys_str_mv | AT henriquesvanessajorge astrocytesmodulatesomatostatininterneuronsignalinginthevisualcortex AT chiavegatoangela astrocytesmodulatesomatostatininterneuronsignalinginthevisualcortex AT carmignotogiorgio astrocytesmodulatesomatostatininterneuronsignalinginthevisualcortex AT gomezgonzalomarta astrocytesmodulatesomatostatininterneuronsignalinginthevisualcortex |