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Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA

Oriens lacunosum-moleculare (O-LM) interneurons constitute 40% of hippocampal interneurons expressing Somatostatin (SST). Recent evidence has indicated a dual origin for these cells in the medial and caudal ganglionic eminences (MGE and CGE), with expression of Htr3a as a distinguishing factor. This...

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Autores principales: Asgarian, Zeinab, Magno, Lorenza, Ktena, Niki, Harris, Kenneth D., Kessaris, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895756/
https://www.ncbi.nlm.nih.gov/pubmed/31631021
http://dx.doi.org/10.1016/j.stemcr.2019.09.008
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author Asgarian, Zeinab
Magno, Lorenza
Ktena, Niki
Harris, Kenneth D.
Kessaris, Nicoletta
author_facet Asgarian, Zeinab
Magno, Lorenza
Ktena, Niki
Harris, Kenneth D.
Kessaris, Nicoletta
author_sort Asgarian, Zeinab
collection PubMed
description Oriens lacunosum-moleculare (O-LM) interneurons constitute 40% of hippocampal interneurons expressing Somatostatin (SST). Recent evidence has indicated a dual origin for these cells in the medial and caudal ganglionic eminences (MGE and CGE), with expression of Htr3a as a distinguishing factor. This is strikingly different from cortical SST interneurons that have a single origin within the MGE/preoptic area (POA). We reassessed the origin of hippocampal SST interneurons using a range of genetic lineage-tracing mice combined with single-cell transcriptomic analysis. We find a common origin for all hippocampal SST interneurons in NKX2-1-expressing progenitors of the telencephalic neuroepithelium and an MGE/POA-like transcriptomic signature for all SST clusters. This suggests that functional heterogeneity within the SST CA1 population cannot be attributed to a differential MGE/CGE genetic origin.
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spelling pubmed-68957562019-12-16 Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA Asgarian, Zeinab Magno, Lorenza Ktena, Niki Harris, Kenneth D. Kessaris, Nicoletta Stem Cell Reports Report Oriens lacunosum-moleculare (O-LM) interneurons constitute 40% of hippocampal interneurons expressing Somatostatin (SST). Recent evidence has indicated a dual origin for these cells in the medial and caudal ganglionic eminences (MGE and CGE), with expression of Htr3a as a distinguishing factor. This is strikingly different from cortical SST interneurons that have a single origin within the MGE/preoptic area (POA). We reassessed the origin of hippocampal SST interneurons using a range of genetic lineage-tracing mice combined with single-cell transcriptomic analysis. We find a common origin for all hippocampal SST interneurons in NKX2-1-expressing progenitors of the telencephalic neuroepithelium and an MGE/POA-like transcriptomic signature for all SST clusters. This suggests that functional heterogeneity within the SST CA1 population cannot be attributed to a differential MGE/CGE genetic origin. Elsevier 2019-10-17 /pmc/articles/PMC6895756/ /pubmed/31631021 http://dx.doi.org/10.1016/j.stemcr.2019.09.008 Text en © 2019 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Report
Asgarian, Zeinab
Magno, Lorenza
Ktena, Niki
Harris, Kenneth D.
Kessaris, Nicoletta
Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA
title Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA
title_full Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA
title_fullStr Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA
title_full_unstemmed Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA
title_short Hippocampal CA1 Somatostatin Interneurons Originate in the Embryonic MGE/POA
title_sort hippocampal ca1 somatostatin interneurons originate in the embryonic mge/poa
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6895756/
https://www.ncbi.nlm.nih.gov/pubmed/31631021
http://dx.doi.org/10.1016/j.stemcr.2019.09.008
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