Liang Chien-Ping, Han Seongah, Senokuchi Takafumi, Tall Alan R
Division of Molecular Medicine, Department of Medicine, Columbia University, New York, NY 10032, USA.
Circ Res. 2007 Jun 8;100(11):1546-55. doi: 10.1161/CIRCRESAHA.107.152165.
The macrophage has emerged as an important player in the pathogenesis of both atherosclerosis and insulin resistance. Cross-talk between inflammatory macrophages and adipocytes may be involved in insulin resistance in peripheral tissues. Defective insulin signaling in cells of the arterial wall including macrophages may promote the development of atherosclerosis. Insulin resistant macrophages are more susceptible to endoplasmic reticulum stress and apoptosis in response to various stimuli such as nutrient deprivation, free cholesterol loading, and oxidized LDL. Increased apoptosis of insulin resistant macrophages and impaired phagocytic clearance of apoptotic cells by insulin resistant macrophages in atherosclerotic lesions may lead to enhanced postapoptotic necrosis, larger lipid-rich cores, increased inflammation, and more complex vulnerable plaques.
巨噬细胞已成为动脉粥样硬化和胰岛素抵抗发病机制中的重要参与者。炎症性巨噬细胞与脂肪细胞之间的相互作用可能与外周组织的胰岛素抵抗有关。动脉壁细胞(包括巨噬细胞)中胰岛素信号传导缺陷可能会促进动脉粥样硬化的发展。胰岛素抵抗的巨噬细胞对内质网应激更敏感,并且在受到各种刺激(如营养剥夺、游离胆固醇负荷和氧化低密度脂蛋白)时更易发生凋亡。动脉粥样硬化病变中胰岛素抵抗巨噬细胞的凋亡增加以及胰岛素抵抗巨噬细胞对凋亡细胞的吞噬清除受损,可能导致凋亡后坏死增强、富含脂质的核心更大、炎症增加以及更复杂的易损斑块。