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Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus
Axons of retinal ganglion cells (RGCs) play critical roles in the development of inhibitory circuits in visual thalamus. We previously reported that RGC axons signal astrocytes to induce the expression of fibroblast growth factor 15 (FGF15), a motogen required for GABAergic interneuron migration int...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640189/ https://www.ncbi.nlm.nih.gov/pubmed/36342840 http://dx.doi.org/10.7554/eLife.79833 |
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author | Somaiya, Rachana Deven Stebbins, Katelyn Gingrich, Ellen C Xie, Hehuang Campbell, John N Garcia, A Denise R Fox, Michael A |
author_facet | Somaiya, Rachana Deven Stebbins, Katelyn Gingrich, Ellen C Xie, Hehuang Campbell, John N Garcia, A Denise R Fox, Michael A |
author_sort | Somaiya, Rachana Deven |
collection | PubMed |
description | Axons of retinal ganglion cells (RGCs) play critical roles in the development of inhibitory circuits in visual thalamus. We previously reported that RGC axons signal astrocytes to induce the expression of fibroblast growth factor 15 (FGF15), a motogen required for GABAergic interneuron migration into visual thalamus. However, how retinal axons induce thalamic astrocytes to generate Fgf15 and influence interneuron migration remains unknown. Here, we demonstrate that impairing RGC activity had little impact on interneuron recruitment into mouse visual thalamus. Instead, our data show that retinal-derived sonic hedgehog (SHH) is essential for interneuron recruitment. Specifically, we show that thalamus-projecting RGCs express SHH and thalamic astrocytes generate downstream components of SHH signaling. Deletion of RGC-derived SHH leads to a significant decrease in Fgf15 expression, as well as in the percentage of interneurons recruited into visual thalamus. Overall, our findings identify a morphogen-dependent neuron–astrocyte signaling mechanism essential for the migration of thalamic interneurons. |
format | Online Article Text |
id | pubmed-9640189 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-96401892022-11-08 Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus Somaiya, Rachana Deven Stebbins, Katelyn Gingrich, Ellen C Xie, Hehuang Campbell, John N Garcia, A Denise R Fox, Michael A eLife Neuroscience Axons of retinal ganglion cells (RGCs) play critical roles in the development of inhibitory circuits in visual thalamus. We previously reported that RGC axons signal astrocytes to induce the expression of fibroblast growth factor 15 (FGF15), a motogen required for GABAergic interneuron migration into visual thalamus. However, how retinal axons induce thalamic astrocytes to generate Fgf15 and influence interneuron migration remains unknown. Here, we demonstrate that impairing RGC activity had little impact on interneuron recruitment into mouse visual thalamus. Instead, our data show that retinal-derived sonic hedgehog (SHH) is essential for interneuron recruitment. Specifically, we show that thalamus-projecting RGCs express SHH and thalamic astrocytes generate downstream components of SHH signaling. Deletion of RGC-derived SHH leads to a significant decrease in Fgf15 expression, as well as in the percentage of interneurons recruited into visual thalamus. Overall, our findings identify a morphogen-dependent neuron–astrocyte signaling mechanism essential for the migration of thalamic interneurons. eLife Sciences Publications, Ltd 2022-11-07 /pmc/articles/PMC9640189/ /pubmed/36342840 http://dx.doi.org/10.7554/eLife.79833 Text en © 2022, Somaiya et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Somaiya, Rachana Deven Stebbins, Katelyn Gingrich, Ellen C Xie, Hehuang Campbell, John N Garcia, A Denise R Fox, Michael A Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus |
title | Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus |
title_full | Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus |
title_fullStr | Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus |
title_full_unstemmed | Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus |
title_short | Sonic hedgehog-dependent recruitment of GABAergic interneurons into the developing visual thalamus |
title_sort | sonic hedgehog-dependent recruitment of gabaergic interneurons into the developing visual thalamus |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9640189/ https://www.ncbi.nlm.nih.gov/pubmed/36342840 http://dx.doi.org/10.7554/eLife.79833 |
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