Morishita Yoshihiro, Kobayashi Koichi, Klyachko Ekaterina, Jujo Kentaro, Maeda Kengo, Losordo Douglas W, Murohara Toyoaki
Department of Cardiology, Nagoya University Graduate School of Medicine, Nagoya 466-8560, Japan.
Feinberg Cardiovascular Research Institute, Northwestern University School of Medicine, Chicago, IL 60611, USA.
Sci Rep. 2016 Feb 17;6:21705. doi: 10.1038/srep21705.
Acute myocardial infarction induces activation of the acute phase response and infiltration of leukocytes to the infarcted area. Moreover, myocardium that is remote from ischemic area also becomes inflamed. Inflammatory reaction clears dead cells and matrix debris, while prolongation or expansion of the inflammatory response results in dysfunction following myocardial infarction. Wnt glycolipoproteins are best characterized as regulators of embryonic development. Recently several reports suggest that they also contribute to the inflammatory response in adult animals. However, the effects of Wnt proteins on myocardial infarction have not been explored. Here we show that Wnt11 expression leads to significant improvements of survival and cardiac function by suppressing infiltration of multiple kinds of inflammatory cells in infarcted heart. Wnt11 protein suppresses gene expression of inflammatory cytokines through the modulation of NF-κB in vitro. These results reveal a novel function of Wnt11 in the regulation of inflammatory response and provide a rationale for the use of Wnt11 to manipulate human diseases that are mediated by inflammation.
急性心肌梗死会引发急性期反应的激活以及白细胞向梗死区域的浸润。此外,远离缺血区域的心肌也会发生炎症。炎症反应可清除死亡细胞和基质碎片,而炎症反应的延长或扩展会导致心肌梗死后的功能障碍。Wnt糖脂蛋白作为胚胎发育的调节因子最为人所熟知。最近有几份报告表明,它们也参与成年动物的炎症反应。然而,Wnt蛋白对心肌梗死的影响尚未得到研究。在这里,我们表明Wnt11的表达通过抑制梗死心脏中多种炎症细胞的浸润,显著改善了生存率和心脏功能。Wnt11蛋白在体外通过调节NF-κB抑制炎症细胞因子的基因表达。这些结果揭示了Wnt11在炎症反应调节中的新功能,并为使用Wnt11来治疗由炎症介导的人类疾病提供了理论依据。