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Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases
Bystin (BYSL) is a 306-amino acid protein encoded in humans by the BYSL gene located on the 6p21.1 chromosome. It is conserved across a wide range of eukaryotes. BYSL was reported to be a sensitive marker for the reactive astrocytes induced by ischemia/reperfusion and chemical hypoxia in vitro and i...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer US
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830468/ https://www.ncbi.nlm.nih.gov/pubmed/29349722 http://dx.doi.org/10.1007/s12024-017-9942-x |
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author | Olczak, Mieszko Chutorański, Dominik Kwiatkowska, Magdalena Samojłowicz, Dorota Tarka, Sylwia Wierzba-Bobrowicz, Teresa |
author_facet | Olczak, Mieszko Chutorański, Dominik Kwiatkowska, Magdalena Samojłowicz, Dorota Tarka, Sylwia Wierzba-Bobrowicz, Teresa |
author_sort | Olczak, Mieszko |
collection | PubMed |
description | Bystin (BYSL) is a 306-amino acid protein encoded in humans by the BYSL gene located on the 6p21.1 chromosome. It is conserved across a wide range of eukaryotes. BYSL was reported to be a sensitive marker for the reactive astrocytes induced by ischemia/reperfusion and chemical hypoxia in vitro and is considered to be one of the common characteristics of astrogliosis. In our study we examined whether BYSL could be used as a marker for hypoxic-ischemic changes in forensic cases. Groups suspected of acute hypoxic-ischemic changes presented strong BYSL expression in the cytoplasm of neocortical neurons especially in layers 3–5, that seemed to be short-lasting. In the hypoxic-ischemic-reperfusion group we did not find BYSL expression. BYSL expression in the cytoplasm of cortical neurons was minimal in the control group (cardiac arrest). BYSL seems to be a promising early marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases and certainly requires further studies. |
format | Online Article Text |
id | pubmed-5830468 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-58304682018-03-05 Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases Olczak, Mieszko Chutorański, Dominik Kwiatkowska, Magdalena Samojłowicz, Dorota Tarka, Sylwia Wierzba-Bobrowicz, Teresa Forensic Sci Med Pathol Original Article Bystin (BYSL) is a 306-amino acid protein encoded in humans by the BYSL gene located on the 6p21.1 chromosome. It is conserved across a wide range of eukaryotes. BYSL was reported to be a sensitive marker for the reactive astrocytes induced by ischemia/reperfusion and chemical hypoxia in vitro and is considered to be one of the common characteristics of astrogliosis. In our study we examined whether BYSL could be used as a marker for hypoxic-ischemic changes in forensic cases. Groups suspected of acute hypoxic-ischemic changes presented strong BYSL expression in the cytoplasm of neocortical neurons especially in layers 3–5, that seemed to be short-lasting. In the hypoxic-ischemic-reperfusion group we did not find BYSL expression. BYSL expression in the cytoplasm of cortical neurons was minimal in the control group (cardiac arrest). BYSL seems to be a promising early marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases and certainly requires further studies. Springer US 2018-01-18 2018 /pmc/articles/PMC5830468/ /pubmed/29349722 http://dx.doi.org/10.1007/s12024-017-9942-x Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Olczak, Mieszko Chutorański, Dominik Kwiatkowska, Magdalena Samojłowicz, Dorota Tarka, Sylwia Wierzba-Bobrowicz, Teresa Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
title | Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
title_full | Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
title_fullStr | Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
title_full_unstemmed | Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
title_short | Bystin (BYSL) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
title_sort | bystin (bysl) as a possible marker of severe hypoxic-ischemic changes in neuropathological examination of forensic cases |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5830468/ https://www.ncbi.nlm.nih.gov/pubmed/29349722 http://dx.doi.org/10.1007/s12024-017-9942-x |
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