Monocytes/macrophages prevent healing defects and left ventricular thrombus formation after myocardial infarction

被引:161
作者
Frantz, Stefan [1 ,3 ]
Hofmann, Ulrich [1 ,3 ]
Fraccarollo, Daniela [5 ]
Schaefer, Andreas [5 ]
Kranepuhl, Stefanie [1 ]
Hagedorn, Ina [2 ,3 ]
Nieswandt, Bernhard [2 ,3 ]
Nahrendorf, Matthias [6 ]
Wagner, Helga [1 ,3 ]
Bayer, Barbara [1 ,3 ]
Pachel, Christina [1 ,3 ]
Schoen, Michael P. [7 ]
Kneitz, Susanne [4 ]
Bobinger, Tobias [1 ]
Weidemann, Frank [1 ,3 ]
Ertl, Georg [1 ,3 ]
Bauersachs, Johann [5 ]
机构
[1] Univ Hosp Wurzburg, Dept Internal Med 1, Rudolf Virchow Ctr, Wurzburg, Germany
[2] Univ Hosp Wurzburg, Rudolf Virchow Ctr, Dept Vasc Med, Wurzburg, Germany
[3] Univ Wurzburg, Comprehens Heart Failure Ctr, Microarray Core Facil, D-97080 Wurzburg, Germany
[4] Univ Wurzburg, Interdisciplinary Ctr Clin Res, Microarray Core Facil, D-97080 Wurzburg, Germany
[5] Hannover Med Sch, Dept Cardiol & Angiol, D-30623 Hannover, Germany
[6] Massachusetts Gen Hosp, Ctr Syst Biol, Boston, MA 02114 USA
[7] Univ Gottingen, Dept Dermatol Venereol & Allergol, D-37073 Gottingen, Germany
关键词
extracellular matrix; ischemia; inflammation; MONOCYTE SUBSETS; MICE; ACTIVATION; EXPRESSION; IMPACT;
D O I
10.1096/fj.12-214049
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
Myocardial infarction (MI) leads to rapid necrosis of cardiac myocytes. To achieve tissue integrity and function, inflammatory cells are activated, including monocytes/macrophages. However, the effect of monocyte/macrophage recruitment after MI remains poorly defined. After experimental MI, monocytes and macrophages were depleted through serial injections of clodronate-containing liposomes. Monocyte/macrophage infiltration was reduced in the myocardium after MI by active treatment. Mortality was increased due to thromboembolic events in monocyte-and macrophage-depleted animals (92 vs. 33%; P<0.01). Left ventricular thrombi were detectable as early as 24 h after MI; this was reproduced in a genetic model of monocyte/macrophage ablation. A general prothrombotic state, increased infarct expansion, and deficient neovascularization were not observed. Severely compromised extracellular matrix remodeling (collagen I, placebo liposome vs. clodronate liposome, 2.4 +/- 0.2 vs. 0.8 +/- 0.2 arbitrary units; P<0.001) and locally lost integrity of the endocardium after MI are potential mechanisms. Patients with a left ventricular thrombus had a relative decrease of CD14(+) CD16(+) monocyte/macrophage subsets in the peripheral blood after MI (no thrombus vs. thrombus, 14.2 +/- 0.9 vs. 7.80 +/- 0.4%; P<0.05). In summary, monocytes/macrophages are of central importance for healing after MI. Impaired monocyte/macrophage function appears to be an unrecognized new pathophysiological mechanism for left ventricular thrombus development after MI.-Frantz, S., Hofmann, U., Fraccarollo, D., Schafer, A., Kranepuhl, S., Hagedorn, I., Nieswandt, B., Nahrendorf, M., Wagner, H., Bayer, B., Pachel, C., Schon, M.P., Kneitz, S., Bobinger, T., Weidemann, F., Ertl, G., Bauersachs, J. Monocytes/macrophages prevent healing defects and left ventricular thrombus formation after myocardial infarction. FASEB J. 27, 871-881 (2013). www.fasebj.org
引用
收藏
页码:871 / 881
页数:11
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