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Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure

BACKGROUND: In complex congenital heart disease patients such as those with tetralogy of Fallot, the right ventricle (RV) is subject to pressure overload, leading to RV hypertrophy and eventually RV failure. The mechanisms that promote the transition from stable RV hypertrophy to RV failure are unkn...

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Autores principales: Hwang, HyunTae V., Sandeep, Nefthi, Nair, Ramesh V., Hu, Dong‐Qing, Zhao, Mingming, Lan, Ingrid S., Fajardo, Giovanni, Matkovich, Scot J., Bernstein, Daniel, Reddy, Sushma
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955345/
https://www.ncbi.nlm.nih.gov/pubmed/33522250
http://dx.doi.org/10.1161/JAHA.120.017835
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author Hwang, HyunTae V.
Sandeep, Nefthi
Nair, Ramesh V.
Hu, Dong‐Qing
Zhao, Mingming
Lan, Ingrid S.
Fajardo, Giovanni
Matkovich, Scot J.
Bernstein, Daniel
Reddy, Sushma
author_facet Hwang, HyunTae V.
Sandeep, Nefthi
Nair, Ramesh V.
Hu, Dong‐Qing
Zhao, Mingming
Lan, Ingrid S.
Fajardo, Giovanni
Matkovich, Scot J.
Bernstein, Daniel
Reddy, Sushma
author_sort Hwang, HyunTae V.
collection PubMed
description BACKGROUND: In complex congenital heart disease patients such as those with tetralogy of Fallot, the right ventricle (RV) is subject to pressure overload, leading to RV hypertrophy and eventually RV failure. The mechanisms that promote the transition from stable RV hypertrophy to RV failure are unknown. We evaluated the role of mitochondrial bioenergetics in the development of RV failure. METHODS AND RESULTS: We created a murine model of RV pressure overload by pulmonary artery banding and compared with sham‐operated controls. Gene expression by RNA‐sequencing, oxidative stress, mitochondrial respiration, dynamics, and structure were assessed in pressure overload‐induced RV failure. RV failure was characterized by decreased expression of electron transport chain genes and mitochondrial antioxidant genes (aldehyde dehydrogenase 2 and superoxide dismutase 2) and increased expression of oxidant stress markers (heme oxygenase, 4‐hydroxynonenal). The activities of all electron transport chain complexes decreased with RV hypertrophy and further with RV failure (oxidative phosphorylation: sham 552.3±43.07 versus RV hypertrophy 334.3±30.65 versus RV failure 165.4±36.72 pmol/(s×mL), P<0.0001). Mitochondrial fission protein DRP1 (dynamin 1‐like) trended toward an increase, while MFF (mitochondrial fission factor) decreased and fusion protein OPA1 (mitochondrial dynamin like GTPase) decreased. In contrast, transcription of electron transport chain genes increased in the left ventricle of RV failure. CONCLUSIONS: Pressure overload‐induced RV failure is characterized by decreased transcription and activity of electron transport chain complexes and increased oxidative stress which are associated with decreased energy generation. An improved understanding of the complex processes of energy generation could aid in developing novel therapies to mitigate mitochondrial dysfunction and delay the onset of RV failure.
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spelling pubmed-79553452021-03-17 Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure Hwang, HyunTae V. Sandeep, Nefthi Nair, Ramesh V. Hu, Dong‐Qing Zhao, Mingming Lan, Ingrid S. Fajardo, Giovanni Matkovich, Scot J. Bernstein, Daniel Reddy, Sushma J Am Heart Assoc Original Research BACKGROUND: In complex congenital heart disease patients such as those with tetralogy of Fallot, the right ventricle (RV) is subject to pressure overload, leading to RV hypertrophy and eventually RV failure. The mechanisms that promote the transition from stable RV hypertrophy to RV failure are unknown. We evaluated the role of mitochondrial bioenergetics in the development of RV failure. METHODS AND RESULTS: We created a murine model of RV pressure overload by pulmonary artery banding and compared with sham‐operated controls. Gene expression by RNA‐sequencing, oxidative stress, mitochondrial respiration, dynamics, and structure were assessed in pressure overload‐induced RV failure. RV failure was characterized by decreased expression of electron transport chain genes and mitochondrial antioxidant genes (aldehyde dehydrogenase 2 and superoxide dismutase 2) and increased expression of oxidant stress markers (heme oxygenase, 4‐hydroxynonenal). The activities of all electron transport chain complexes decreased with RV hypertrophy and further with RV failure (oxidative phosphorylation: sham 552.3±43.07 versus RV hypertrophy 334.3±30.65 versus RV failure 165.4±36.72 pmol/(s×mL), P<0.0001). Mitochondrial fission protein DRP1 (dynamin 1‐like) trended toward an increase, while MFF (mitochondrial fission factor) decreased and fusion protein OPA1 (mitochondrial dynamin like GTPase) decreased. In contrast, transcription of electron transport chain genes increased in the left ventricle of RV failure. CONCLUSIONS: Pressure overload‐induced RV failure is characterized by decreased transcription and activity of electron transport chain complexes and increased oxidative stress which are associated with decreased energy generation. An improved understanding of the complex processes of energy generation could aid in developing novel therapies to mitigate mitochondrial dysfunction and delay the onset of RV failure. John Wiley and Sons Inc. 2021-01-30 /pmc/articles/PMC7955345/ /pubmed/33522250 http://dx.doi.org/10.1161/JAHA.120.017835 Text en © 2021 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Hwang, HyunTae V.
Sandeep, Nefthi
Nair, Ramesh V.
Hu, Dong‐Qing
Zhao, Mingming
Lan, Ingrid S.
Fajardo, Giovanni
Matkovich, Scot J.
Bernstein, Daniel
Reddy, Sushma
Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure
title Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure
title_full Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure
title_fullStr Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure
title_full_unstemmed Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure
title_short Transcriptomic and Functional Analyses of Mitochondrial Dysfunction in Pressure Overload‐Induced Right Ventricular Failure
title_sort transcriptomic and functional analyses of mitochondrial dysfunction in pressure overload‐induced right ventricular failure
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7955345/
https://www.ncbi.nlm.nih.gov/pubmed/33522250
http://dx.doi.org/10.1161/JAHA.120.017835
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