Acetylation in Mitochondria Dynamics and Neurodegeneration
Mitochondria are a unique intracellular organelle due to their evolutionary origin and multifunctional role in overall cellular physiology and pathophysiology. To meet the specific spatial metabolic demands within the cell, mitochondria are actively moving, dividing, or fusing. This process of mitoc...
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MDPI AG
2021
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oai:doaj.org-article:3bf7250e26d9477ca2981d5b5f5f88f22021-11-25T17:10:34ZAcetylation in Mitochondria Dynamics and Neurodegeneration10.3390/cells101130312073-4409https://doaj.org/article/3bf7250e26d9477ca2981d5b5f5f88f22021-11-01T00:00:00Zhttps://www.mdpi.com/2073-4409/10/11/3031https://doaj.org/toc/2073-4409Mitochondria are a unique intracellular organelle due to their evolutionary origin and multifunctional role in overall cellular physiology and pathophysiology. To meet the specific spatial metabolic demands within the cell, mitochondria are actively moving, dividing, or fusing. This process of mitochondrial dynamics is fine-tuned by a specific group of proteins and their complex post-translational modifications. In this review, we discuss the mitochondrial dynamics regulatory enzymes, their adaptor proteins, and the effect of acetylation on the activity of fusion and fission machinery as a ubiquitous response to metabolic stresses. Further, we discuss the role of intracellular cytoskeleton structures and their post-translational modifications in the modulation of mitochondrial fusion and fission. Finally, we review the role of mitochondrial dynamics dysregulation in the pathophysiology of acute brain injury and the treatment strategies based on modulation of NAD<sup>+</sup>-dependent deacetylation.Jaylyn WaddellAditi BanerjeeTibor KristianMDPI AGarticlemitochondriadynamicstubulinacetylationBiology (General)QH301-705.5ENCells, Vol 10, Iss 3031, p 3031 (2021) |
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mitochondria dynamics tubulin acetylation Biology (General) QH301-705.5 |
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mitochondria dynamics tubulin acetylation Biology (General) QH301-705.5 Jaylyn Waddell Aditi Banerjee Tibor Kristian Acetylation in Mitochondria Dynamics and Neurodegeneration |
description |
Mitochondria are a unique intracellular organelle due to their evolutionary origin and multifunctional role in overall cellular physiology and pathophysiology. To meet the specific spatial metabolic demands within the cell, mitochondria are actively moving, dividing, or fusing. This process of mitochondrial dynamics is fine-tuned by a specific group of proteins and their complex post-translational modifications. In this review, we discuss the mitochondrial dynamics regulatory enzymes, their adaptor proteins, and the effect of acetylation on the activity of fusion and fission machinery as a ubiquitous response to metabolic stresses. Further, we discuss the role of intracellular cytoskeleton structures and their post-translational modifications in the modulation of mitochondrial fusion and fission. Finally, we review the role of mitochondrial dynamics dysregulation in the pathophysiology of acute brain injury and the treatment strategies based on modulation of NAD<sup>+</sup>-dependent deacetylation. |
format |
article |
author |
Jaylyn Waddell Aditi Banerjee Tibor Kristian |
author_facet |
Jaylyn Waddell Aditi Banerjee Tibor Kristian |
author_sort |
Jaylyn Waddell |
title |
Acetylation in Mitochondria Dynamics and Neurodegeneration |
title_short |
Acetylation in Mitochondria Dynamics and Neurodegeneration |
title_full |
Acetylation in Mitochondria Dynamics and Neurodegeneration |
title_fullStr |
Acetylation in Mitochondria Dynamics and Neurodegeneration |
title_full_unstemmed |
Acetylation in Mitochondria Dynamics and Neurodegeneration |
title_sort |
acetylation in mitochondria dynamics and neurodegeneration |
publisher |
MDPI AG |
publishDate |
2021 |
url |
https://doaj.org/article/3bf7250e26d9477ca2981d5b5f5f88f2 |
work_keys_str_mv |
AT jaylynwaddell acetylationinmitochondriadynamicsandneurodegeneration AT aditibanerjee acetylationinmitochondriadynamicsandneurodegeneration AT tiborkristian acetylationinmitochondriadynamicsandneurodegeneration |
_version_ |
1718412641954693120 |