Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart

Abstract Inflammation and a metabolic shift from oxidative metabolism to glycolysis are common in the ischemic heart, the latter partly controlled by pyruvate kinase (muscle, PKM). We previously identified alternative splicing promoting the PKM2 isoform after myocardial infarction (MI). We examined...

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Main Authors: Katie C. Y. Lee, Allison L. Williams, Akitoshi Hara, Vedbar S. Khadka, Jeffrey Hayashi, Ralph V. Shohet
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Physiological Reports
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Online Access:https://doi.org/10.14814/phy2.70193
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author Katie C. Y. Lee
Allison L. Williams
Akitoshi Hara
Vedbar S. Khadka
Jeffrey Hayashi
Ralph V. Shohet
author_facet Katie C. Y. Lee
Allison L. Williams
Akitoshi Hara
Vedbar S. Khadka
Jeffrey Hayashi
Ralph V. Shohet
author_sort Katie C. Y. Lee
collection DOAJ
description Abstract Inflammation and a metabolic shift from oxidative metabolism to glycolysis are common in the ischemic heart, the latter partly controlled by pyruvate kinase (muscle, PKM). We previously identified alternative splicing promoting the PKM2 isoform after myocardial infarction (MI). We examined the role of PKM2 physiological upregulation after MI, modeled by ligation of the left anterior descending coronary artery, using global PKM2 knockout (PKM2−/−) mice. Echocardiography showed similar cardiac function between PKM2−/− and control mice after MI. However, PKM2−/− infarcted hearts had increased abundances of transcripts associated with oxidative stress and immune responses. Immunohistochemistry revealed greater abundance of macrophages in PKM2−/− hearts prior to MI, with a small increase in CD86+ macrophages in PKM2−/− infarcted hearts. Elevated baseline plasma IL‐6, IL‐1β, and C‐reactive protein, and cardiac IL‐6, 3 days post‐MI, were observed in PKM2−/− mice. Oxidative lipid products were also elevated in baseline PKM2−/− hearts, while antioxidant glutathione peroxidase 4 was reduced. Greater fibrosis was seen in PKM2−/− hearts 28 days after MI. These findings suggest Pkm2 ablation primes the heart for increased oxidative stress, inflammation, and fibrosis post‐MI. The natural upregulation of PKM2 may mitigate fibrosis by reducing oxidative stress and inflammation, highlighting its protective role in the infarcted heart.
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spelling doaj-art-ca6208af6f8b401a98c21da7f45976212025-08-20T02:59:35ZengWileyPhysiological Reports2051-817X2025-01-01131n/an/a10.14814/phy2.70193Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heartKatie C. Y. Lee0Allison L. Williams1Akitoshi Hara2Vedbar S. Khadka3Jeffrey Hayashi4Ralph V. Shohet5Department of Medicine, John A. Burns School of Medicine University of Hawaii Mānoa Honolulu Hawaii USADepartment of Medicine, John A. Burns School of Medicine University of Hawaii Mānoa Honolulu Hawaii USADepartment of Medicine, John A. Burns School of Medicine University of Hawaii Mānoa Honolulu Hawaii USABioinformatics Core, Department of Quantitative Health Sciences, John A. Burns School of Medicine University of Hawaii Mānoa Honolulu Hawaii USAJohn A. Burns School of Medicine University of Hawaii Mānoa Honolulu Hawaii USADepartment of Medicine, John A. Burns School of Medicine University of Hawaii Mānoa Honolulu Hawaii USAAbstract Inflammation and a metabolic shift from oxidative metabolism to glycolysis are common in the ischemic heart, the latter partly controlled by pyruvate kinase (muscle, PKM). We previously identified alternative splicing promoting the PKM2 isoform after myocardial infarction (MI). We examined the role of PKM2 physiological upregulation after MI, modeled by ligation of the left anterior descending coronary artery, using global PKM2 knockout (PKM2−/−) mice. Echocardiography showed similar cardiac function between PKM2−/− and control mice after MI. However, PKM2−/− infarcted hearts had increased abundances of transcripts associated with oxidative stress and immune responses. Immunohistochemistry revealed greater abundance of macrophages in PKM2−/− hearts prior to MI, with a small increase in CD86+ macrophages in PKM2−/− infarcted hearts. Elevated baseline plasma IL‐6, IL‐1β, and C‐reactive protein, and cardiac IL‐6, 3 days post‐MI, were observed in PKM2−/− mice. Oxidative lipid products were also elevated in baseline PKM2−/− hearts, while antioxidant glutathione peroxidase 4 was reduced. Greater fibrosis was seen in PKM2−/− hearts 28 days after MI. These findings suggest Pkm2 ablation primes the heart for increased oxidative stress, inflammation, and fibrosis post‐MI. The natural upregulation of PKM2 may mitigate fibrosis by reducing oxidative stress and inflammation, highlighting its protective role in the infarcted heart.https://doi.org/10.14814/phy2.70193fibrosisinflammationmyocardial infarctionoxidative stress
spellingShingle Katie C. Y. Lee
Allison L. Williams
Akitoshi Hara
Vedbar S. Khadka
Jeffrey Hayashi
Ralph V. Shohet
Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart
Physiological Reports
fibrosis
inflammation
myocardial infarction
oxidative stress
title Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart
title_full Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart
title_fullStr Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart
title_full_unstemmed Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart
title_short Loss of PKM2 dysregulates inflammatory signaling in the infarcted murine heart
title_sort loss of pkm2 dysregulates inflammatory signaling in the infarcted murine heart
topic fibrosis
inflammation
myocardial infarction
oxidative stress
url https://doi.org/10.14814/phy2.70193
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