The time-of-day of myocardial infarction onset affects healing through oscillations in cardiac neutrophil recruitment

被引:119
作者
Schloss, Maximilian J. [1 ]
Horckmans, Michael [1 ]
Nitz, Katrin [1 ,2 ]
Duchene, Johan [1 ]
Drechsler, Maik [1 ,3 ,4 ]
Bidzhekov, Kiril [1 ]
Scheiermann, Christoph [5 ]
Weber, Christian [1 ,3 ,6 ]
Soehnlein, Oliver [1 ,3 ,4 ]
Steffens, Sabine [1 ,3 ]
机构
[1] Ludwig Maximilians Univ LMU Munich, Inst Cardiovasc Prevent IPEK, Munich, Germany
[2] Helmholtz Assoc, Max Delbrueck Ctr Mol Med, Berlin, Germany
[3] Partner Site Munich Heart Alliance, German Ctr Cardiovasc Res DZHK, Munich, Germany
[4] AMC, Dept Pathol, Amsterdam, Netherlands
[5] Ludwig Maximilians Univ LMU Munich, Walter Brendel Ctr Expt Med, Munich, Germany
[6] Maastricht Univ, Dept Biochem, Cardiovasc Res Inst Maastricht CARIM, Maastricht, Netherlands
基金
欧洲研究理事会;
关键词
circadian rhythm; fibrosis; myocardial infarction healing; neutrophils; progenitors; CIRCADIAN VARIATIONS; INFLAMMATION; SIZE; ISCHEMIA/REPERFUSION; MACROPHAGE; MONOCYTES; DEPLETION; SYSTEM; INJURY; REPAIR;
D O I
10.15252/emmm.201506083
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Myocardial infarction (MI) is the leading cause of death in Western countries. Epidemiological studies show acute MI to be more prevalent in the morning and to be associated with a poorer outcome in terms of mortality and recovery. The mechanisms behind this association are not fully understood. Here, we report that circadian oscillations of neutrophil recruitment to the heart determine infarct size, healing, and cardiac function after MI. Preferential cardiac neutrophil recruitment during the active phase (Zeitgeber time, ZT13) was paralleled by enhanced myeloid progenitor production, increased circulating numbers of CXCR2(hi) neutrophils as well as upregulated cardiac adhesion molecule and chemokine expression. MI at ZT13 resulted in significantly higher cardiac neutrophil infiltration compared to ZT5, which was inhibited by CXCR2 antagonism or neutrophil-specific CXCR2 knockout. Limiting exaggerated neutrophilic inflammation at this time point significantly reduced the infarct size and improved cardiac function.
引用
收藏
页码:937 / 948
页数:12
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