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Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex

The adult brain lacks sensitivity to changes in the sensory environment found in the juvenile brain. The transplantation of embryonic interneurons has been shown to restore juvenile plasticity to the adult host visual cortex. It is unclear whether transplanted interneurons directly mediate the renew...

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Autores principales: Zheng, XiaoTing, Salinas, Kirstie J., Velez, Dario X. Figueroa, Nakayama, Taylor, Lin, Xiaoxiao, Banerjee, Dhruba, Xu, Xiangmin, Gandhi, Sunil P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870960/
https://www.ncbi.nlm.nih.gov/pubmed/33558487
http://dx.doi.org/10.1038/s41467-021-21097-4
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author Zheng, XiaoTing
Salinas, Kirstie J.
Velez, Dario X. Figueroa
Nakayama, Taylor
Lin, Xiaoxiao
Banerjee, Dhruba
Xu, Xiangmin
Gandhi, Sunil P.
author_facet Zheng, XiaoTing
Salinas, Kirstie J.
Velez, Dario X. Figueroa
Nakayama, Taylor
Lin, Xiaoxiao
Banerjee, Dhruba
Xu, Xiangmin
Gandhi, Sunil P.
author_sort Zheng, XiaoTing
collection PubMed
description The adult brain lacks sensitivity to changes in the sensory environment found in the juvenile brain. The transplantation of embryonic interneurons has been shown to restore juvenile plasticity to the adult host visual cortex. It is unclear whether transplanted interneurons directly mediate the renewed cortical plasticity or whether these cells act indirectly by modifying the host interneuron circuitry. Here we find that the transplant-induced reorganization of mouse host circuits is specifically mediated by Neuregulin (NRG1)/ErbB4 signaling in host parvalbumin (PV) interneurons. Brief visual deprivation reduces the visual activity of host PV interneurons but has negligible effects on the responses of transplanted PV interneurons. Exogenous NRG1 both prevents the deprivation-induced reduction in the visual responses of host PV interneurons and blocks the transplant-induced reorganization of the host circuit. While deletion of ErbB4 receptors from host PV interneurons blocks cortical plasticity in the transplant recipients, deletion of the receptors from the donor PV interneurons does not. Altogether, our results indicate that transplanted embryonic interneurons reactivate cortical plasticity by rejuvenating the function of host PV interneurons.
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spelling pubmed-78709602021-02-11 Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex Zheng, XiaoTing Salinas, Kirstie J. Velez, Dario X. Figueroa Nakayama, Taylor Lin, Xiaoxiao Banerjee, Dhruba Xu, Xiangmin Gandhi, Sunil P. Nat Commun Article The adult brain lacks sensitivity to changes in the sensory environment found in the juvenile brain. The transplantation of embryonic interneurons has been shown to restore juvenile plasticity to the adult host visual cortex. It is unclear whether transplanted interneurons directly mediate the renewed cortical plasticity or whether these cells act indirectly by modifying the host interneuron circuitry. Here we find that the transplant-induced reorganization of mouse host circuits is specifically mediated by Neuregulin (NRG1)/ErbB4 signaling in host parvalbumin (PV) interneurons. Brief visual deprivation reduces the visual activity of host PV interneurons but has negligible effects on the responses of transplanted PV interneurons. Exogenous NRG1 both prevents the deprivation-induced reduction in the visual responses of host PV interneurons and blocks the transplant-induced reorganization of the host circuit. While deletion of ErbB4 receptors from host PV interneurons blocks cortical plasticity in the transplant recipients, deletion of the receptors from the donor PV interneurons does not. Altogether, our results indicate that transplanted embryonic interneurons reactivate cortical plasticity by rejuvenating the function of host PV interneurons. Nature Publishing Group UK 2021-02-08 /pmc/articles/PMC7870960/ /pubmed/33558487 http://dx.doi.org/10.1038/s41467-021-21097-4 Text en © The Author(s) 2021 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Zheng, XiaoTing
Salinas, Kirstie J.
Velez, Dario X. Figueroa
Nakayama, Taylor
Lin, Xiaoxiao
Banerjee, Dhruba
Xu, Xiangmin
Gandhi, Sunil P.
Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
title Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
title_full Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
title_fullStr Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
title_full_unstemmed Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
title_short Host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
title_sort host interneurons mediate plasticity reactivated by embryonic inhibitory cell transplantation in mouse visual cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7870960/
https://www.ncbi.nlm.nih.gov/pubmed/33558487
http://dx.doi.org/10.1038/s41467-021-21097-4
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