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Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury

BACKGROUND: Enhanced glycolysis leads to elevated levels of the toxic metabolite methylglyoxal which contributes to loss of protein-function, metabolic imbalance and cell death. Neurons were shown being highly susceptible to methylglyoxal toxicity. Glyoxalase 1 as an ubiquitous enzyme reflects the m...

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Autores principales: Pieroh, Philipp, Koch, Marco, Wagner, Daniel-Christoph, Boltze, Johannes, Ehrlich, Angela, Ghadban, Chalid, Hobusch, Constance, Birkenmeier, Gerd, Dehghani, Faramarz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911945/
https://www.ncbi.nlm.nih.gov/pubmed/24498315
http://dx.doi.org/10.1371/journal.pone.0087364
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author Pieroh, Philipp
Koch, Marco
Wagner, Daniel-Christoph
Boltze, Johannes
Ehrlich, Angela
Ghadban, Chalid
Hobusch, Constance
Birkenmeier, Gerd
Dehghani, Faramarz
author_facet Pieroh, Philipp
Koch, Marco
Wagner, Daniel-Christoph
Boltze, Johannes
Ehrlich, Angela
Ghadban, Chalid
Hobusch, Constance
Birkenmeier, Gerd
Dehghani, Faramarz
author_sort Pieroh, Philipp
collection PubMed
description BACKGROUND: Enhanced glycolysis leads to elevated levels of the toxic metabolite methylglyoxal which contributes to loss of protein-function, metabolic imbalance and cell death. Neurons were shown being highly susceptible to methylglyoxal toxicity. Glyoxalase 1 as an ubiquitous enzyme reflects the main detoxifying enzyme of methylglyoxal and underlies changes during aging and neurodegeneration. However, little is known about dynamics of Glyoxalase 1 following neuronal lesions so far. METHODS: To determine a possible involvement of Glyoxalase 1 in acute brain injury, we analysed the temporal dynamics of Glyoxalase 1 distribution and expression by immunohistochemistry and Western Blot analysis. Organotypic hippocampal slice cultures were excitotoxically (N-methyl-D-aspartate, 50 µM for 4 hours) lesioned in vitro (5 minutes to 72 hours). Additionally, permanent middle cerebral artery occlusion was performed (75 minutes to 60 days). RESULTS: We found (i) a predominant localisation of Glyoxalase 1 in endothelial cells in non-lesioned brains (ii) a time-dependent up-regulation and re-distribution of Glyoxalase 1 in neurons and astrocytes and (iii) a strong increase in Glyoxalase 1 dimers after neuronal injury (24 hours to 72 hours) when compared to monomers of the protein. CONCLUSIONS: The high dynamics of Glyoxalase 1 expression and distribution following neuronal injury may indicate a novel role of Glyoxalase 1.
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spelling pubmed-39119452014-02-04 Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury Pieroh, Philipp Koch, Marco Wagner, Daniel-Christoph Boltze, Johannes Ehrlich, Angela Ghadban, Chalid Hobusch, Constance Birkenmeier, Gerd Dehghani, Faramarz PLoS One Research Article BACKGROUND: Enhanced glycolysis leads to elevated levels of the toxic metabolite methylglyoxal which contributes to loss of protein-function, metabolic imbalance and cell death. Neurons were shown being highly susceptible to methylglyoxal toxicity. Glyoxalase 1 as an ubiquitous enzyme reflects the main detoxifying enzyme of methylglyoxal and underlies changes during aging and neurodegeneration. However, little is known about dynamics of Glyoxalase 1 following neuronal lesions so far. METHODS: To determine a possible involvement of Glyoxalase 1 in acute brain injury, we analysed the temporal dynamics of Glyoxalase 1 distribution and expression by immunohistochemistry and Western Blot analysis. Organotypic hippocampal slice cultures were excitotoxically (N-methyl-D-aspartate, 50 µM for 4 hours) lesioned in vitro (5 minutes to 72 hours). Additionally, permanent middle cerebral artery occlusion was performed (75 minutes to 60 days). RESULTS: We found (i) a predominant localisation of Glyoxalase 1 in endothelial cells in non-lesioned brains (ii) a time-dependent up-regulation and re-distribution of Glyoxalase 1 in neurons and astrocytes and (iii) a strong increase in Glyoxalase 1 dimers after neuronal injury (24 hours to 72 hours) when compared to monomers of the protein. CONCLUSIONS: The high dynamics of Glyoxalase 1 expression and distribution following neuronal injury may indicate a novel role of Glyoxalase 1. Public Library of Science 2014-02-03 /pmc/articles/PMC3911945/ /pubmed/24498315 http://dx.doi.org/10.1371/journal.pone.0087364 Text en © 2014 Pieroh et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Pieroh, Philipp
Koch, Marco
Wagner, Daniel-Christoph
Boltze, Johannes
Ehrlich, Angela
Ghadban, Chalid
Hobusch, Constance
Birkenmeier, Gerd
Dehghani, Faramarz
Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury
title Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury
title_full Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury
title_fullStr Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury
title_full_unstemmed Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury
title_short Temporal Dynamics of Glyoxalase 1 in Secondary Neuronal Injury
title_sort temporal dynamics of glyoxalase 1 in secondary neuronal injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3911945/
https://www.ncbi.nlm.nih.gov/pubmed/24498315
http://dx.doi.org/10.1371/journal.pone.0087364
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