Institute of Experimental Medicine, St. Petersburg, 197376, Russia.
St. Petersburg State University, St. Petersburg, 199034, Russia.
Biochemistry (Mosc). 2021 Oct;86(10):1201-1213. doi: 10.1134/S0006297921100047.
Apolipoprotein A-I (ApoA-I) is a key component of reverse cholesterol transport in humans. In the previous studies, we demonstrated expression of the apoA-I gene in human monocytes and macrophages; however, little is known on the regulation of the apoA-I expression in macrophages during the uptake of modified low-density lipoprotein (LDL), which is one of the key processes in the early stages of atherogenesis leading to formation of foam cells. Here, we demonstrate a complex nature of the apoA-I regulation in human macrophages during the uptake of oxidized LDL (oxLDL). Incubation of macrophages with oxLDL induced expression of the apoA-I gene within the first 24 hours, but suppressed it after 48 h. Both effects depended on the interaction of oxLDL with the TLR4 receptor, rather than on the oxLDL uptake by the macrophages. The oxLDL-mediated downregulation of the apoA-I gene depended on the ERK1/2 and JNK cascades, as well as on the NF-κB cascade.
载脂蛋白 A-I(ApoA-I)是人类胆固醇逆向转运的关键组成部分。在之前的研究中,我们证明了载脂蛋白 A-I 基因在人类单核细胞和巨噬细胞中的表达;然而,对于在摄取修饰的低密度脂蛋白(LDL)过程中,即导致泡沫细胞形成的动脉粥样硬化早期阶段的关键过程之一,巨噬细胞中载脂蛋白 A-I 的表达调控知之甚少。在这里,我们在人类巨噬细胞摄取氧化 LDL(oxLDL)过程中证明了载脂蛋白 A-I 调控的复杂性。巨噬细胞与 oxLDL 孵育会在最初的 24 小时内诱导载脂蛋白 A-I 基因的表达,但在 48 小时后会抑制其表达。这两种作用都依赖于 oxLDL 与 TLR4 受体的相互作用,而不是巨噬细胞对 oxLDL 的摄取。oxLDL 介导的载脂蛋白 A-I 基因下调依赖于 ERK1/2 和 JNK 级联,以及 NF-κB 级联。