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Extracellular circulating miRNAs as stress-related signature to search and rescue dogs
Our research explores serum extracellular circulating miRNAs (ecmiRNAs) involved in dog stress response immediately after the search and rescue (SAR) of missing people. The experimental plan considers four arduous SAR simulations. The SAR dogs are trained by the Alpine School of the Military Force o...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881509/ https://www.ncbi.nlm.nih.gov/pubmed/35217704 http://dx.doi.org/10.1038/s41598-022-07131-5 |
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author | Guelfi, Gabriella Iaboni, Martina Sansone, Anna Capaccia, Camilla Santoro, Michele Matteo Diverio, Silvana |
author_facet | Guelfi, Gabriella Iaboni, Martina Sansone, Anna Capaccia, Camilla Santoro, Michele Matteo Diverio, Silvana |
author_sort | Guelfi, Gabriella |
collection | PubMed |
description | Our research explores serum extracellular circulating miRNAs (ecmiRNAs) involved in dog stress response immediately after the search and rescue (SAR) of missing people. The experimental plan considers four arduous SAR simulations. The SAR dogs are trained by the Alpine School of the Military Force of Guardia di Finanza (Passo Rolle, Italy). The First SAR Trial analyzed dog serum samples at rest time (T0), and immediately after SAR performance (T1) using the miRNome-wide screening next-generation sequencing (NGS). T1 versus T0 NGS results revealed a different expression level of let-7a and let-7f. Subsequently, in a large sample size including: 1st (n = 6), 2nd (n = 6), 3rd (n = 6), and 4th (n = 4) trials, let-7a and let-7f were validated by qPCR. Bioinformatics analysis with TarBase (v.8) and the Diana-mirPath (v.3) revealed a functional role of let-7a and let-7f in the p53 pathway to restore cellular homeostasis. Let-7a and let-7f, highly expressed at T1, could stop MDMs-p53 inhibition inducing the p53 increase in level. In addition, let-7a and let-7f, via p53 post-transcriptional regulation, buffers p53 transcription spikes. During SAR stress, the possibility of p53 preconditioning could explain the phenomenon of “stress hardening” where the tolerance of particular stress increases after preconditioning. |
format | Online Article Text |
id | pubmed-8881509 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-88815092022-03-01 Extracellular circulating miRNAs as stress-related signature to search and rescue dogs Guelfi, Gabriella Iaboni, Martina Sansone, Anna Capaccia, Camilla Santoro, Michele Matteo Diverio, Silvana Sci Rep Article Our research explores serum extracellular circulating miRNAs (ecmiRNAs) involved in dog stress response immediately after the search and rescue (SAR) of missing people. The experimental plan considers four arduous SAR simulations. The SAR dogs are trained by the Alpine School of the Military Force of Guardia di Finanza (Passo Rolle, Italy). The First SAR Trial analyzed dog serum samples at rest time (T0), and immediately after SAR performance (T1) using the miRNome-wide screening next-generation sequencing (NGS). T1 versus T0 NGS results revealed a different expression level of let-7a and let-7f. Subsequently, in a large sample size including: 1st (n = 6), 2nd (n = 6), 3rd (n = 6), and 4th (n = 4) trials, let-7a and let-7f were validated by qPCR. Bioinformatics analysis with TarBase (v.8) and the Diana-mirPath (v.3) revealed a functional role of let-7a and let-7f in the p53 pathway to restore cellular homeostasis. Let-7a and let-7f, highly expressed at T1, could stop MDMs-p53 inhibition inducing the p53 increase in level. In addition, let-7a and let-7f, via p53 post-transcriptional regulation, buffers p53 transcription spikes. During SAR stress, the possibility of p53 preconditioning could explain the phenomenon of “stress hardening” where the tolerance of particular stress increases after preconditioning. Nature Publishing Group UK 2022-02-25 /pmc/articles/PMC8881509/ /pubmed/35217704 http://dx.doi.org/10.1038/s41598-022-07131-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Guelfi, Gabriella Iaboni, Martina Sansone, Anna Capaccia, Camilla Santoro, Michele Matteo Diverio, Silvana Extracellular circulating miRNAs as stress-related signature to search and rescue dogs |
title | Extracellular circulating miRNAs as stress-related signature to search and rescue dogs |
title_full | Extracellular circulating miRNAs as stress-related signature to search and rescue dogs |
title_fullStr | Extracellular circulating miRNAs as stress-related signature to search and rescue dogs |
title_full_unstemmed | Extracellular circulating miRNAs as stress-related signature to search and rescue dogs |
title_short | Extracellular circulating miRNAs as stress-related signature to search and rescue dogs |
title_sort | extracellular circulating mirnas as stress-related signature to search and rescue dogs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8881509/ https://www.ncbi.nlm.nih.gov/pubmed/35217704 http://dx.doi.org/10.1038/s41598-022-07131-5 |
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