From the Division of Molecular Medicine, Department of Medicine, Columbia University, New York (P.F., D.G.T., M.W., M.M.M., E.A., S.A., N.W., A.R.T.).
Department of Medicine, Division of Metabolism, Endocrinology and Nutrition, UW Medicine Diabetes Institute, University of Washington, Seattle (V.K., Y.H., J.W.H., K.E.B.).
Arterioscler Thromb Vasc Biol. 2019 Dec;39(12):e253-e272. doi: 10.1161/ATVBAHA.119.313253. Epub 2019 Oct 3.
HDL (high-density lipoprotein) infusion reduces atherosclerosis in animal models and is being evaluated as a treatment in humans. Studies have shown either anti- or proinflammatory effects of HDL in macrophages, and there is no consensus on the underlying mechanisms. Here, we interrogate the effects of HDL on inflammatory gene expression in macrophages. Approach and Results: We cultured bone marrow-derived macrophages, treated them with reconstituted HDL or HDL isolated from mice, and challenged them with lipopolysaccharide. Transcriptional profiling showed that HDL exerts a broad anti-inflammatory effect on lipopolysaccharide-induced genes and proinflammatory effect in a subset of genes enriched for chemokines. Cholesterol removal by POPC (1-palmitoyl-2-oleoyl-glycero-3-phosphocholine) liposomes or β-methylcyclodextrin mimicked both pro- and anti-inflammatory effects of HDL, whereas cholesterol loading by POPC/cholesterol-liposomes or acetylated LDL (low-density lipoprotein) before HDL attenuated these effects, indicating that these responses are mediated by cholesterol efflux. While early anti-inflammatory effects reflect reduced TLR (Toll-like receptor) 4 levels, late anti-inflammatory effects are due to reduced IFN (interferon) receptor signaling. Proinflammatory effects occur late and represent a modified endoplasmic reticulum stress response, mediated by IRE1a (inositol-requiring enzyme 1a)/ASK1 (apoptosis signal-regulating kinase 1)/p38 MAPK (p38 mitogen-activated protein kinase) signaling, that occurs under conditions of extreme cholesterol depletion. To investigate the effects of HDL on inflammatory gene expression in myeloid cells in atherosclerotic lesions, we injected reconstituted HDL into or mice fed a Western-type diet. Reconstituted HDL infusions produced anti-inflammatory effects in lesion macrophages without any evidence of proinflammatory effects.
Reconstituted HDL infusions in hypercholesterolemic atherosclerotic mice produced anti-inflammatory effects in lesion macrophages suggesting a beneficial therapeutic effect of HDL in vivo.
高密度脂蛋白(HDL)输注可减少动物模型中的动脉粥样硬化,并正在被评估作为人类的一种治疗方法。研究表明,HDL 在巨噬细胞中具有抗炎或促炎作用,但其潜在机制尚无定论。在这里,我们研究了 HDL 对巨噬细胞中炎症基因表达的影响。
我们培养了骨髓来源的巨噬细胞,用重组 HDL 或从 小鼠中分离的 HDL 处理它们,并用脂多糖对它们进行刺激。转录谱分析显示,HDL 对脂多糖诱导的基因具有广泛的抗炎作用,并对一组富含趋化因子的基因具有促炎作用。POPC(1-棕榈酰-2-油酰基-甘油-3-磷酸胆碱)脂质体去除胆固醇或β-甲基环糊精模拟了 HDL 的促炎和抗炎作用,而 POPC/胆固醇脂质体或乙酰化 LDL(低密度脂蛋白)预处理 HDL 则减弱了这些作用,表明这些反应是由胆固醇流出介导的。虽然早期的抗炎作用反映了 TLR(Toll 样受体)4 水平的降低,但晚期的抗炎作用是由于 IFN(干扰素)受体信号的降低。促炎作用发生较晚,代表一种经过修饰的内质网应激反应,由 IRE1a(肌醇需要酶 1a)/ASK1(凋亡信号调节激酶 1)/p38 MAPK(p38 丝裂原活化蛋白激酶)信号介导,发生在极端胆固醇耗竭的情况下。为了研究 HDL 对动脉粥样硬化病变中髓样细胞炎症基因表达的影响,我们将重组 HDL 注入喂食西式饮食的 或 小鼠体内。HDL 再注射在动脉粥样硬化病变的巨噬细胞中产生了抗炎作用,而没有任何促炎作用的证据。
在高胆固醇血症的动脉粥样硬化小鼠中,HDL 再注射产生了病变巨噬细胞的抗炎作用,这表明 HDL 在体内具有有益的治疗作用。