Adora2b-elicited Per2 stabilization promotes a HIF-dependent metabolic switch crucial for myocardial adaptation to ischemia

被引:266
作者
Eckle, Tobias [1 ]
Hartmann, Katherine [1 ]
Bonney, Stephanie [1 ]
Reithel, Susan [1 ]
Mittelbronn, Michel [2 ]
Walker, Lori A. [3 ]
Lowes, Brian D. [3 ]
Han, Jun [4 ]
Borchers, Christoph H. [4 ]
Buttrick, Peter M. [3 ]
Kominsky, Douglas J. [1 ]
Colgan, Sean P. [5 ]
Eltzschig, Holger K. [1 ]
机构
[1] Univ Colorado Denver, Dept Anesthesiol, Mucosal Inflammat Program, Aurora, CO USA
[2] Goethe Univ Frankfurt, Edinger Inst, Inst Neurol, Frankfurt, Germany
[3] Univ Colorado Denver, Div Cardiol, Dept Med, Aurora, CO USA
[4] Univ Victoria, Dept Biochem & Microbiol, Genome BC Prote Ctr, Victoria, BC, Canada
[5] Univ Colorado Denver, Dept Med, Mucosal Inflammat Program, Aurora, CO USA
关键词
CIRCADIAN CLOCK; GLUCOSE-METABOLISM; TISSUE-DAMAGE; INFARCT SIZE; MOUSE MODEL; ADENOSINE; HYPOXIA; REPERFUSION; MECHANISMS; EXPRESSION;
D O I
10.1038/nm.2728
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Adenosine signaling has been implicated in cardiac adaptation to limited oxygen availability. In a wide search for adenosine receptor A2b (Adora2b)-elicited cardioadaptive responses, we identified the circadian rhythm protein period 2 (Per2) as an Adora2b target. Adora2b signaling led to Per2 stabilization during myocardial ischemia, and in this setting, Per2(-/-) mice had larger infarct sizes compared to wild-type mice and loss of the cardioprotection conferred by ischemic preconditioning. Metabolic studies uncovered a limited ability of ischemic hearts in Per2(-/-) mice to use carbohydrates for oxygen-efficient glycolysis. This impairment was caused by a failure to stabilize hypoxia-inducible factor-1 alpha (Hif-1 alpha). Moreover, stabilization of Per2 in the heart by exposing mice to intense light resulted in the transcriptional induction of glycolytic enzymes and Per2-dependent cardioprotection from ischemia. Together, these studies identify adenosine-elicited stabilization of Per2 in the control of HIF-dependent cardiac metabolism and ischemia tolerance and implicate Per2 stabilization as a potential new strategy for treating myocardial ischemia.
引用
收藏
页码:774 / U173
页数:11
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