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Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?

Manganese (Mn) is an essential ubiquitous transition metal and, when occupationally or environmentally overexposed, a well-known risk factor for several neurological pathologies. However, the molecular mechanisms underlying Mn-induced neurotoxicity are largely unknown. In this study, addressing RNA-...

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Autores principales: Nicolai, Merle M., Pirritano, Marcello, Gasparoni, Gilles, Aschner, Michael, Simon, Martin, Bornhorst, Julia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502620/
https://www.ncbi.nlm.nih.gov/pubmed/36142660
http://dx.doi.org/10.3390/ijms231810748
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author Nicolai, Merle M.
Pirritano, Marcello
Gasparoni, Gilles
Aschner, Michael
Simon, Martin
Bornhorst, Julia
author_facet Nicolai, Merle M.
Pirritano, Marcello
Gasparoni, Gilles
Aschner, Michael
Simon, Martin
Bornhorst, Julia
author_sort Nicolai, Merle M.
collection PubMed
description Manganese (Mn) is an essential ubiquitous transition metal and, when occupationally or environmentally overexposed, a well-known risk factor for several neurological pathologies. However, the molecular mechanisms underlying Mn-induced neurotoxicity are largely unknown. In this study, addressing RNA-Seq analysis, bioavailability and survival assays, key pathways of transcriptional responses to Mn overexposure were investigated in the model organism Caenorhabditis elegans (C. elegans), providing insights into the Mn-induced cellular stress and damage response. Comparative transcriptome analyses identified a large number of differentially expressed genes (DEGs) in nematodes exposed to MnCl(2), and functional annotation suggested oxidative nucleotide damage, unfolded protein response and innate immunity as major damage response pathways. Additionally, a time-dependent increase in the transcriptional response after MnCl(2) exposure was identified by means of increased numbers of DEGs, indicating a time-dependent response and activation of the stress responses in Mn neurotoxicity. The data provided here represent a powerful transcriptomic resource in the field of Mn toxicity, and therefore, this study provides a useful basis for further planning of targeted mechanistic studies of Mn-induced neurotoxicity that are urgently needed in the face of increasing industrially caused environmental pollution with Mn.
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spelling pubmed-95026202022-09-24 Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome? Nicolai, Merle M. Pirritano, Marcello Gasparoni, Gilles Aschner, Michael Simon, Martin Bornhorst, Julia Int J Mol Sci Article Manganese (Mn) is an essential ubiquitous transition metal and, when occupationally or environmentally overexposed, a well-known risk factor for several neurological pathologies. However, the molecular mechanisms underlying Mn-induced neurotoxicity are largely unknown. In this study, addressing RNA-Seq analysis, bioavailability and survival assays, key pathways of transcriptional responses to Mn overexposure were investigated in the model organism Caenorhabditis elegans (C. elegans), providing insights into the Mn-induced cellular stress and damage response. Comparative transcriptome analyses identified a large number of differentially expressed genes (DEGs) in nematodes exposed to MnCl(2), and functional annotation suggested oxidative nucleotide damage, unfolded protein response and innate immunity as major damage response pathways. Additionally, a time-dependent increase in the transcriptional response after MnCl(2) exposure was identified by means of increased numbers of DEGs, indicating a time-dependent response and activation of the stress responses in Mn neurotoxicity. The data provided here represent a powerful transcriptomic resource in the field of Mn toxicity, and therefore, this study provides a useful basis for further planning of targeted mechanistic studies of Mn-induced neurotoxicity that are urgently needed in the face of increasing industrially caused environmental pollution with Mn. MDPI 2022-09-15 /pmc/articles/PMC9502620/ /pubmed/36142660 http://dx.doi.org/10.3390/ijms231810748 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Nicolai, Merle M.
Pirritano, Marcello
Gasparoni, Gilles
Aschner, Michael
Simon, Martin
Bornhorst, Julia
Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?
title Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?
title_full Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?
title_fullStr Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?
title_full_unstemmed Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?
title_short Manganese-Induced Toxicity in C. elegans: What Can We Learn from the Transcriptome?
title_sort manganese-induced toxicity in c. elegans: what can we learn from the transcriptome?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9502620/
https://www.ncbi.nlm.nih.gov/pubmed/36142660
http://dx.doi.org/10.3390/ijms231810748
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