Toronto General Hospital Research Institute, University Health Network, Toronto, ON, M5G 2C4, Canada.
Institute of Medical Science, University of Toronto, Toronto, ON, M5G 2M9, Canada.
Sci Rep. 2021 Feb 25;11(1):4723. doi: 10.1038/s41598-021-84063-6.
Inflammation is a key contributor to atherosclerosis with macrophages playing a pivotal role through the induction of oxidative stress and cytokine/chemokine secretion. DJ1, an anti-oxidant protein, has shown to paradoxically protect against chronic and acute inflammation. However, the role of DJ1 in atherosclerosis remains elusive. To assess the role of Dj1 in atherogenesis, we generated whole-body Dj1-deficient atherosclerosis-prone Apoe null mice (Dj1Apoe). After 21 weeks of atherogenic diet, Dj1 Apoemice were protected against atherosclerosis with significantly reduced plaque macrophage content. To assess whether haematopoietic or parenchymal Dj1 contributed to atheroprotection in Dj1-deficient mice, we performed bone-marrow (BM) transplantation and show that Dj1-deficient BM contributed to their attenuation in atherosclerosis. To assess cell-autonomous role of macrophage Dj1 in atheroprotection, BM-derived macrophages from Dj1-deficient mice and Dj1-silenced macrophages were assessed in response to oxidized low-density lipoprotein (oxLDL). In both cases, there was an enhanced anti-inflammatory response which may have contributed to atheroprotection in Dj1-deficient mice. There was also an increased trend of plasma DJ-1 levels from individuals with ischemic heart disease compared to those without. Our findings indicate an atheropromoting role of Dj1 and suggests that targeting Dj1 may provide a novel therapeutic avenue for atherosclerosis treatment or prevention.
炎症是动脉粥样硬化的一个关键因素,巨噬细胞通过诱导氧化应激和细胞因子/趋化因子的分泌在其中发挥关键作用。DJ1 是一种抗氧化蛋白,已被证明可以对抗慢性和急性炎症,但 DJ1 在动脉粥样硬化中的作用仍不清楚。为了评估 DJ1 在动脉粥样硬化形成中的作用,我们生成了全身性 DJ1 缺陷的动脉粥样硬化易感 Apoe 基因敲除小鼠(Dj1Apoe)。在用致动脉粥样硬化饮食喂养 21 周后,Dj1Apoe 小鼠可预防动脉粥样硬化,斑块内巨噬细胞含量明显减少。为了评估造血细胞或实质细胞 DJ1 是否有助于 DJ1 缺陷小鼠的动脉粥样硬化保护作用,我们进行了骨髓(BM)移植,并表明 DJ1 缺陷的 BM 有助于其在动脉粥样硬化中的衰减。为了评估巨噬细胞 DJ1 在动脉粥样硬化保护中的细胞自主作用,我们评估了来自 DJ1 缺陷小鼠和 DJ1 沉默巨噬细胞的 BM 来源巨噬细胞对氧化低密度脂蛋白(oxLDL)的反应。在这两种情况下,抗炎反应增强,这可能有助于 DJ1 缺陷小鼠的动脉粥样硬化保护。与没有缺血性心脏病的个体相比,患有缺血性心脏病的个体的血浆 DJ-1 水平也有增加的趋势。我们的研究结果表明 DJ1 具有促动脉粥样硬化作用,并表明靶向 DJ1 可能为动脉粥样硬化的治疗或预防提供新的治疗途径。