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Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development
Neuron-glia interactions play a critical role in the regulation of synapse formation and circuit assembly. Here we demonstrate that canonical Sonic hedgehog (Shh) pathway signaling in cortical astrocytes acts to coordinate layer-specific synaptic connectivity. We show that the Shh receptor Ptch1 is...
Autores principales: | , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962654/ https://www.ncbi.nlm.nih.gov/pubmed/35196485 http://dx.doi.org/10.1016/j.celrep.2022.110416 |
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author | Xie, Yajun Kuan, Aaron T. Wang, Wengang Herbert, Zachary T. Mosto, Olivia Olukoya, Olubusola Adam, Manal Vu, Steve Kim, Minsu Tran, Diana Gómez, Nicolás Charpentier, Claire Sorour, Ingie Lacey, Tiara E. Tolstorukov, Michael Y. Sabatini, Bernardo L. Lee, Wei-Chung Allen Harwell, Corey C. |
author_facet | Xie, Yajun Kuan, Aaron T. Wang, Wengang Herbert, Zachary T. Mosto, Olivia Olukoya, Olubusola Adam, Manal Vu, Steve Kim, Minsu Tran, Diana Gómez, Nicolás Charpentier, Claire Sorour, Ingie Lacey, Tiara E. Tolstorukov, Michael Y. Sabatini, Bernardo L. Lee, Wei-Chung Allen Harwell, Corey C. |
author_sort | Xie, Yajun |
collection | PubMed |
description | Neuron-glia interactions play a critical role in the regulation of synapse formation and circuit assembly. Here we demonstrate that canonical Sonic hedgehog (Shh) pathway signaling in cortical astrocytes acts to coordinate layer-specific synaptic connectivity. We show that the Shh receptor Ptch1 is expressed by cortical astrocytes during development and that Shh signaling is necessary and sufficient to promote the expression of genes involved in regulating synaptic development and layer-enriched astrocyte molecular identity. Loss of Shh in layer V neurons reduces astrocyte complexity and coverage by astrocytic processes in tripartite synapses; conversely, cell-autonomous activation of Shh signaling in astrocytes promotes cortical excitatory synapse formation. Furthermore, Shh-dependent genes Lrig1 and Sparc distinctively contribute to astrocyte morphology and synapse formation. Together, these results suggest that Shh secreted from deep-layer cortical neurons acts to specialize the molecular and functional features of astrocytes during development to shape circuit assembly and function. |
format | Online Article Text |
id | pubmed-8962654 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
record_format | MEDLINE/PubMed |
spelling | pubmed-89626542022-03-29 Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development Xie, Yajun Kuan, Aaron T. Wang, Wengang Herbert, Zachary T. Mosto, Olivia Olukoya, Olubusola Adam, Manal Vu, Steve Kim, Minsu Tran, Diana Gómez, Nicolás Charpentier, Claire Sorour, Ingie Lacey, Tiara E. Tolstorukov, Michael Y. Sabatini, Bernardo L. Lee, Wei-Chung Allen Harwell, Corey C. Cell Rep Article Neuron-glia interactions play a critical role in the regulation of synapse formation and circuit assembly. Here we demonstrate that canonical Sonic hedgehog (Shh) pathway signaling in cortical astrocytes acts to coordinate layer-specific synaptic connectivity. We show that the Shh receptor Ptch1 is expressed by cortical astrocytes during development and that Shh signaling is necessary and sufficient to promote the expression of genes involved in regulating synaptic development and layer-enriched astrocyte molecular identity. Loss of Shh in layer V neurons reduces astrocyte complexity and coverage by astrocytic processes in tripartite synapses; conversely, cell-autonomous activation of Shh signaling in astrocytes promotes cortical excitatory synapse formation. Furthermore, Shh-dependent genes Lrig1 and Sparc distinctively contribute to astrocyte morphology and synapse formation. Together, these results suggest that Shh secreted from deep-layer cortical neurons acts to specialize the molecular and functional features of astrocytes during development to shape circuit assembly and function. 2022-02-22 /pmc/articles/PMC8962654/ /pubmed/35196485 http://dx.doi.org/10.1016/j.celrep.2022.110416 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ). |
spellingShingle | Article Xie, Yajun Kuan, Aaron T. Wang, Wengang Herbert, Zachary T. Mosto, Olivia Olukoya, Olubusola Adam, Manal Vu, Steve Kim, Minsu Tran, Diana Gómez, Nicolás Charpentier, Claire Sorour, Ingie Lacey, Tiara E. Tolstorukov, Michael Y. Sabatini, Bernardo L. Lee, Wei-Chung Allen Harwell, Corey C. Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development |
title | Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development |
title_full | Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development |
title_fullStr | Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development |
title_full_unstemmed | Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development |
title_short | Astrocyte-neuron crosstalk through Hedgehog signaling mediates cortical synapse development |
title_sort | astrocyte-neuron crosstalk through hedgehog signaling mediates cortical synapse development |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8962654/ https://www.ncbi.nlm.nih.gov/pubmed/35196485 http://dx.doi.org/10.1016/j.celrep.2022.110416 |
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