基质金属蛋白酶
炎症
膜联蛋白A1
心肌梗塞
伤口愈合
弹性蛋白酶
脂毒素
医学
基质金属蛋白酶抑制剂
巨噬细胞
化学
细胞生物学
免疫学
膜联蛋白
生物
内科学
生物化学
流式细胞术
酶
体外
作者
Alan J. Mouton,O. J. Gonzalez,A Kaminski,Edwin T. Moore,Merry L. Lindsey
标识
DOI:10.1016/j.phrs.2018.10.026
摘要
Following myocardial infarction (MI), timely resolution of inflammation promotes wound healing and scar formation while limiting excessive tissue damage. Resolution promoting factors (RPFs) are agents that blunt leukocyte trafficking and inflammation, promote necrotic and apoptotic cell clearance, and stimulate scar formation. Previously identified RPFs include mediators derived from lipids (resolvins, lipoxins, protectins, and maresins), proteins (glucocorticoids, annexin A1, galectin 1, and melanocortins), or gases (CO, H2S, and NO). Matrix metalloproteinase-12 (MMP-12; macrophage elastase) has shown promising RPF qualities in a variety of disease states. We review here the evidence that MMP-12 may serve as a novel RPF with potential therapeutic efficacy in the setting of MI.
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