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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-...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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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. |
format | Online Article Text |
id | pubmed-9502620 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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