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Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications

The aim of this pilot study was to investigate the diagnostic potential of TMEM119 as a useful microglia-specific marker in combination with immunostainings for phagocytic function and infiltrating capacity of monocytes in cases of lethal monosubstance intoxications by morphine (MOR), methamphetamin...

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Autores principales: Bohnert, Simone, Georgiades, Kosmas, Monoranu, Camelia-Maria, Bohnert, Michael, Büttner, Andreas, Ondruschka, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523458/
https://www.ncbi.nlm.nih.gov/pubmed/34553260
http://dx.doi.org/10.1007/s00414-021-02699-5
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author Bohnert, Simone
Georgiades, Kosmas
Monoranu, Camelia-Maria
Bohnert, Michael
Büttner, Andreas
Ondruschka, Benjamin
author_facet Bohnert, Simone
Georgiades, Kosmas
Monoranu, Camelia-Maria
Bohnert, Michael
Büttner, Andreas
Ondruschka, Benjamin
author_sort Bohnert, Simone
collection PubMed
description The aim of this pilot study was to investigate the diagnostic potential of TMEM119 as a useful microglia-specific marker in combination with immunostainings for phagocytic function and infiltrating capacity of monocytes in cases of lethal monosubstance intoxications by morphine (MOR), methamphetamine (METH), and of ethanol-associated death (ETH) respectively. Human brain tissue samples were obtained from forensic autopsies of cases with single substance abuse (MOR, n = 8; ETH, n = 10; METH, n = 9) and then compared to a cohort of cardiovascular fatalities as controls (n = 9). Brain tissue samples of cortex, white matter, and hippocampus were collected and stained immunohistochemically with antibodies against TMEM119, CD68KiM1P, and CCR2. We could document the lowest density of TMEM119-positive cells in MOR deaths with highly significant differences to the control densities in all three regions investigated. In ETH and METH deaths, the expression of TMEM119 was comparable to cell densities in controls. The results indicate that the immunoreaction in brain tissue is different in these groups depending on the drug type used for abuse. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00414-021-02699-5.
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spelling pubmed-85234582021-10-22 Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications Bohnert, Simone Georgiades, Kosmas Monoranu, Camelia-Maria Bohnert, Michael Büttner, Andreas Ondruschka, Benjamin Int J Legal Med Short Communication The aim of this pilot study was to investigate the diagnostic potential of TMEM119 as a useful microglia-specific marker in combination with immunostainings for phagocytic function and infiltrating capacity of monocytes in cases of lethal monosubstance intoxications by morphine (MOR), methamphetamine (METH), and of ethanol-associated death (ETH) respectively. Human brain tissue samples were obtained from forensic autopsies of cases with single substance abuse (MOR, n = 8; ETH, n = 10; METH, n = 9) and then compared to a cohort of cardiovascular fatalities as controls (n = 9). Brain tissue samples of cortex, white matter, and hippocampus were collected and stained immunohistochemically with antibodies against TMEM119, CD68KiM1P, and CCR2. We could document the lowest density of TMEM119-positive cells in MOR deaths with highly significant differences to the control densities in all three regions investigated. In ETH and METH deaths, the expression of TMEM119 was comparable to cell densities in controls. The results indicate that the immunoreaction in brain tissue is different in these groups depending on the drug type used for abuse. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00414-021-02699-5. Springer Berlin Heidelberg 2021-09-22 2021 /pmc/articles/PMC8523458/ /pubmed/34553260 http://dx.doi.org/10.1007/s00414-021-02699-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 Short Communication
Bohnert, Simone
Georgiades, Kosmas
Monoranu, Camelia-Maria
Bohnert, Michael
Büttner, Andreas
Ondruschka, Benjamin
Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications
title Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications
title_full Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications
title_fullStr Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications
title_full_unstemmed Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications
title_short Quantitative evidence of suppressed TMEM119 microglial immunohistochemistry in fatal morphine intoxications
title_sort quantitative evidence of suppressed tmem119 microglial immunohistochemistry in fatal morphine intoxications
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8523458/
https://www.ncbi.nlm.nih.gov/pubmed/34553260
http://dx.doi.org/10.1007/s00414-021-02699-5
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