Wan Feng, Letavernier Emmanuel, Le Saux Claude Jourdan, Houssaini Amal, Abid Shariq, Czibik Gabor, Sawaki Daigo, Marcos Elisabeth, Dubois-Rande Jean-Luc, Baud Laurent, Adnot Serge, Derumeaux Geneviève, Gellen Barnabas
Institut National de la Santé et de la Recherche Médicale U955, Université Paris-Est Creteil, Créteil, France;
Department of Physiology, Assistance Publique-Hôpitaux de Paris (AP-HP), Tenon Hospital, Paris, France; Inflammation-Immunopathology-Biotherapy Department (DHU i2B), F-75020, Sorbonne Universités, Université Pierre et Marie Curie, Université Paris 06, Unités Mixtes de Recherche Scientifique 1155, Paris, France; and.
Am J Physiol Heart Circ Physiol. 2015 Dec 1;309(11):H1883-93. doi: 10.1152/ajpheart.00594.2015. Epub 2015 Oct 9.
The activation of the calpain system is involved in the repair process following myocardial infarction (MI). However, the impact of the inhibition of calpain by calpastatin, its natural inhibitor, on scar healing and left ventricular (LV) remodeling is elusive. Male mice ubiquitously overexpressing calpastatin (TG) and wild-type (WT) controls were subjected to an anterior coronary artery ligation. Mortality at 6 wk was higher in TG mice (24% in WT vs. 44% in TG, P < 0.05) driven by a significantly higher incidence of cardiac rupture during the first week post-MI, despite comparable infarct size and LV dysfunction and dilatation. Calpain activation post-MI was blunted in TG myocardium. In TG mice, inflammatory cell infiltration and activation were reduced in the infarct zone (IZ), particularly affecting M2 macrophages and CD4(+) T cells, which are crucial for scar healing. To elucidate the role of calpastatin overexpression in macrophages, we stimulated peritoneal macrophages obtained from TG and WT mice in vitro with IL-4, yielding an abrogated M2 polarization in TG but not in WT cells. Lymphopenic Rag1(-/-) mice receiving TG splenocytes before MI demonstrated decreased T-cell recruitment and M2 macrophage activation in the IZ day 5 after MI compared with those receiving WT splenocytes. Calpastatin overexpression prevented the activation of the calpain system after MI. It also impaired scar healing, promoted LV rupture, and increased mortality. Defective scar formation was associated with blunted CD4(+) T-cell and M2-macrophage recruitment.
钙蛋白酶系统的激活参与心肌梗死(MI)后的修复过程。然而,其天然抑制剂钙蛋白酶抑制蛋白对瘢痕愈合和左心室(LV)重塑的影响尚不清楚。对普遍过表达钙蛋白酶抑制蛋白的雄性小鼠(TG)和野生型(WT)对照进行冠状动脉前降支结扎。尽管梗死面积、LV功能障碍和扩张程度相当,但TG小鼠在6周时的死亡率更高(WT为24%,TG为44%,P<0.05),这是由于MI后第一周心脏破裂的发生率显著更高。MI后TG心肌中的钙蛋白酶激活受到抑制。在TG小鼠中,梗死区(IZ)的炎症细胞浸润和激活减少,尤其影响对瘢痕愈合至关重要的M2巨噬细胞和CD4(+)T细胞。为了阐明钙蛋白酶抑制蛋白过表达在巨噬细胞中的作用,我们用IL-4体外刺激从TG和WT小鼠获得的腹腔巨噬细胞,结果发现TG细胞中M2极化被消除,而WT细胞中未被消除。在MI前接受TG脾细胞的淋巴细胞减少的Rag1(-/-)小鼠,与接受WT脾细胞的小鼠相比,在MI后第5天IZ中的T细胞募集和M2巨噬细胞激活减少。钙蛋白酶抑制蛋白过表达可防止MI后钙蛋白酶系统的激活。它还损害瘢痕愈合,促进LV破裂,并增加死亡率。瘢痕形成缺陷与CD4(+)T细胞和M2巨噬细胞募集减少有关。