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HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue
Estimating the post mortem interval (PMI) is still a crucial step in Forensic Pathology. Although several methods are available for assessing the PMI, a precise estimation is still quite unreliable and can be inaccurate. The present study aimed to investigate the immunohistochemical distribution and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980163/ https://www.ncbi.nlm.nih.gov/pubmed/29504141 http://dx.doi.org/10.1111/joa.12800 |
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author | Fais, Paolo Mazzotti, Maria Carla Teti, Gabriella Boscolo‐Berto, Rafael Pelotti, Susi Falconi, Mirella |
author_facet | Fais, Paolo Mazzotti, Maria Carla Teti, Gabriella Boscolo‐Berto, Rafael Pelotti, Susi Falconi, Mirella |
author_sort | Fais, Paolo |
collection | PubMed |
description | Estimating the post mortem interval (PMI) is still a crucial step in Forensic Pathology. Although several methods are available for assessing the PMI, a precise estimation is still quite unreliable and can be inaccurate. The present study aimed to investigate the immunohistochemical distribution and mRNA expression of hypoxia inducible factor (HIF‐1α) in post mortem gingival tissues to establish a correlation between the presence of HIF‐1α and the time since death, with the final goal of achieving a more accurate PMI estimation. Samples of gingival tissues were obtained from 10 cadavers at different PMIs (1–3 days, 4–5 days and 8–9 days), and were processed for immunohistochemistry and quantitative reverse transcription‐polymerase chain reaction. The results showed a time‐dependent correlation of HIF‐1α protein and its mRNA with different times since death, which suggests that HIF‐1α is a potential marker for PMI estimation. The results showed a high HIF‐1α protein signal that was mainly localized in the stratum basale of the oral mucosa in samples collected at a short PMI (1–3 days). It gradually decreased in samples collected at a medium PMI (4–5 days), but it was not detected in samples collected at a long PMI (8–9 days). These results are in agreement with the mRNA data. These data indicate an interesting potential utility of Forensic Anatomy‐based techniques, such as immunohistochemistry, as important complementary tools to be used in forensic investigations. |
format | Online Article Text |
id | pubmed-5980163 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59801632018-06-06 HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue Fais, Paolo Mazzotti, Maria Carla Teti, Gabriella Boscolo‐Berto, Rafael Pelotti, Susi Falconi, Mirella J Anat Brief Communication Estimating the post mortem interval (PMI) is still a crucial step in Forensic Pathology. Although several methods are available for assessing the PMI, a precise estimation is still quite unreliable and can be inaccurate. The present study aimed to investigate the immunohistochemical distribution and mRNA expression of hypoxia inducible factor (HIF‐1α) in post mortem gingival tissues to establish a correlation between the presence of HIF‐1α and the time since death, with the final goal of achieving a more accurate PMI estimation. Samples of gingival tissues were obtained from 10 cadavers at different PMIs (1–3 days, 4–5 days and 8–9 days), and were processed for immunohistochemistry and quantitative reverse transcription‐polymerase chain reaction. The results showed a time‐dependent correlation of HIF‐1α protein and its mRNA with different times since death, which suggests that HIF‐1α is a potential marker for PMI estimation. The results showed a high HIF‐1α protein signal that was mainly localized in the stratum basale of the oral mucosa in samples collected at a short PMI (1–3 days). It gradually decreased in samples collected at a medium PMI (4–5 days), but it was not detected in samples collected at a long PMI (8–9 days). These results are in agreement with the mRNA data. These data indicate an interesting potential utility of Forensic Anatomy‐based techniques, such as immunohistochemistry, as important complementary tools to be used in forensic investigations. John Wiley and Sons Inc. 2018-03-05 2018-06 /pmc/articles/PMC5980163/ /pubmed/29504141 http://dx.doi.org/10.1111/joa.12800 Text en © 2018 The Authors. Journal of Anatomy published by John Wiley & Sons Ltd on behalf of Anatomical Society. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Brief Communication Fais, Paolo Mazzotti, Maria Carla Teti, Gabriella Boscolo‐Berto, Rafael Pelotti, Susi Falconi, Mirella HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue |
title |
HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue |
title_full |
HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue |
title_fullStr |
HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue |
title_full_unstemmed |
HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue |
title_short |
HIF1α protein and mRNA expression as a new marker for post mortem interval estimation in human gingival tissue |
title_sort | hif1α protein and mrna expression as a new marker for post mortem interval estimation in human gingival tissue |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5980163/ https://www.ncbi.nlm.nih.gov/pubmed/29504141 http://dx.doi.org/10.1111/joa.12800 |
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