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Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease

Mitochondria are dynamic organelles that undergo constant fission and fusion. Mitochondria dysfunction underlies several human disorders, including Alzheimer’s disease (AD). Preservation of mitochondrial dynamics is fundamental for regulating the organelle’s functions. Several proteins participate i...

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Autores principales: Sita, Giulia, Hrelia, Patrizia, Graziosi, Agnese, Morroni, Fabiana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019958/
https://www.ncbi.nlm.nih.gov/pubmed/31906578
http://dx.doi.org/10.3390/jcm9010126
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author Sita, Giulia
Hrelia, Patrizia
Graziosi, Agnese
Morroni, Fabiana
author_facet Sita, Giulia
Hrelia, Patrizia
Graziosi, Agnese
Morroni, Fabiana
author_sort Sita, Giulia
collection PubMed
description Mitochondria are dynamic organelles that undergo constant fission and fusion. Mitochondria dysfunction underlies several human disorders, including Alzheimer’s disease (AD). Preservation of mitochondrial dynamics is fundamental for regulating the organelle’s functions. Several proteins participate in the regulation of mitochondrial morphology and networks, and among these, Mitofusin 2 (Mfn2) has been extensively studied. This review focuses on the role of Mfn2 in mitochondrial dynamics and in the crosstalk between mitochondria and the endoplasmic reticulum, in particular in AD. Understanding how this protein may be related to AD pathogenesis will provide essential information for the development of therapies for diseases linked to disturbed mitochondrial dynamics, as in AD.
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spelling pubmed-70199582020-03-09 Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease Sita, Giulia Hrelia, Patrizia Graziosi, Agnese Morroni, Fabiana J Clin Med Review Mitochondria are dynamic organelles that undergo constant fission and fusion. Mitochondria dysfunction underlies several human disorders, including Alzheimer’s disease (AD). Preservation of mitochondrial dynamics is fundamental for regulating the organelle’s functions. Several proteins participate in the regulation of mitochondrial morphology and networks, and among these, Mitofusin 2 (Mfn2) has been extensively studied. This review focuses on the role of Mfn2 in mitochondrial dynamics and in the crosstalk between mitochondria and the endoplasmic reticulum, in particular in AD. Understanding how this protein may be related to AD pathogenesis will provide essential information for the development of therapies for diseases linked to disturbed mitochondrial dynamics, as in AD. MDPI 2020-01-02 /pmc/articles/PMC7019958/ /pubmed/31906578 http://dx.doi.org/10.3390/jcm9010126 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Sita, Giulia
Hrelia, Patrizia
Graziosi, Agnese
Morroni, Fabiana
Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease
title Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease
title_full Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease
title_fullStr Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease
title_full_unstemmed Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease
title_short Back to The Fusion: Mitofusin-2 in Alzheimer’s Disease
title_sort back to the fusion: mitofusin-2 in alzheimer’s disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7019958/
https://www.ncbi.nlm.nih.gov/pubmed/31906578
http://dx.doi.org/10.3390/jcm9010126
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