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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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 |
work_keys_str_mv |
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