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VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases
The voltage-dependent anion channel 1 (VDAC1) protein, is an important regulator of mitochondrial function, and serves as a mitochondrial gatekeeper, with responsibility for cellular fate. In addition to control over energy sources and metabolism, the protein also regulates epigenomic elements and a...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693975/ https://www.ncbi.nlm.nih.gov/pubmed/33114780 http://dx.doi.org/10.3390/biom10111485 |
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author | Shoshan-Barmatz, Varda Shteinfer-Kuzmine, Anna Verma, Ankit |
author_facet | Shoshan-Barmatz, Varda Shteinfer-Kuzmine, Anna Verma, Ankit |
author_sort | Shoshan-Barmatz, Varda |
collection | PubMed |
description | The voltage-dependent anion channel 1 (VDAC1) protein, is an important regulator of mitochondrial function, and serves as a mitochondrial gatekeeper, with responsibility for cellular fate. In addition to control over energy sources and metabolism, the protein also regulates epigenomic elements and apoptosis via mediating the release of apoptotic proteins from the mitochondria. Apoptotic and pathological conditions, as well as certain viruses, induce cell death by inducing VDAC1 overexpression leading to oligomerization, and the formation of a large channel within the VDAC1 homo-oligomer. This then permits the release of pro-apoptotic proteins from the mitochondria and subsequent apoptosis. Mitochondrial DNA can also be released through this channel, which triggers type-Ι interferon responses. VDAC1 also participates in endoplasmic reticulum (ER)-mitochondria cross-talk, and in the regulation of autophagy, and inflammation. Its location in the outer mitochondrial membrane, makes VDAC1 ideally placed to interact with over 100 proteins, and to orchestrate the interaction of mitochondrial and cellular activities through a number of signaling pathways. Here, we provide insights into the multiple functions of VDAC1 and describe its involvement in several diseases, which demonstrate the potential of this protein as a druggable target in a wide variety of pathologies, including cancer. |
format | Online Article Text |
id | pubmed-7693975 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76939752020-11-28 VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases Shoshan-Barmatz, Varda Shteinfer-Kuzmine, Anna Verma, Ankit Biomolecules Review The voltage-dependent anion channel 1 (VDAC1) protein, is an important regulator of mitochondrial function, and serves as a mitochondrial gatekeeper, with responsibility for cellular fate. In addition to control over energy sources and metabolism, the protein also regulates epigenomic elements and apoptosis via mediating the release of apoptotic proteins from the mitochondria. Apoptotic and pathological conditions, as well as certain viruses, induce cell death by inducing VDAC1 overexpression leading to oligomerization, and the formation of a large channel within the VDAC1 homo-oligomer. This then permits the release of pro-apoptotic proteins from the mitochondria and subsequent apoptosis. Mitochondrial DNA can also be released through this channel, which triggers type-Ι interferon responses. VDAC1 also participates in endoplasmic reticulum (ER)-mitochondria cross-talk, and in the regulation of autophagy, and inflammation. Its location in the outer mitochondrial membrane, makes VDAC1 ideally placed to interact with over 100 proteins, and to orchestrate the interaction of mitochondrial and cellular activities through a number of signaling pathways. Here, we provide insights into the multiple functions of VDAC1 and describe its involvement in several diseases, which demonstrate the potential of this protein as a druggable target in a wide variety of pathologies, including cancer. MDPI 2020-10-26 /pmc/articles/PMC7693975/ /pubmed/33114780 http://dx.doi.org/10.3390/biom10111485 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 Shoshan-Barmatz, Varda Shteinfer-Kuzmine, Anna Verma, Ankit VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases |
title | VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases |
title_full | VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases |
title_fullStr | VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases |
title_full_unstemmed | VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases |
title_short | VDAC1 at the Intersection of Cell Metabolism, Apoptosis, and Diseases |
title_sort | vdac1 at the intersection of cell metabolism, apoptosis, and diseases |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7693975/ https://www.ncbi.nlm.nih.gov/pubmed/33114780 http://dx.doi.org/10.3390/biom10111485 |
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