首页> 外文期刊>Innate immunity >Immunization with malondialdehyde-modified low-density lipoprotein (LDL) reduces atherosclerosis in LDL receptor-deficient mice challenged with Porphyromonas gingivalis
【24h】

Immunization with malondialdehyde-modified low-density lipoprotein (LDL) reduces atherosclerosis in LDL receptor-deficient mice challenged with Porphyromonas gingivalis

机译:丙二醛修饰的低密度脂蛋白(LDL)免疫减少了牙龈卟啉单胞菌攻击的LDL受体缺陷小鼠的动脉粥样硬化

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

Periodontal infections increase the risk of atherosclerotic vascular disease via partly unresolved mechanisms. Of the natural IgM Abs that recognize molecular mimicry on bacterial epitopes and modified lipid and protein structures, IgM directed against oxidized low-density lipoprotein (LDL) is associated with atheroprotective properties. Here, the effect of natural immune responses to malondialdehyde-modified LDL (MDA-LDL) in conferring protection against atherosclerosis, which was accelerated by the major periodontopathogen Porphyromonas gingivalis, was investigated. LDL receptor-deficient (LDLR-/-) mice were immunized with mouse MDA-LDL without adjuvant before topical application challenge with live P. gingivalis. Atherosclerosis was analyzed after a high-fat diet, and plasma IgG and IgM Ab levels were measured throughout the study, and the secretion of IL-5, IL-10 and IFN- in splenocytes stimulated with MDA-LDL was determined. LDLR-/- mice immunized with MDA-LDL had elevated IgM and IgG levels to MDA-LDL compared with saline-treated controls. MDA-LDL immunization diminished aortic lipid depositions after challenge with P. gingivalis compared with mice receiving only P. gingivalis challenge. Immunization of LDLR-/- mice with homologous MDA-LDL stimulated the production of IL-5, implicating general activation of B-1 cells. Immune responses to MDA-LDL protected from the P. gingivalis-accelerated atherosclerosis. Thus, the linkage between bacterial infectious burden and atherogenesis is suggested to be modulated via natural IgM directed against cross-reactive epitopes on bacteria and modified LDL.
机译:牙周感染通过部分尚未解决的机制增加了动脉粥样硬化性血管疾病的风险。在识别细菌表位上的分子模拟以及修饰的脂质和蛋白质结构的天然IgM Ab中,针对氧化型低密度脂蛋白(LDL)的IgM具有抗动脉粥样硬化特性。在这里,研究了对丙二醛修饰的低密度脂蛋白(MDA-LDL)的天然免疫反应在保护动脉粥样硬化中的作用,该作用被主要的牙周病原体牙龈卟啉单胞菌所加速。在没有佐剂的情况下,用小鼠MDA-LDL免疫LDL受体缺陷(LDLR-/-)小鼠,然后用活牙龈卟啉单胞菌局部应用激发。高脂饮食后分析动脉粥样硬化,并在整个研究过程中测量血浆IgG和IgM Ab水平,并测定MDA-LDL刺激的脾细胞中IL-5,IL-10和IFN-的分泌。与盐水处理的对照组相比,用MDA-LDL免疫的LDLR-/-小鼠的Mg-LDL的IgM和IgG水平升高。与仅接受牙龈卟啉单胞菌攻击的小鼠相比,MDA-LDL免疫减少了牙龈卟啉单胞菌攻击后的主动脉脂质沉积。用同源MDA-LDL免疫LDLR-/-小鼠刺激了IL-5的产生,暗示了B-1细胞的普遍活化。对MDA-LDL的免疫反应可预防牙龈卟啉单胞菌加速的动脉粥样硬化。因此,建议通过针对细菌和修饰的LDL上的交叉反应性表位的天然IgM来调节细菌感染负担和动脉粥样硬化之间的联系。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号