Department of Cardiovascular Medicine, Hokkaido University Graduate School of Medicine, Kita-15 Nishi-7, Kita-ku, Sapporo 060-8638, Japan.
Department of Cardiovascular Medicine, National Defense Medical College, Namiki 3-2, Tokorozawa 359-0042, Japan.
Int J Mol Sci. 2021 Nov 18;22(22):12451. doi: 10.3390/ijms222212451.
The infiltration and activation of macrophages as well as lymphocytes within atherosclerotic lesion contribute to the pathogenesis of plaque rupture. We have demonstrated that invariant natural killer T (iNKT) cells, a unique subset of T lymphocytes that recognize glycolipid antigens, play a crucial role in atherogenesis. However, it remained unclear whether iNKT cells are also involved in plaque instability. Apolipoprotein E (apoE) knockout mice were fed a standard diet (SD) or a high-fat diet (HFD) for 8 weeks. Moreover, the SD- and the HFD-fed mice were divided into two groups according to the intraperitoneal injection of α-galactosylceramide (αGC) that specifically activates iNKT cells or phosphate-buffered saline alone (PBS). ApoE/Jα18 double knockout mice, which lack iNKT cells, were also fed an SD or HFD. Plaque instability was assessed at the brachiocephalic artery by the histological analysis. In the HFD group, αGC significantly enhanced iNKT cell infiltration and exacerbated atherosclerotic plaque instability, whereas the depletion of iNKT cells attenuated plaque instability compared to PBS-treated mice. Real-time PCR analyses in the aortic tissues showed that αGC administration significantly increased expressional levels of inflammatory genes such as IFN-γ and MMP-2, while the depletion of iNKT cells attenuated these expression levels compared to those in the PBS-treated mice. Our findings suggested that iNKT cells are involved in the exacerbation of plaque instability via the activation of inflammatory cells and upregulation of MMP-2 in the vascular tissues.
巨噬细胞和淋巴细胞浸润并激活在动脉粥样硬化病变的发病机制中起作用。我们已经证明,固有自然杀伤 T(iNKT)细胞,一种识别糖脂抗原的独特 T 淋巴细胞亚群,在动脉粥样硬化形成中发挥关键作用。然而,iNKT 细胞是否也参与斑块不稳定仍然不清楚。载脂蛋白 E(apoE)敲除小鼠喂食标准饮食(SD)或高脂肪饮食(HFD)8 周。此外,根据腹腔内注射特异性激活 iNKT 细胞的α-半乳糖神经酰胺(αGC)或单独磷酸盐缓冲盐水(PBS),将 SD 和 HFD 喂养的小鼠分为两组。缺乏 iNKT 细胞的 apoE/Jα18 双敲除小鼠也喂食 SD 或 HFD。通过肱动脉的组织学分析评估斑块不稳定性。在 HFD 组,αGC 显著增强 iNKT 细胞浸润并加剧动脉粥样硬化斑块不稳定,而与 PBS 处理的小鼠相比,iNKT 细胞耗竭则减轻斑块不稳定。主动脉组织的实时 PCR 分析显示,αGC 给药显著增加了炎症基因如 IFN-γ和 MMP-2 的表达水平,而与 PBS 处理的小鼠相比,iNKT 细胞耗竭则降低了这些表达水平。我们的研究结果表明,iNKT 细胞通过激活血管组织中的炎症细胞和上调 MMP-2 参与了斑块不稳定的加剧。