Activator protein-1 and caspase 8 mediate p38α MAPK-dependent cardiomyocyte apoptosis induced by palmitic acid

Charles C. Oh, John Lee, Karen D’Souza, Weiyang Zhang, Raymond Q. Migrino, Kent Thornburg, Peter Reaven

    Research output: Contribution to journalArticle

    Abstract

    Lipoapoptosis of cardiomyocytes may underlie diabetic cardiomyopathy. Numerous forms of cardiomyopathies share a common end-pathway in which apoptotic loss of cardiomyocytes is mediated by p38α mitogen activated protein kinase (MAPK). Although we have previously shown that palmitic acid (PA), a saturated fatty acid (SFA) elevated in plasma of type 2 diabetes mellitus and morbid obesity, induces apoptosis in cardiomyocytes via p38α MAPK-dependent signaling, the downstream cascade events that cause cell death remain unknown. The objective of this study was to investigate mechanisms involved in palmitic acid-induced cardiomyocyte apoptosis. Human adult ventricular cardiomyocyte line (AC16 cells) exposed to high physiological levels of PA for 16 h showed enhanced transcription and phosphorylation of c-fos and c-jun subunits of AP-1 and transcription of caspase 8. When AC16 cells were transfected with small interfering RNA specific against p38α MAPK (si-p38α) for 24 or 48 h, the amplified phosphorylation of c-fos was dose-dependently attenuated, and procaspase 8 was dose-dependently reduced. With translational knockdown of c-fos, PA-induced apoptosis was diminished. Inhibition of caspase 8 for 24 h reduced apoptosis in PA-treated cardiomyocytes. These findings provide evidence for induction of apoptosis in cardiomyocytes exposed to high SFA by a novel pathway requiring activation of c-fos/AP-1 and caspase 8. These results demonstrate how elevated plasma SFA may lead to continual and cumulative loss of cardiomyocytes and potentially contribute to the development of diabetic cardiomyopathy.

    Original languageEnglish (US)
    JournalApoptosis
    DOIs
    StatePublished - Jan 1 2019

    Fingerprint

    Palmitic Acid
    Caspase 8
    Transcription Factor AP-1
    p38 Mitogen-Activated Protein Kinases
    Cardiac Myocytes
    Apoptosis
    Phosphorylation
    Fatty Acids
    Transcription
    Diabetic Cardiomyopathies
    Plasmas
    Cell death
    Medical problems
    Small Interfering RNA
    Chemical activation
    Morbid Obesity
    Cardiomyopathies
    Type 2 Diabetes Mellitus
    Cause of Death
    Cell Death

    Keywords

    • AP-1
    • Apoptosis
    • Caspase 8
    • Diabetic cardiomyopathy
    • P38α

    ASJC Scopus subject areas

    • Pharmacology
    • Pharmaceutical Science
    • Clinical Biochemistry
    • Cell Biology
    • Biochemistry, medical
    • Cancer Research

    Cite this

    Activator protein-1 and caspase 8 mediate p38α MAPK-dependent cardiomyocyte apoptosis induced by palmitic acid. / Oh, Charles C.; Lee, John; D’Souza, Karen; Zhang, Weiyang; Migrino, Raymond Q.; Thornburg, Kent; Reaven, Peter.

    In: Apoptosis, 01.01.2019.

    Research output: Contribution to journalArticle

    Oh, Charles C. ; Lee, John ; D’Souza, Karen ; Zhang, Weiyang ; Migrino, Raymond Q. ; Thornburg, Kent ; Reaven, Peter. / Activator protein-1 and caspase 8 mediate p38α MAPK-dependent cardiomyocyte apoptosis induced by palmitic acid. In: Apoptosis. 2019.
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