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Lamina‐specific properties of spinal astrocytes

Astrocytes are indispensable for proper neuronal functioning. Given the diverse needs of neuronal circuits and the variety of tasks astrocytes perform, the perceived homogeneous nature of astrocytes has been questioned. In the spinal dorsal horn, complex neuronal circuitries regulate the integration...

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Autores principales: Kronschläger, Mira T., Siegert, Anna S. M., Resch, Felix J., Rajendran, Pradeep S., Khakh, Baljit S., Sandkühler, Jürgen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252791/
https://www.ncbi.nlm.nih.gov/pubmed/33694249
http://dx.doi.org/10.1002/glia.23990
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author Kronschläger, Mira T.
Siegert, Anna S. M.
Resch, Felix J.
Rajendran, Pradeep S.
Khakh, Baljit S.
Sandkühler, Jürgen
author_facet Kronschläger, Mira T.
Siegert, Anna S. M.
Resch, Felix J.
Rajendran, Pradeep S.
Khakh, Baljit S.
Sandkühler, Jürgen
author_sort Kronschläger, Mira T.
collection PubMed
description Astrocytes are indispensable for proper neuronal functioning. Given the diverse needs of neuronal circuits and the variety of tasks astrocytes perform, the perceived homogeneous nature of astrocytes has been questioned. In the spinal dorsal horn, complex neuronal circuitries regulate the integration of sensory information of different modalities. The dorsal horn is organized in a distinct laminar manner based on termination patterns of high‐ and low‐threshold afferent fibers and neuronal properties. Neurons in laminae I (L1) and II (L2) integrate potentially painful, nociceptive information, whereas neurons in lamina III (L3) and deeper laminae integrate innocuous, tactile information from the periphery. Sensory information is also integrated by an uncharacterized network of astrocytes. How these lamina‐specific characteristics of neuronal circuits of the dorsal horn are of functional importance for properties of astrocytes is currently unknown. We addressed if astrocytes in L1, L2, and L3 of the upper dorsal horn of mice are differentially equipped for the needs of neuronal circuits that process sensory information of different modalities. We found that astrocytes in L1 and L2 were characterized by a higher density, higher expression of GFAP, Cx43, and GLAST and a faster coupling speed than astrocytes located in L3. L1 astrocytes were more responsive to Kir4.1 blockade and had higher levels of AQP4 compared to L3 astrocytes. In contrast, basic membrane properties, network formation, and somatic intracellular calcium signaling were similar in L1–L3 astrocytes. Our data indicate that the properties of spinal astrocytes are fine‐tuned for the integration of nociceptive versus tactile information.
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spelling pubmed-82527912021-07-12 Lamina‐specific properties of spinal astrocytes Kronschläger, Mira T. Siegert, Anna S. M. Resch, Felix J. Rajendran, Pradeep S. Khakh, Baljit S. Sandkühler, Jürgen Glia Research Articles Astrocytes are indispensable for proper neuronal functioning. Given the diverse needs of neuronal circuits and the variety of tasks astrocytes perform, the perceived homogeneous nature of astrocytes has been questioned. In the spinal dorsal horn, complex neuronal circuitries regulate the integration of sensory information of different modalities. The dorsal horn is organized in a distinct laminar manner based on termination patterns of high‐ and low‐threshold afferent fibers and neuronal properties. Neurons in laminae I (L1) and II (L2) integrate potentially painful, nociceptive information, whereas neurons in lamina III (L3) and deeper laminae integrate innocuous, tactile information from the periphery. Sensory information is also integrated by an uncharacterized network of astrocytes. How these lamina‐specific characteristics of neuronal circuits of the dorsal horn are of functional importance for properties of astrocytes is currently unknown. We addressed if astrocytes in L1, L2, and L3 of the upper dorsal horn of mice are differentially equipped for the needs of neuronal circuits that process sensory information of different modalities. We found that astrocytes in L1 and L2 were characterized by a higher density, higher expression of GFAP, Cx43, and GLAST and a faster coupling speed than astrocytes located in L3. L1 astrocytes were more responsive to Kir4.1 blockade and had higher levels of AQP4 compared to L3 astrocytes. In contrast, basic membrane properties, network formation, and somatic intracellular calcium signaling were similar in L1–L3 astrocytes. Our data indicate that the properties of spinal astrocytes are fine‐tuned for the integration of nociceptive versus tactile information. John Wiley & Sons, Inc. 2021-03-10 2021-07 /pmc/articles/PMC8252791/ /pubmed/33694249 http://dx.doi.org/10.1002/glia.23990 Text en © 2021 The Authors. GLIA published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Kronschläger, Mira T.
Siegert, Anna S. M.
Resch, Felix J.
Rajendran, Pradeep S.
Khakh, Baljit S.
Sandkühler, Jürgen
Lamina‐specific properties of spinal astrocytes
title Lamina‐specific properties of spinal astrocytes
title_full Lamina‐specific properties of spinal astrocytes
title_fullStr Lamina‐specific properties of spinal astrocytes
title_full_unstemmed Lamina‐specific properties of spinal astrocytes
title_short Lamina‐specific properties of spinal astrocytes
title_sort lamina‐specific properties of spinal astrocytes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8252791/
https://www.ncbi.nlm.nih.gov/pubmed/33694249
http://dx.doi.org/10.1002/glia.23990
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