Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity

Age-related impairment of mitochondrial function may negatively impact energy-demanding processes such as synaptic transmission thereby triggering cognitive decline and processes of neurodegeneration. Here, we present a novel model for age-related mitochondrial impairment based on partial inhibition...

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Main Authors: Martin Kriebel, Julia Ebel, Florian Battke, Stefan Griesbach, Hansjürgen Volkmer
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-03-01
Series:Frontiers in Molecular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnmol.2020.00043/full
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spelling doaj-64e6ba53041a488cb24257eae7a97c6b2020-11-25T01:58:54ZengFrontiers Media S.A.Frontiers in Molecular Neuroscience1662-50992020-03-011310.3389/fnmol.2020.00043514656Interference With Complex IV as a Model of Age-Related Decline in Synaptic ConnectivityMartin Kriebel0Julia Ebel1Florian Battke2Stefan Griesbach3Hansjürgen Volkmer4Department of Molecular Biology and Neurobiology, NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, GermanyDepartment of Molecular Biology and Neurobiology, NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, GermanyCeGaT GmbH, Tübingen, GermanyCeGaT GmbH, Tübingen, GermanyDepartment of Molecular Biology and Neurobiology, NMI Natural and Medical Sciences Institute at the University of Tübingen, Reutlingen, GermanyAge-related impairment of mitochondrial function may negatively impact energy-demanding processes such as synaptic transmission thereby triggering cognitive decline and processes of neurodegeneration. Here, we present a novel model for age-related mitochondrial impairment based on partial inhibition of cytochrome c oxidase subunit 4 (Cox4) of complex IV of the respiratory chain. miRNA-mediated knockdown of Cox4 correlated with a marked reduction in excitatory and inhibitory synaptic marker densities in vitro and in vivo as well as an impairment of neuronal network activity in primary neuronal cultures. Transcriptome analysis identified the deregulation of gene clusters, which link induced mitochondrial perturbation to impaired synaptic function and plasticity as well as processes of aging. In conclusion, the model of Cox4 deficiency reflects aspects of age-related dementia and might, therefore, serve as a novel test system for drug development.https://www.frontiersin.org/article/10.3389/fnmol.2020.00043/fullcytochrome c oxidaseCox4mitochondriaagingsynaptic connectivityneurodegeneration
collection DOAJ
language English
format Article
sources DOAJ
author Martin Kriebel
Julia Ebel
Florian Battke
Stefan Griesbach
Hansjürgen Volkmer
spellingShingle Martin Kriebel
Julia Ebel
Florian Battke
Stefan Griesbach
Hansjürgen Volkmer
Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity
Frontiers in Molecular Neuroscience
cytochrome c oxidase
Cox4
mitochondria
aging
synaptic connectivity
neurodegeneration
author_facet Martin Kriebel
Julia Ebel
Florian Battke
Stefan Griesbach
Hansjürgen Volkmer
author_sort Martin Kriebel
title Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity
title_short Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity
title_full Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity
title_fullStr Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity
title_full_unstemmed Interference With Complex IV as a Model of Age-Related Decline in Synaptic Connectivity
title_sort interference with complex iv as a model of age-related decline in synaptic connectivity
publisher Frontiers Media S.A.
series Frontiers in Molecular Neuroscience
issn 1662-5099
publishDate 2020-03-01
description Age-related impairment of mitochondrial function may negatively impact energy-demanding processes such as synaptic transmission thereby triggering cognitive decline and processes of neurodegeneration. Here, we present a novel model for age-related mitochondrial impairment based on partial inhibition of cytochrome c oxidase subunit 4 (Cox4) of complex IV of the respiratory chain. miRNA-mediated knockdown of Cox4 correlated with a marked reduction in excitatory and inhibitory synaptic marker densities in vitro and in vivo as well as an impairment of neuronal network activity in primary neuronal cultures. Transcriptome analysis identified the deregulation of gene clusters, which link induced mitochondrial perturbation to impaired synaptic function and plasticity as well as processes of aging. In conclusion, the model of Cox4 deficiency reflects aspects of age-related dementia and might, therefore, serve as a novel test system for drug development.
topic cytochrome c oxidase
Cox4
mitochondria
aging
synaptic connectivity
neurodegeneration
url https://www.frontiersin.org/article/10.3389/fnmol.2020.00043/full
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