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Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases

Mitochondria are complex metabolic organelles with manifold pathophysiological implications in diabetes. Currently published mitochondrial-encoded peptides, which are expressed from the mitochondrial open reading frame of the 12S ribosomal RNA type-c (MOTS-c), 16S rRNA (humanin and short humanin lik...

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Detalles Bibliográficos
Autores principales: Kong, Byung Soo, Lee, Changhan, Cho, Young Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Diabetes Association 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244198/
https://www.ncbi.nlm.nih.gov/pubmed/36824008
http://dx.doi.org/10.4093/dmj.2022.0333
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author Kong, Byung Soo
Lee, Changhan
Cho, Young Min
author_facet Kong, Byung Soo
Lee, Changhan
Cho, Young Min
author_sort Kong, Byung Soo
collection PubMed
description Mitochondria are complex metabolic organelles with manifold pathophysiological implications in diabetes. Currently published mitochondrial-encoded peptides, which are expressed from the mitochondrial open reading frame of the 12S ribosomal RNA type-c (MOTS-c), 16S rRNA (humanin and short humanin like peptide 1-6 [SHLP1-6]), or small human mitochondrial open reading frame over serine tRNA (SHMOOSE) are associated with regulation of cellular metabolism and insulin action in age-related diseases, such as type 2 diabetes mellitus. This review focuses mainly on recent advances in MOTS-c research with regards to diabetes, including both type 1 and type 2. The emerging understanding of MOTS-c in diabetes may provide insight into the development of new therapies for diabetes and other age or senescence-related diseases.
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spelling pubmed-102441982023-06-08 Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases Kong, Byung Soo Lee, Changhan Cho, Young Min Diabetes Metab J Review Mitochondria are complex metabolic organelles with manifold pathophysiological implications in diabetes. Currently published mitochondrial-encoded peptides, which are expressed from the mitochondrial open reading frame of the 12S ribosomal RNA type-c (MOTS-c), 16S rRNA (humanin and short humanin like peptide 1-6 [SHLP1-6]), or small human mitochondrial open reading frame over serine tRNA (SHMOOSE) are associated with regulation of cellular metabolism and insulin action in age-related diseases, such as type 2 diabetes mellitus. This review focuses mainly on recent advances in MOTS-c research with regards to diabetes, including both type 1 and type 2. The emerging understanding of MOTS-c in diabetes may provide insight into the development of new therapies for diabetes and other age or senescence-related diseases. Korean Diabetes Association 2023-05 2023-02-24 /pmc/articles/PMC10244198/ /pubmed/36824008 http://dx.doi.org/10.4093/dmj.2022.0333 Text en Copyright © 2023 Korean Diabetes Association https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Kong, Byung Soo
Lee, Changhan
Cho, Young Min
Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases
title Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases
title_full Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases
title_fullStr Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases
title_full_unstemmed Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases
title_short Mitochondrial-Encoded Peptide MOTS-c, Diabetes, and Aging-Related Diseases
title_sort mitochondrial-encoded peptide mots-c, diabetes, and aging-related diseases
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244198/
https://www.ncbi.nlm.nih.gov/pubmed/36824008
http://dx.doi.org/10.4093/dmj.2022.0333
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