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Developmental origin and local signals cooperate to determine septal astrocyte identity

Astrocyte specification during development is influenced by both intrinsic and extrinsic factors, but the precise contribution of each remains poorly understood. Here we show that septal astrocytes from Nkx2.1 and Zic4 expressing progenitor zones are allocated into non-overlapping domains of the med...

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Autores principales: Xie, Yajun, Reid, Christopher M., Granados, Alejandro A., Garcia, Miguel Turrero, Dale-Huang, Fiona, Hanson, Sarah M., Mancia, Walter, Liu, Jonathan, Adam, Manal, Mosto, Olivia, Pisco, Angela O., Alvarez-Buylla, Arturo, Harwell, Corey C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592657/
https://www.ncbi.nlm.nih.gov/pubmed/37873089
http://dx.doi.org/10.1101/2023.10.08.561428
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author Xie, Yajun
Reid, Christopher M.
Granados, Alejandro A.
Garcia, Miguel Turrero
Dale-Huang, Fiona
Hanson, Sarah M.
Mancia, Walter
Liu, Jonathan
Adam, Manal
Mosto, Olivia
Pisco, Angela O.
Alvarez-Buylla, Arturo
Harwell, Corey C.
author_facet Xie, Yajun
Reid, Christopher M.
Granados, Alejandro A.
Garcia, Miguel Turrero
Dale-Huang, Fiona
Hanson, Sarah M.
Mancia, Walter
Liu, Jonathan
Adam, Manal
Mosto, Olivia
Pisco, Angela O.
Alvarez-Buylla, Arturo
Harwell, Corey C.
author_sort Xie, Yajun
collection PubMed
description Astrocyte specification during development is influenced by both intrinsic and extrinsic factors, but the precise contribution of each remains poorly understood. Here we show that septal astrocytes from Nkx2.1 and Zic4 expressing progenitor zones are allocated into non-overlapping domains of the medial (MS) and lateral septal nuclei (LS) respectively. Astrocytes in these areas exhibit distinctive molecular and morphological features tailored to the unique cellular and synaptic circuit environment of each nucleus. Using single-nucleus (sn) RNA sequencing, we trace the developmental trajectories of cells in the septum and find that neurons and astrocytes undergo region and developmental stage-specific local cell-cell interactions. We show that expression of the classic morphogens Sonic hedgehog (Shh) and Fibroblast growth factors (Fgfs) by MS and LS neurons respectively, functions to promote the molecular specification of local astrocytes in each region. Finally, using heterotopic cell transplantation, we show that both morphological and molecular specifications of septal astrocytes are highly dependent on the local microenvironment, regardless of developmental origins. Our data highlights the complex interplay between intrinsic and extrinsic factors shaping astrocyte identities and illustrates the importance of the local environment in determining astrocyte functional specialization.
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spelling pubmed-105926572023-10-24 Developmental origin and local signals cooperate to determine septal astrocyte identity Xie, Yajun Reid, Christopher M. Granados, Alejandro A. Garcia, Miguel Turrero Dale-Huang, Fiona Hanson, Sarah M. Mancia, Walter Liu, Jonathan Adam, Manal Mosto, Olivia Pisco, Angela O. Alvarez-Buylla, Arturo Harwell, Corey C. bioRxiv Article Astrocyte specification during development is influenced by both intrinsic and extrinsic factors, but the precise contribution of each remains poorly understood. Here we show that septal astrocytes from Nkx2.1 and Zic4 expressing progenitor zones are allocated into non-overlapping domains of the medial (MS) and lateral septal nuclei (LS) respectively. Astrocytes in these areas exhibit distinctive molecular and morphological features tailored to the unique cellular and synaptic circuit environment of each nucleus. Using single-nucleus (sn) RNA sequencing, we trace the developmental trajectories of cells in the septum and find that neurons and astrocytes undergo region and developmental stage-specific local cell-cell interactions. We show that expression of the classic morphogens Sonic hedgehog (Shh) and Fibroblast growth factors (Fgfs) by MS and LS neurons respectively, functions to promote the molecular specification of local astrocytes in each region. Finally, using heterotopic cell transplantation, we show that both morphological and molecular specifications of septal astrocytes are highly dependent on the local microenvironment, regardless of developmental origins. Our data highlights the complex interplay between intrinsic and extrinsic factors shaping astrocyte identities and illustrates the importance of the local environment in determining astrocyte functional specialization. Cold Spring Harbor Laboratory 2023-10-10 /pmc/articles/PMC10592657/ /pubmed/37873089 http://dx.doi.org/10.1101/2023.10.08.561428 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Xie, Yajun
Reid, Christopher M.
Granados, Alejandro A.
Garcia, Miguel Turrero
Dale-Huang, Fiona
Hanson, Sarah M.
Mancia, Walter
Liu, Jonathan
Adam, Manal
Mosto, Olivia
Pisco, Angela O.
Alvarez-Buylla, Arturo
Harwell, Corey C.
Developmental origin and local signals cooperate to determine septal astrocyte identity
title Developmental origin and local signals cooperate to determine septal astrocyte identity
title_full Developmental origin and local signals cooperate to determine septal astrocyte identity
title_fullStr Developmental origin and local signals cooperate to determine septal astrocyte identity
title_full_unstemmed Developmental origin and local signals cooperate to determine septal astrocyte identity
title_short Developmental origin and local signals cooperate to determine septal astrocyte identity
title_sort developmental origin and local signals cooperate to determine septal astrocyte identity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10592657/
https://www.ncbi.nlm.nih.gov/pubmed/37873089
http://dx.doi.org/10.1101/2023.10.08.561428
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