Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile

Oxygen is an essential factor in the cellular microenvironment with pivotal effects on neural development with a particular sensitivity of midbrain neural stem cells (NSCs) to high atmospheric oxygen tension. However, most experiments are still performed at atmospheric O2 levels (21%, normoxia), whe...

Full description

Bibliographic Details
Main Authors: Lena Braunschweig, Jennifer Lanto, Anne K. Meyer, Franz Markert, Alexander Storch
Format: Article
Language:English
Published: Hindawi Limited 2022-01-01
Series:Stem Cells International
Online Access:http://dx.doi.org/10.1155/2022/6718640
_version_ 1811189365851815936
author Lena Braunschweig
Jennifer Lanto
Anne K. Meyer
Franz Markert
Alexander Storch
author_facet Lena Braunschweig
Jennifer Lanto
Anne K. Meyer
Franz Markert
Alexander Storch
author_sort Lena Braunschweig
collection DOAJ
description Oxygen is an essential factor in the cellular microenvironment with pivotal effects on neural development with a particular sensitivity of midbrain neural stem cells (NSCs) to high atmospheric oxygen tension. However, most experiments are still performed at atmospheric O2 levels (21%, normoxia), whereas mammalian brain tissue is physiologically exposed to substantially lower O2 tensions around 3% (physioxia). We here performed serial Affymetrix gene array analyses to detect expression changes in mouse fetal NSCs from both midbrain and cortical tissues when kept at physioxia compared to normoxia. We identified more than 400 O2-regulated genes involved in cellular metabolism, cell proliferation/differentiation, and various signaling pathways. NSCs from both regions showed a low number but high conformity of regulated genes (9 genes in midbrain vs. 34 in cortical NSCs; 8 concordant expression changes) after short-term physioxia (2 days) with metabolic processes and cellular processes being the most prominent GO categories pointing to cellular adaption to lower oxygen levels. Gene expression profiles changed dramatically after long-term physioxia (13 days) with a higher number of regulated genes and more diverse expression patterns when comparing the two NSC types (338 genes in midbrain vs. 121 in cortical NSCs; 75 concordant changes). Most prominently, we observed a reduction of hits in metabolic processes but an increase in biological regulation and signaling pointing to a switch towards signaling processes and stem cell maintenance. Our data may serve as a basis for identifying potential signaling pathways that maintain stem cell characteristics in cortical versus midbrain physioxic stem cell niches.
first_indexed 2024-04-11T14:33:47Z
format Article
id doaj.art-13a478f2d30148e2bc1f77cdc38d6267
institution Directory Open Access Journal
issn 1687-9678
language English
last_indexed 2024-04-11T14:33:47Z
publishDate 2022-01-01
publisher Hindawi Limited
record_format Article
series Stem Cells International
spelling doaj.art-13a478f2d30148e2bc1f77cdc38d62672022-12-22T04:18:24ZengHindawi LimitedStem Cells International1687-96782022-01-01202210.1155/2022/6718640Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling ProfileLena Braunschweig0Jennifer Lanto1Anne K. Meyer2Franz Markert3Alexander Storch4Division of Neurodegenerative DiseasesDepartment of NeurologyDivision of Neurodegenerative DiseasesDepartment of NeurologyDivision of Neurodegenerative DiseasesOxygen is an essential factor in the cellular microenvironment with pivotal effects on neural development with a particular sensitivity of midbrain neural stem cells (NSCs) to high atmospheric oxygen tension. However, most experiments are still performed at atmospheric O2 levels (21%, normoxia), whereas mammalian brain tissue is physiologically exposed to substantially lower O2 tensions around 3% (physioxia). We here performed serial Affymetrix gene array analyses to detect expression changes in mouse fetal NSCs from both midbrain and cortical tissues when kept at physioxia compared to normoxia. We identified more than 400 O2-regulated genes involved in cellular metabolism, cell proliferation/differentiation, and various signaling pathways. NSCs from both regions showed a low number but high conformity of regulated genes (9 genes in midbrain vs. 34 in cortical NSCs; 8 concordant expression changes) after short-term physioxia (2 days) with metabolic processes and cellular processes being the most prominent GO categories pointing to cellular adaption to lower oxygen levels. Gene expression profiles changed dramatically after long-term physioxia (13 days) with a higher number of regulated genes and more diverse expression patterns when comparing the two NSC types (338 genes in midbrain vs. 121 in cortical NSCs; 75 concordant changes). Most prominently, we observed a reduction of hits in metabolic processes but an increase in biological regulation and signaling pointing to a switch towards signaling processes and stem cell maintenance. Our data may serve as a basis for identifying potential signaling pathways that maintain stem cell characteristics in cortical versus midbrain physioxic stem cell niches.http://dx.doi.org/10.1155/2022/6718640
spellingShingle Lena Braunschweig
Jennifer Lanto
Anne K. Meyer
Franz Markert
Alexander Storch
Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile
Stem Cells International
title Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile
title_full Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile
title_fullStr Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile
title_full_unstemmed Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile
title_short Serial Gene Expression Profiling of Neural Stem Cells Shows Transcriptome Switch by Long-Term Physioxia from Metabolic Adaption to Cell Signaling Profile
title_sort serial gene expression profiling of neural stem cells shows transcriptome switch by long term physioxia from metabolic adaption to cell signaling profile
url http://dx.doi.org/10.1155/2022/6718640
work_keys_str_mv AT lenabraunschweig serialgeneexpressionprofilingofneuralstemcellsshowstranscriptomeswitchbylongtermphysioxiafrommetabolicadaptiontocellsignalingprofile
AT jenniferlanto serialgeneexpressionprofilingofneuralstemcellsshowstranscriptomeswitchbylongtermphysioxiafrommetabolicadaptiontocellsignalingprofile
AT annekmeyer serialgeneexpressionprofilingofneuralstemcellsshowstranscriptomeswitchbylongtermphysioxiafrommetabolicadaptiontocellsignalingprofile
AT franzmarkert serialgeneexpressionprofilingofneuralstemcellsshowstranscriptomeswitchbylongtermphysioxiafrommetabolicadaptiontocellsignalingprofile
AT alexanderstorch serialgeneexpressionprofilingofneuralstemcellsshowstranscriptomeswitchbylongtermphysioxiafrommetabolicadaptiontocellsignalingprofile