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Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons

Mitochondrial dynamics and mitophagy are constitutive and complex systems that ensure a healthy mitochondrial network through the segregation and subsequent degradation of damaged mitochondria. Disruption of these systems can lead to mitochondrial dysfunction and has been established as a central me...

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Autores principales: Anzell, Anthony R., Fogo, Garrett M., Gurm, Zoya, Raghunayakula, Sarita, Wider, Joseph M., Maheras, Kathleen J., Emaus, Katlynn J., Bryson, Timothy D., Wang, Madison, Neumar, Robert W., Przyklenk, Karin, Sanderson, Thomas H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115279/
https://www.ncbi.nlm.nih.gov/pubmed/33980811
http://dx.doi.org/10.1038/s41419-021-03752-2
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author Anzell, Anthony R.
Fogo, Garrett M.
Gurm, Zoya
Raghunayakula, Sarita
Wider, Joseph M.
Maheras, Kathleen J.
Emaus, Katlynn J.
Bryson, Timothy D.
Wang, Madison
Neumar, Robert W.
Przyklenk, Karin
Sanderson, Thomas H.
author_facet Anzell, Anthony R.
Fogo, Garrett M.
Gurm, Zoya
Raghunayakula, Sarita
Wider, Joseph M.
Maheras, Kathleen J.
Emaus, Katlynn J.
Bryson, Timothy D.
Wang, Madison
Neumar, Robert W.
Przyklenk, Karin
Sanderson, Thomas H.
author_sort Anzell, Anthony R.
collection PubMed
description Mitochondrial dynamics and mitophagy are constitutive and complex systems that ensure a healthy mitochondrial network through the segregation and subsequent degradation of damaged mitochondria. Disruption of these systems can lead to mitochondrial dysfunction and has been established as a central mechanism of ischemia/reperfusion (I/R) injury. Emerging evidence suggests that mitochondrial dynamics and mitophagy are integrated systems; however, the role of this relationship in the context of I/R injury remains unclear. To investigate this concept, we utilized primary cortical neurons isolated from the novel dual-reporter mitochondrial quality control knockin mice (C57BL/6-Gt(ROSA)26Sortm1(CAG-mCherry/GFP)Ganl/J) with conditional knockout (KO) of Drp1 to investigate changes in mitochondrial dynamics and mitophagic flux during in vitro I/R injury. Mitochondrial dynamics was quantitatively measured in an unbiased manner using a machine learning mitochondrial morphology classification system, which consisted of four different classifications: network, unbranched, swollen, and punctate. Evaluation of mitochondrial morphology and mitophagic flux in primary neurons exposed to oxygen-glucose deprivation (OGD) and reoxygenation (OGD/R) revealed extensive mitochondrial fragmentation and swelling, together with a significant upregulation in mitophagic flux. Furthermore, the primary morphology of mitochondria undergoing mitophagy was classified as punctate. Colocalization using immunofluorescence as well as western blot analysis revealed that the PINK1/Parkin pathway of mitophagy was activated following OGD/R. Conditional KO of Drp1 prevented mitochondrial fragmentation and swelling following OGD/R but did not alter mitophagic flux. These data provide novel evidence that Drp1 plays a causal role in the progression of I/R injury, but mitophagy does not require Drp1-mediated mitochondrial fission.
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spelling pubmed-81152792021-05-12 Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons Anzell, Anthony R. Fogo, Garrett M. Gurm, Zoya Raghunayakula, Sarita Wider, Joseph M. Maheras, Kathleen J. Emaus, Katlynn J. Bryson, Timothy D. Wang, Madison Neumar, Robert W. Przyklenk, Karin Sanderson, Thomas H. Cell Death Dis Article Mitochondrial dynamics and mitophagy are constitutive and complex systems that ensure a healthy mitochondrial network through the segregation and subsequent degradation of damaged mitochondria. Disruption of these systems can lead to mitochondrial dysfunction and has been established as a central mechanism of ischemia/reperfusion (I/R) injury. Emerging evidence suggests that mitochondrial dynamics and mitophagy are integrated systems; however, the role of this relationship in the context of I/R injury remains unclear. To investigate this concept, we utilized primary cortical neurons isolated from the novel dual-reporter mitochondrial quality control knockin mice (C57BL/6-Gt(ROSA)26Sortm1(CAG-mCherry/GFP)Ganl/J) with conditional knockout (KO) of Drp1 to investigate changes in mitochondrial dynamics and mitophagic flux during in vitro I/R injury. Mitochondrial dynamics was quantitatively measured in an unbiased manner using a machine learning mitochondrial morphology classification system, which consisted of four different classifications: network, unbranched, swollen, and punctate. Evaluation of mitochondrial morphology and mitophagic flux in primary neurons exposed to oxygen-glucose deprivation (OGD) and reoxygenation (OGD/R) revealed extensive mitochondrial fragmentation and swelling, together with a significant upregulation in mitophagic flux. Furthermore, the primary morphology of mitochondria undergoing mitophagy was classified as punctate. Colocalization using immunofluorescence as well as western blot analysis revealed that the PINK1/Parkin pathway of mitophagy was activated following OGD/R. Conditional KO of Drp1 prevented mitochondrial fragmentation and swelling following OGD/R but did not alter mitophagic flux. These data provide novel evidence that Drp1 plays a causal role in the progression of I/R injury, but mitophagy does not require Drp1-mediated mitochondrial fission. Nature Publishing Group UK 2021-05-12 /pmc/articles/PMC8115279/ /pubmed/33980811 http://dx.doi.org/10.1038/s41419-021-03752-2 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Anzell, Anthony R.
Fogo, Garrett M.
Gurm, Zoya
Raghunayakula, Sarita
Wider, Joseph M.
Maheras, Kathleen J.
Emaus, Katlynn J.
Bryson, Timothy D.
Wang, Madison
Neumar, Robert W.
Przyklenk, Karin
Sanderson, Thomas H.
Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
title Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
title_full Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
title_fullStr Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
title_full_unstemmed Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
title_short Mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
title_sort mitochondrial fission and mitophagy are independent mechanisms regulating ischemia/reperfusion injury in primary neurons
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115279/
https://www.ncbi.nlm.nih.gov/pubmed/33980811
http://dx.doi.org/10.1038/s41419-021-03752-2
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