Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.

Our objective was to investigate the mitochondrial dynamics following oxygen-glucose deprivation (OGD) in cultured rat cortical neurons. We documented changes in morphology, protein expression, and DNA levels in mitochondria following OGD and examined the roles of mitochondrial fission [dynamin-rela...

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Main Authors: Edina A Wappler, Adam Institoris, Somhrita Dutta, Prasad V G Katakam, David W Busija
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3642144?pdf=render
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spelling doaj-f90e92b304e24f7087fefeabd750d57f2020-11-25T02:30:59ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0185e6320610.1371/journal.pone.0063206Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.Edina A WapplerAdam InstitorisSomhrita DuttaPrasad V G KatakamDavid W BusijaOur objective was to investigate the mitochondrial dynamics following oxygen-glucose deprivation (OGD) in cultured rat cortical neurons. We documented changes in morphology, protein expression, and DNA levels in mitochondria following OGD and examined the roles of mitochondrial fission [dynamin-related protein 1 (Drp1), fission protein-1 (Fis1)] and fusion [mitofusin-1 (Mfn1), mitofusin-2 (Mfn2), and optic atrophy-1 protein (OPA1)] proteins on mitochondrial biogenesis and morphogenesis. We tested the effects of two Drp1 blockers [15-deoxy-Δ12,14-Prostaglandin J2 (PGJ2) and Mitochondrial Division Inhibitor (Mdivi-1)] on mitochondrial dynamics and cell survival. One hour of OGD had minimal effects on neuronal viability but mitochondria appeared condensed. Three hours of OGD caused a 60% decrease in neuronal viability accompanied by a transition from primarily normal/tubular and lesser number of rounded mitochondria during normoxia to either poorly labeled or small and large rounded mitochondria. The percentage of rounded mitochondria remained the same. The mitochondrial voltage-dependent anion channel, Complex V, and mitoDNA levels increased after OGD associated with a dramatic reduction in Drp1 expression, less reduction in Mfn2 expression, an increase in Mfn1 expression, with no changes in either OPA1 or Fis1. Although PGJ2 increased polymerization of Drp1, it did not reduce cell death or alter mitochondrial morphology following OGD and Mdivi-1 did not protect neurons against OGD. In summary, mitochondrial biogenesis and maintained fusion occurred in neurons along with mitochondrial fission following OGD; thus Mfn1 but not Drp1 may be a major regulator of these processes.http://europepmc.org/articles/PMC3642144?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Edina A Wappler
Adam Institoris
Somhrita Dutta
Prasad V G Katakam
David W Busija
spellingShingle Edina A Wappler
Adam Institoris
Somhrita Dutta
Prasad V G Katakam
David W Busija
Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
PLoS ONE
author_facet Edina A Wappler
Adam Institoris
Somhrita Dutta
Prasad V G Katakam
David W Busija
author_sort Edina A Wappler
title Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
title_short Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
title_full Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
title_fullStr Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
title_full_unstemmed Mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
title_sort mitochondrial dynamics associated with oxygen-glucose deprivation in rat primary neuronal cultures.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Our objective was to investigate the mitochondrial dynamics following oxygen-glucose deprivation (OGD) in cultured rat cortical neurons. We documented changes in morphology, protein expression, and DNA levels in mitochondria following OGD and examined the roles of mitochondrial fission [dynamin-related protein 1 (Drp1), fission protein-1 (Fis1)] and fusion [mitofusin-1 (Mfn1), mitofusin-2 (Mfn2), and optic atrophy-1 protein (OPA1)] proteins on mitochondrial biogenesis and morphogenesis. We tested the effects of two Drp1 blockers [15-deoxy-Δ12,14-Prostaglandin J2 (PGJ2) and Mitochondrial Division Inhibitor (Mdivi-1)] on mitochondrial dynamics and cell survival. One hour of OGD had minimal effects on neuronal viability but mitochondria appeared condensed. Three hours of OGD caused a 60% decrease in neuronal viability accompanied by a transition from primarily normal/tubular and lesser number of rounded mitochondria during normoxia to either poorly labeled or small and large rounded mitochondria. The percentage of rounded mitochondria remained the same. The mitochondrial voltage-dependent anion channel, Complex V, and mitoDNA levels increased after OGD associated with a dramatic reduction in Drp1 expression, less reduction in Mfn2 expression, an increase in Mfn1 expression, with no changes in either OPA1 or Fis1. Although PGJ2 increased polymerization of Drp1, it did not reduce cell death or alter mitochondrial morphology following OGD and Mdivi-1 did not protect neurons against OGD. In summary, mitochondrial biogenesis and maintained fusion occurred in neurons along with mitochondrial fission following OGD; thus Mfn1 but not Drp1 may be a major regulator of these processes.
url http://europepmc.org/articles/PMC3642144?pdf=render
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