Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?

Extracellular pH is an important parameter influencing cell function and fate. Microenvironmental acidosis accompanies different pathological situations, including inflammation, hypoxia and ischemia. Research focussed mainly on acidification of the tumour micromilieu and the possible consequences on...

Full description

Saved in:
Bibliographic Details
Main Authors: Virginie Dubourg, Marie-Christin Schulz, Philipp Terpe, Stefanie Ruhs, Michael Kopf, Michael Gekle
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2023-01-01
Series:PLoS ONE
Online Access:https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0290373&type=printable
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849687233914732544
author Virginie Dubourg
Marie-Christin Schulz
Philipp Terpe
Stefanie Ruhs
Michael Kopf
Michael Gekle
author_facet Virginie Dubourg
Marie-Christin Schulz
Philipp Terpe
Stefanie Ruhs
Michael Kopf
Michael Gekle
author_sort Virginie Dubourg
collection DOAJ
description Extracellular pH is an important parameter influencing cell function and fate. Microenvironmental acidosis accompanies different pathological situations, including inflammation, hypoxia and ischemia. Research focussed mainly on acidification of the tumour micromilieu and the possible consequences on proliferation, migration and drug resistance. Much less is known regarding the impact of microenvironmental acidosis on the transcriptome of non-tumour cells, which are exposed to local acidosis during inflammation, hypoxia, ischemia or metabolic derailment. In the present hypothesis-generating study, we investigated the transcriptional impact of extracellular acidosis on five non-tumour cell types of human and rat origin, combining RNA-Sequencing and extensive bioinformatics analyses. For this purpose, cell type-dependent acidosis resiliences and acidosis-induced transcriptional changes within these resilience ranges were determined, using 56 biological samples. The RNA-Sequencing results were used for dual differential-expression analysis (DESeq and edgeR) and, after appropriate homology mapping, Gene Ontology enrichment analysis (g:Profiler), Ingenuity Pathway Analysis (IPA®), as well as functional enrichment analysis for predicted upstream regulators, were performed. Extracellular acidosis led to substantial, yet different, quantitative transcriptional alterations in all five cell types. Our results identify the regulator of the transcriptional activity NCOA5 as the only general acidosis-responsive gene. Although we observed a species- and cell type-dominated response regarding gene expression regulation, Gene Ontology enrichment analysis and upstream regulator analysis predicted a general acidosis response pattern. Indeed, they suggested the regulation of four general acidosis-responsive cellular networks, which comprised the integrated stress response (ISR), TGF-β signalling, NFE2L2 and TP53. Future studies will have to extend the results of our bioinformatics analyses to cell biological and cell physiological validation experiments, in order to test the refined working hypothesis here.
format Article
id doaj-art-360195c8a1d14d38b2775731fb86792c
institution DOAJ
issn 1932-6203
language English
publishDate 2023-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj-art-360195c8a1d14d38b2775731fb86792c2025-08-20T03:22:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032023-01-01188e029037310.1371/journal.pone.0290373Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?Virginie DubourgMarie-Christin SchulzPhilipp TerpeStefanie RuhsMichael KopfMichael GekleExtracellular pH is an important parameter influencing cell function and fate. Microenvironmental acidosis accompanies different pathological situations, including inflammation, hypoxia and ischemia. Research focussed mainly on acidification of the tumour micromilieu and the possible consequences on proliferation, migration and drug resistance. Much less is known regarding the impact of microenvironmental acidosis on the transcriptome of non-tumour cells, which are exposed to local acidosis during inflammation, hypoxia, ischemia or metabolic derailment. In the present hypothesis-generating study, we investigated the transcriptional impact of extracellular acidosis on five non-tumour cell types of human and rat origin, combining RNA-Sequencing and extensive bioinformatics analyses. For this purpose, cell type-dependent acidosis resiliences and acidosis-induced transcriptional changes within these resilience ranges were determined, using 56 biological samples. The RNA-Sequencing results were used for dual differential-expression analysis (DESeq and edgeR) and, after appropriate homology mapping, Gene Ontology enrichment analysis (g:Profiler), Ingenuity Pathway Analysis (IPA®), as well as functional enrichment analysis for predicted upstream regulators, were performed. Extracellular acidosis led to substantial, yet different, quantitative transcriptional alterations in all five cell types. Our results identify the regulator of the transcriptional activity NCOA5 as the only general acidosis-responsive gene. Although we observed a species- and cell type-dominated response regarding gene expression regulation, Gene Ontology enrichment analysis and upstream regulator analysis predicted a general acidosis response pattern. Indeed, they suggested the regulation of four general acidosis-responsive cellular networks, which comprised the integrated stress response (ISR), TGF-β signalling, NFE2L2 and TP53. Future studies will have to extend the results of our bioinformatics analyses to cell biological and cell physiological validation experiments, in order to test the refined working hypothesis here.https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0290373&type=printable
spellingShingle Virginie Dubourg
Marie-Christin Schulz
Philipp Terpe
Stefanie Ruhs
Michael Kopf
Michael Gekle
Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?
PLoS ONE
title Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?
title_full Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?
title_fullStr Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?
title_full_unstemmed Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?
title_short Hypothesis-generating analysis of the impact of non-damaging metabolic acidosis on the transcriptome of different cell types: Integrated stress response (ISR) modulation as general transcriptomic reaction to non-respiratory acidic stress?
title_sort hypothesis generating analysis of the impact of non damaging metabolic acidosis on the transcriptome of different cell types integrated stress response isr modulation as general transcriptomic reaction to non respiratory acidic stress
url https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0290373&type=printable
work_keys_str_mv AT virginiedubourg hypothesisgeneratinganalysisoftheimpactofnondamagingmetabolicacidosisonthetranscriptomeofdifferentcelltypesintegratedstressresponseisrmodulationasgeneraltranscriptomicreactiontononrespiratoryacidicstress
AT mariechristinschulz hypothesisgeneratinganalysisoftheimpactofnondamagingmetabolicacidosisonthetranscriptomeofdifferentcelltypesintegratedstressresponseisrmodulationasgeneraltranscriptomicreactiontononrespiratoryacidicstress
AT philippterpe hypothesisgeneratinganalysisoftheimpactofnondamagingmetabolicacidosisonthetranscriptomeofdifferentcelltypesintegratedstressresponseisrmodulationasgeneraltranscriptomicreactiontononrespiratoryacidicstress
AT stefanieruhs hypothesisgeneratinganalysisoftheimpactofnondamagingmetabolicacidosisonthetranscriptomeofdifferentcelltypesintegratedstressresponseisrmodulationasgeneraltranscriptomicreactiontononrespiratoryacidicstress
AT michaelkopf hypothesisgeneratinganalysisoftheimpactofnondamagingmetabolicacidosisonthetranscriptomeofdifferentcelltypesintegratedstressresponseisrmodulationasgeneraltranscriptomicreactiontononrespiratoryacidicstress
AT michaelgekle hypothesisgeneratinganalysisoftheimpactofnondamagingmetabolicacidosisonthetranscriptomeofdifferentcelltypesintegratedstressresponseisrmodulationasgeneraltranscriptomicreactiontononrespiratoryacidicstress