Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Somaiya, Rachana Deven, Stebbins, Katelyn, Gingrich, Ellen C, Xie, Hehuang, Campbell, John N, Garcia, A Denise R, Fox, Michael A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
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
_version_ 1784825795248652288
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
work_keys_str_mv AT somaiyarachanadeven sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus
AT stebbinskatelyn sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus
AT gingrichellenc sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus
AT xiehehuang sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus
AT campbelljohnn sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus
AT garciaadeniser sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus
AT foxmichaela sonichedgehogdependentrecruitmentofgabaergicinterneuronsintothedevelopingvisualthalamus