Cargando…

Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue

Isocitrate dehydrogenase 2 (IDH2) is an NADP(+)-dependent enzyme that catalyzes the oxidative decarboxylation of isocitrate to α-ketoglutarate in the mitochondrial matrix, and is critical for the production of NADPH to limit the accumulation of mitochondrial reactive oxygen species (ROS). Here, we s...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Jae-Ho, Go, Younghoon, Kim, Do-Young, Lee, Sun Hee, Kim, Ok-Hee, Jeon, Yong Hyun, Kwon, Taeg Kyu, Bae, Jae-Hoon, Song, Dae-Kyu, Rhyu, Im Joo, Lee, In-Kyu, Shong, Minho, Oh, Byung-Chul, Petucci, Christopher, Park, Jeen-Woo, Osborne, Timothy F., Im, Seung-Soon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062825/
https://www.ncbi.nlm.nih.gov/pubmed/32015410
http://dx.doi.org/10.1038/s12276-020-0379-z
_version_ 1783504587565563904
author Lee, Jae-Ho
Go, Younghoon
Kim, Do-Young
Lee, Sun Hee
Kim, Ok-Hee
Jeon, Yong Hyun
Kwon, Taeg Kyu
Bae, Jae-Hoon
Song, Dae-Kyu
Rhyu, Im Joo
Lee, In-Kyu
Shong, Minho
Oh, Byung-Chul
Petucci, Christopher
Park, Jeen-Woo
Osborne, Timothy F.
Im, Seung-Soon
author_facet Lee, Jae-Ho
Go, Younghoon
Kim, Do-Young
Lee, Sun Hee
Kim, Ok-Hee
Jeon, Yong Hyun
Kwon, Taeg Kyu
Bae, Jae-Hoon
Song, Dae-Kyu
Rhyu, Im Joo
Lee, In-Kyu
Shong, Minho
Oh, Byung-Chul
Petucci, Christopher
Park, Jeen-Woo
Osborne, Timothy F.
Im, Seung-Soon
author_sort Lee, Jae-Ho
collection PubMed
description Isocitrate dehydrogenase 2 (IDH2) is an NADP(+)-dependent enzyme that catalyzes the oxidative decarboxylation of isocitrate to α-ketoglutarate in the mitochondrial matrix, and is critical for the production of NADPH to limit the accumulation of mitochondrial reactive oxygen species (ROS). Here, we showed that high-fat diet (HFD) feeding resulted in accelerated weight gain in the IDH2KO mice due to a reduction in whole-body energy expenditure. Moreover, the levels of NADP(+), NADPH, NAD(+), and NADH were significantly decreased in the brown adipose tissue (BAT) of the HFD-fed IDH2KO animals, accompanied by decreased mitochondrial function and reduced expression of key genes involved in mitochondrial biogenesis, energy expenditure, and ROS resolution. Interestingly, these changes were partially reversed when the antioxidant butylated hydroxyanisole was added to the HFD. These observations reveal a crucial role for IDH2 in limiting ROS-dependent mitochondrial damage when BAT metabolism is normally enhanced to limit weight gain in response to dietary caloric overload.
format Online
Article
Text
id pubmed-7062825
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Nature Publishing Group UK
record_format MEDLINE/PubMed
spelling pubmed-70628252020-03-18 Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue Lee, Jae-Ho Go, Younghoon Kim, Do-Young Lee, Sun Hee Kim, Ok-Hee Jeon, Yong Hyun Kwon, Taeg Kyu Bae, Jae-Hoon Song, Dae-Kyu Rhyu, Im Joo Lee, In-Kyu Shong, Minho Oh, Byung-Chul Petucci, Christopher Park, Jeen-Woo Osborne, Timothy F. Im, Seung-Soon Exp Mol Med Article Isocitrate dehydrogenase 2 (IDH2) is an NADP(+)-dependent enzyme that catalyzes the oxidative decarboxylation of isocitrate to α-ketoglutarate in the mitochondrial matrix, and is critical for the production of NADPH to limit the accumulation of mitochondrial reactive oxygen species (ROS). Here, we showed that high-fat diet (HFD) feeding resulted in accelerated weight gain in the IDH2KO mice due to a reduction in whole-body energy expenditure. Moreover, the levels of NADP(+), NADPH, NAD(+), and NADH were significantly decreased in the brown adipose tissue (BAT) of the HFD-fed IDH2KO animals, accompanied by decreased mitochondrial function and reduced expression of key genes involved in mitochondrial biogenesis, energy expenditure, and ROS resolution. Interestingly, these changes were partially reversed when the antioxidant butylated hydroxyanisole was added to the HFD. These observations reveal a crucial role for IDH2 in limiting ROS-dependent mitochondrial damage when BAT metabolism is normally enhanced to limit weight gain in response to dietary caloric overload. Nature Publishing Group UK 2020-02-03 /pmc/articles/PMC7062825/ /pubmed/32015410 http://dx.doi.org/10.1038/s12276-020-0379-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Jae-Ho
Go, Younghoon
Kim, Do-Young
Lee, Sun Hee
Kim, Ok-Hee
Jeon, Yong Hyun
Kwon, Taeg Kyu
Bae, Jae-Hoon
Song, Dae-Kyu
Rhyu, Im Joo
Lee, In-Kyu
Shong, Minho
Oh, Byung-Chul
Petucci, Christopher
Park, Jeen-Woo
Osborne, Timothy F.
Im, Seung-Soon
Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
title Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
title_full Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
title_fullStr Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
title_full_unstemmed Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
title_short Isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
title_sort isocitrate dehydrogenase 2 protects mice from high-fat diet-induced metabolic stress by limiting oxidative damage to the mitochondria from brown adipose tissue
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7062825/
https://www.ncbi.nlm.nih.gov/pubmed/32015410
http://dx.doi.org/10.1038/s12276-020-0379-z
work_keys_str_mv AT leejaeho isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT goyounghoon isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT kimdoyoung isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT leesunhee isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT kimokhee isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT jeonyonghyun isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT kwontaegkyu isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT baejaehoon isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT songdaekyu isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT rhyuimjoo isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT leeinkyu isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT shongminho isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT ohbyungchul isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT petuccichristopher isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT parkjeenwoo isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT osbornetimothyf isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue
AT imseungsoon isocitratedehydrogenase2protectsmicefromhighfatdietinducedmetabolicstressbylimitingoxidativedamagetothemitochondriafrombrownadiposetissue