共 19 条
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
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页码:871 / 881
页数:11
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