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PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis

OBJECTIVES: Purple potato (PP) is a good dietary source of polyphenol and promotes gut epithelial health. The objective of this study is to examine the impact of PP extract on mitochondrial biogenesis and evaluate the role of peroxisome proliferator-activated receptor gamma coactivator (PGC)-1α in t...

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Autores principales: Sun, Qi, Iniguez, Alejandro Bravo, Tian, Qiyu, Du, Min, Zhu, Mei-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194176/
http://dx.doi.org/10.1093/cdn/nzac077.040
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author Sun, Qi
Iniguez, Alejandro Bravo
Tian, Qiyu
Du, Min
Zhu, Mei-Jun
author_facet Sun, Qi
Iniguez, Alejandro Bravo
Tian, Qiyu
Du, Min
Zhu, Mei-Jun
author_sort Sun, Qi
collection PubMed
description OBJECTIVES: Purple potato (PP) is a good dietary source of polyphenol and promotes gut epithelial health. The objective of this study is to examine the impact of PP extract on mitochondrial biogenesis and evaluate the role of peroxisome proliferator-activated receptor gamma coactivator (PGC)-1α in this. METHODS: In cultured colonic epithelial Caco-2 cells, the effects of PP extract on PGC-1α, cell differentiation, and markers of mitochondrial biogenesis, including mitochondrial DNA content, mitochondrial enzyme gene expression, and levels of metabolic intermediates, were first evaluated. Then, inhibition of PGC-1α induced by either inhibitor SR-18,292 or siRNA-mediated knockdown were used to evaluate its role in PP extract-promoted differentiation and mitochondrial biogenesis. RESULTS: PP extract up-regulated the level of PGC-1α, mitochondrial gene expression, mitochondrial DNA (mtDNA) copy number, and the level of citric acid cycle metabolites in Caco-2 cells. Inhibition of PGC-1α eliminated the enhancing effects of PP extract on the expression of differentiation markers, mitochondrial metabolites and mtDNA content, as well as the mRNA expression of mitochondria-encoded proteins. CONCLUSIONS: PP extract promoted the differentiation of intestinal epithelial cells, mitochondrial biogenesis and oxidative metabolism, which is in a PGC-1α-dependent way. FUNDING SOURCES: United States Department of Agriculture-National Institute of Food and Agriculture (USDA-NIFA) (2018-67,017-27,517) and Washington State University Agricultural Research Center Emerging Research Issues Competitive Grant.
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spelling pubmed-91941762022-06-14 PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis Sun, Qi Iniguez, Alejandro Bravo Tian, Qiyu Du, Min Zhu, Mei-Jun Curr Dev Nutr Food Science and Nutrition OBJECTIVES: Purple potato (PP) is a good dietary source of polyphenol and promotes gut epithelial health. The objective of this study is to examine the impact of PP extract on mitochondrial biogenesis and evaluate the role of peroxisome proliferator-activated receptor gamma coactivator (PGC)-1α in this. METHODS: In cultured colonic epithelial Caco-2 cells, the effects of PP extract on PGC-1α, cell differentiation, and markers of mitochondrial biogenesis, including mitochondrial DNA content, mitochondrial enzyme gene expression, and levels of metabolic intermediates, were first evaluated. Then, inhibition of PGC-1α induced by either inhibitor SR-18,292 or siRNA-mediated knockdown were used to evaluate its role in PP extract-promoted differentiation and mitochondrial biogenesis. RESULTS: PP extract up-regulated the level of PGC-1α, mitochondrial gene expression, mitochondrial DNA (mtDNA) copy number, and the level of citric acid cycle metabolites in Caco-2 cells. Inhibition of PGC-1α eliminated the enhancing effects of PP extract on the expression of differentiation markers, mitochondrial metabolites and mtDNA content, as well as the mRNA expression of mitochondria-encoded proteins. CONCLUSIONS: PP extract promoted the differentiation of intestinal epithelial cells, mitochondrial biogenesis and oxidative metabolism, which is in a PGC-1α-dependent way. FUNDING SOURCES: United States Department of Agriculture-National Institute of Food and Agriculture (USDA-NIFA) (2018-67,017-27,517) and Washington State University Agricultural Research Center Emerging Research Issues Competitive Grant. Oxford University Press 2022-06-14 /pmc/articles/PMC9194176/ http://dx.doi.org/10.1093/cdn/nzac077.040 Text en © The Author 2022. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology. 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 (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Food Science and Nutrition
Sun, Qi
Iniguez, Alejandro Bravo
Tian, Qiyu
Du, Min
Zhu, Mei-Jun
PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis
title PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis
title_full PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis
title_fullStr PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis
title_full_unstemmed PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis
title_short PGC-1α Is Indispensable in Purple Potato Promoted Intestinal Epithelial Differentiation and Mitochondrial Biogenesis
title_sort pgc-1α is indispensable in purple potato promoted intestinal epithelial differentiation and mitochondrial biogenesis
topic Food Science and Nutrition
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9194176/
http://dx.doi.org/10.1093/cdn/nzac077.040
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