Cardiovascular Center/Division of Cardiology, Beijing Friendship Hospital, Capital Medical University, No. 95 Yong'an Road, Beijing City 100053, China.
Department of Cardiology, The First Affiliated Hospital of Dalian Medical University, Dalian City 116011, China.
Mediators Inflamm. 2019 May 6;2019:8709583. doi: 10.1155/2019/8709583. eCollection 2019.
Circulating monocytes play a critical role in the pathogenesis of atherosclerosis. Monocyte homing to sites of atherosclerosis is primarily initiated by selectin. Thus, blockade of the interaction of selectins and their ligands holds a significant role in monocyte homing which might be a potential approach to treat atherosclerosis. Here, we investigated the efficacy of a novel peptide analogue of selectin ligands IELLQAR in atherosclerosis.
In this study, we firstly measured the effect of the IELLQAR selectin-binding peptide on the inhibition of binding of selectins to monocytes by flow cytometry, which exhibited a dose-dependent inhibitory effect on the binding of the P-, E-, and L-selectins to monocytes, especially the inhibition of P-selectin binding to human peripheral blood monocytes (PBMCs) (half maximal inhibitory concentration (IC5 M)) and THP-1 cells (IC10 M). Furthermore, IELLQAR inhibited P-selectin-induced activation of CD11b on the surface of monocytes and decreased adhesion of monocytes to the endothelium mice with or without IELLQAR (1 or 3 mg/kg) fed a Western-type diet (WTD) or which had disturbed blood flow-induced shear stress underwent partial left carotid artery ligation (PLCA) to induce atherosclerosis. In the WTD- and PLCA-induced atherosclerosis models, atherosclerotic plaque formation and monocyte/macrophage infiltration of the arterial wall both decreased in  mice treated with the IELLQAR peptide. Our results also revealed that IELLQAR inhibited the differentiation of monocytes into macrophages through P-selectin-dependent activation of the nuclear factor- (NF-) B and mammalian target of rapamycin (mTOR) pathways.
Collectively, our results demonstrated that IELLQAR, a peptide analogue of selectin ligands, inhibited selectin binding to monocytes, which led to subsequent attenuation of atherosclerosis via inhibition of monocyte activation. Hence, use of the IELLQAR peptide provides a new approach and represents a promising candidate for the treatment of atherosclerosis in the early stage of disease.
循环单核细胞在动脉粥样硬化发病机制中起着关键作用。单核细胞向动脉粥样硬化部位的归巢主要由选择素启动。因此,阻断选择素与其配体的相互作用在单核细胞归巢中起着重要作用,这可能是治疗动脉粥样硬化的一种潜在方法。在这里,我们研究了一种新型选择素配体 IELLQAR 类似肽在动脉粥样硬化中的疗效。
在这项研究中,我们首先通过流式细胞术测量了 IELLQAR 选择素结合肽对选择素与单核细胞结合的抑制作用,结果表明该肽对 P-、E-和 L-选择素与单核细胞的结合具有剂量依赖性抑制作用,尤其是对人外周血单核细胞(PBMCs)中 P-选择素结合的抑制作用(半最大抑制浓度(IC50))和 THP-1 细胞(IC10)。此外,IELLQAR 抑制了 P-选择素诱导的单核细胞表面 CD11b 的激活,并减少了单核细胞与内皮细胞的粘附,无论是在给予 Western 饮食(WTD)或血流紊乱引起的剪切力诱导的部分左侧颈动脉结扎(PLCA)以诱导动脉粥样硬化的小鼠中,还是在给予 IELLQAR(1 或 3mg/kg)的小鼠中。在 WTD 和 PLCA 诱导的动脉粥样硬化模型中,IELLQAR 肽处理的小鼠动脉壁中动脉粥样硬化斑块形成和单核细胞/巨噬细胞浸润均减少。我们的结果还表明,IELLQAR 通过 P-选择素依赖性激活核因子-(NF-)B 和哺乳动物雷帕霉素靶蛋白(mTOR)通路抑制单核细胞向巨噬细胞的分化。
总之,我们的结果表明,选择素配体的类似肽 IELLQAR 抑制了选择素与单核细胞的结合,从而通过抑制单核细胞的激活来减轻动脉粥样硬化。因此,使用 IELLQAR 肽提供了一种新的方法,并代表了治疗疾病早期动脉粥样硬化的一种有前途的候选药物。