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    Mdm2 regulates cardiac contractility by inhibiting GRK2-mediated desensitization of beta-adrenergic receptor signaling

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    Authors
    Jean-Charles, Pierre-Yves
    Yu, Samuel Mon-Wei
    Abraham, Dennis
    Kommaddi, Reddy Peera.
    Mao, Lan
    Strachan, Ryan T.
    Zhang, Zhu-Shan
    Bowles, Dawn E.
    Brian, Leigh
    Stiber, Jonathan A.
    Jones, Stephen N.
    Koch, Walter J.
    Rockman, Howard A.
    Shenoy, Sudha K.
    Show allShow less
    UMass Chan Affiliations
    Stephen Jones Lab
    Department of Cell and Developmental Biology
    Document Type
    Journal Article
    Publication Date
    2017-09-07
    Keywords
    Cardiology
    Oncology
    Heart failure
    Ubiquitin-proteosome system
    Cardiology
    Cell Biology
    Developmental Biology
    Oncology
    
    Metadata
    Show full item record
    Link to Full Text
    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5621915/
    Abstract
    The oncoprotein Mdm2 is a RING domain-containing E3 ubiquitin ligase that ubiquitinates G protein-coupled receptor kinase 2 (GRK2) and beta-arrestin2, thereby regulating beta-adrenergic receptor (betaAR) signaling and endocytosis. Previous studies showed that cardiac Mdm2 expression is critical for controlling p53-dependent apoptosis during early embryonic development, but the role of Mdm2 in the developed adult heart is unknown. We aimed to identify if Mdm2 affects betaAR signaling and cardiac function in adult mice. Using Mdm2/p53-KO mice, which survive for 9-12 months, we identified a critical and potentially novel role for Mdm2 in the adult mouse heart through its regulation of cardiac beta1AR signaling. While baseline cardiac function was mostly similar in both Mdm2/p53-KO and wild-type (WT) mice, isoproterenol-induced cardiac contractility in Mdm2/p53-KO was significantly blunted compared with WT mice. Isoproterenol increased cAMP in left ventricles of WT but not of Mdm2/p53-KO mice. Additionally, while basal and forskolin-induced calcium handling in isolated Mdm2/p53-KO and WT cardiomyocytes were equivalent, isoproterenol-induced calcium handling in Mdm2/p53-KO was impaired. Mdm2/p53-KO hearts expressed 2-fold more GRK2 than WT. GRK2 polyubiquitination via lysine-48 linkages was significantly reduced in Mdm2/p53-KO hearts. Tamoxifen-inducible cardiomyocyte-specific deletion of Mdm2 in adult mice also led to a significant increase in GRK2, and resulted in severely impaired cardiac function, high mortality, and no detectable betaAR responsiveness. Gene delivery of either Mdm2 or GRK2-CT in vivo using adeno-associated virus 9 (AAV9) effectively rescued beta1AR-induced cardiac contractility in Mdm2/p53-KO. These findings reveal a critical p53-independent physiological role of Mdm2 in adult hearts, namely, regulation of GRK2-mediated desensitization of betaAR signaling.
    Source

    JCI Insight. 2017 Sep 7;2(17). pii: 95998. doi: 10.1172/jci.insight.95998. Link to article on publisher's site

    DOI
    10.1172/jci.insight.95998
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/40458
    PubMed ID
    28878120
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    Link to Article in PubMed

    ae974a485f413a2113503eed53cd6c53
    10.1172/jci.insight.95998
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