• Jae W Lee, Michael Koeppen, Seong-Wook Seo, Jessica L Bowser, Xiaoyi Yuan, Jiwen Li, Maria Sibilia, Amrut V Ambardekar, Xu Zhang, Tobias Eckle, Seung-Hee Yoo, and Holger K Eltzschig.
• From the Department of Anesthesiology, The University of Texas Health Science Center at Houston, McGovern Medical School, Houston, Texas (J.W.L., J.L.B., X.Y., J.L., H.K.E.) Department of Anesthesiology and Intensive Care Medicine, Tübingen University Hospital, Eberhard-Karls University Tübingen, Tübingen, Germany (M.K.) Department of Anesthesiology, University of New Mexico School of Medicine, Albuquerque, New Mexico (S.-W.S.) Department of Cardiac Surgery, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou, China (J.L.) Institute for Cancer Research, Department of Medicine, Medical University of Vienna, Vienna, Austria (M.S.) Division of Cardiology, Department of Medicine, University of Colorado School of Medicine, Aurora, Colorado (A.V.A.) Center for Clinical and Translational Sciences, The University of Texas Health Science Center at Houston, Houston, Texas (X.Z.) Department of Anesthesiology, University of Colorado School of Medicine, Aurora, Colorado (T.E.) Department of Biochemistry and Molecular Biology, The University of Texas Health Science Center at Houston, McGovern Medical School, Houston, Texas (S.-H.Y.).
• Anesthesiology. 2020 Apr 1; 132 (4): 763-780.

BackgroundDuring myocardial ischemia, hypoxia-inducible factors are stabilized and provide protection from ischemia and reperfusion injury. Recent studies show that myocyte-specific hypoxia-inducible factor 2A promotes myocardial ischemia tolerance through induction of epidermal growth factor, amphiregulin. Here, the authors hypothesized that hypoxia-inducible factor 2A may enhance epidermal growth factor receptor 1 (ERBB1) expression in the myocardium that could interface between growth factors and its effect on providing tolerance to ischemia and reperfusion injury.MethodsHuman myocardial tissues were obtained from ischemic heart disease patients and normal control patients to compare ERBB1 expression. Myocyte-specific Hif2a or ErbB1 knockout mice were generated to observe the effect of Hif2a knockdown in regulating ERBB1 expression and to examine the role of ERBB1 during myocardial ischemia and reperfusion injury.ResultsInitial studies of myocardial tissues from patients with ischemic heart disease showed increased ERBB1 protein (1.12 ± 0.24 vs. 13.01 ± 2.20, P < 0.001). In contrast, ERBB1 transcript was unchanged. Studies using short hairpin RNA repression of Hif2A or Hif2a Myosin Cre+ mice directly implicated hypoxia-inducible factor 2A in ERBB1 protein induction during hypoxia or after myocardial ischemia, respectively. Repression of RNA-binding protein 4 abolished hypoxia-inducible factor 2A-dependent induction of ERBB1 protein. Moreover, ErbB1 Myosin Cre+ mice experienced larger infarct sizes (22.46 ± 4.06 vs. 46.14 ± 1.81, P < 0.001) and could not be rescued via amphiregulin treatment.ConclusionsThese findings suggest that hypoxia-inducible factor 2A promotes transcription-independent induction of ERBB1 protein and implicates epidermal growth factor signaling in protection from myocardial ischemia and reperfusion injury.

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