Hamczyk Magda R, Villa-Bellosta Ricardo, Andrés Vicente
Laboratory of Molecular and Genetic Cardiovascular Pathophysiology, Vascular Biology Program, Centro Nacional de Investigaciones Cardiovasculares Carlos III (CNIC), Madrid, Spain.
Methods Mol Biol. 2015;1339:235-46. doi: 10.1007/978-1-4939-2929-0_16.
The key roles of macrophages in atherosclerosis include the phagocytosis of apoptotic and necrotic cells and cell debris, whose accumulation in atherosclerotic lesions exacerbates inflammation and promotes plaque vulnerability. Evidence is accumulating that macrophage phagocytic functions peak at the early stages of atherosclerosis and that the reduced phagocytosis at the late stages of disease leads to the generation of necrotic cores and a defective resolution of inflammation, which in turn promotes plaque rupture, thrombus formation, and life-threatening acute ischemic events (myocardial infarction and stroke). The impaired resolution of inflammation in advanced lesions featuring loss of macrophage phagocytic activity may be in part due to an imbalance between M1 and M2 subsets of polarized macrophages. A better understanding of the mechanisms that regulate macrophage phagocytic activity in the context of atherosclerosis may therefore help identify novel therapeutic targets. This chapter presents a protocol for establishing primary mouse macrophage cultures, a method for polarizing macrophages to the M1 and M2 states, and a method for the in vitro study of macrophage phagocytosis of IgG-opsonized or IgM/complement component 3-opsonized erythrocytes.
巨噬细胞在动脉粥样硬化中的关键作用包括吞噬凋亡细胞、坏死细胞和细胞碎片,这些物质在动脉粥样硬化病变中的积累会加剧炎症并促进斑块易损性。越来越多的证据表明,巨噬细胞的吞噬功能在动脉粥样硬化早期达到峰值,而疾病后期吞噬作用的降低会导致坏死核心的形成以及炎症消退缺陷,进而促进斑块破裂、血栓形成和危及生命的急性缺血事件(心肌梗死和中风)。在以巨噬细胞吞噬活性丧失为特征的晚期病变中,炎症消退受损可能部分归因于极化巨噬细胞的M1和M2亚群之间的失衡。因此,更好地了解在动脉粥样硬化背景下调节巨噬细胞吞噬活性的机制可能有助于确定新的治疗靶点。本章介绍了建立原代小鼠巨噬细胞培养物的方案、将巨噬细胞极化为M1和M2状态的方法,以及体外研究巨噬细胞对IgG调理或IgM/补体成分3调理红细胞吞噬作用 的方法。