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载脂蛋白 E 和 Fas 配体双重缺陷 C57BL/6 小鼠中 I 型干扰素与内皮祖细胞耗竭和功能障碍的关系。

Association between Type I interferon and depletion and dysfunction of endothelial progenitor cells in C57BL/6 mice deficient in both apolipoprotein E and Fas ligand.

机构信息

Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, 321 Zhongshan Road, Nanjing 210008, China.

Key Laboratory of Model Animal for Disease Study, Model Animal Research Center, Nanjing University, 12 Xuefu Road, Nanjing 210000, China.

出版信息

Curr Res Transl Med. 2018 Sep;66(3):71-82. doi: 10.1016/j.retram.2018.02.002. Epub 2018 Aug 11.

Abstract

Patients with systemic lupus erythematosus (SLE) have a tremendously increased risk for cardiovascular disease (CVD), which could not be accounted in entirety by traditional Framingham risk factors. To study whether the accelerated atherosclerosis in SLE patients is mediated by type I interferon (IFN-I) through the regulation of endothelial progenitor cells (EPCs), we created a line of C57BL/6 mice with deficiency in both apolipoprotein E (ApoE-/-) and fas ligand (FasL-/-, gld.). As expected, the resultant gld. ApoE-/- mice exhibited both aggravated lupus-like disease and atherosclerosis under normal diet. Increased expression of IFN-I-stimulated genes (ISGs) was closely associated with depletion and dysfunction of EPCs, as well as with accelerated atherosclerotic lesion in gld. ApoE-/- mice. While only IFN-α instead of other interventions, including tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), IRS423 and IRS661, impaired EPC function in vitro. Mechanistically, activation or inhibition of the TLR7/9 signaling could modulate EPC number and function in vivo. Decreased proliferation rate and increased apoptotic rate of EPCs induced by IFN-α might contribute to the results to a certain extent. Thus, our data suggest that excessive expression of IFN-I through the activation of TLR7/9 signaling may induce accelerated atherosclerosis in lupus through the depletion or dysfunction of EPCs, suggesting that targeting IFN-I might have potential therapeutic effects on both lupus disease and premature atherosclerosis in SLE patients.

摘要

系统性红斑狼疮 (SLE) 患者发生心血管疾病 (CVD) 的风险极高,这不能完全用传统的弗莱明翰风险因素来解释。为了研究 SLE 患者的动脉粥样硬化是否是通过 I 型干扰素 (IFN-I) 通过调节内皮祖细胞 (EPCs) 而加速的,我们构建了一种 C57BL/6 小鼠,其载脂蛋白 E (ApoE-/-) 和 Fas 配体 (FasL-/-,gld.) 均缺失。正如预期的那样,在正常饮食下,gld. ApoE-/- 小鼠表现出更严重的狼疮样疾病和动脉粥样硬化。IFN-I 刺激基因 (ISGs) 的表达增加与 EPCs 的耗竭和功能障碍密切相关,并与 gld. ApoE-/- 小鼠的动脉粥样硬化病变加速有关。虽然只有 IFN-α而不是其他干预措施,包括肿瘤坏死因子-α (TNF-α)、白细胞介素-1β (IL-1β)、IRS423 和 IRS661,会损害体外 EPC 功能。在机制上,TLR7/9 信号的激活或抑制可以调节体内 EPC 的数量和功能。IFN-α诱导的 EPC 增殖率降低和凋亡率增加可能在一定程度上导致了这些结果。因此,我们的数据表明,通过激活 TLR7/9 信号,IFN-I 的过度表达可能通过 EPCs 的耗竭或功能障碍导致狼疮加速动脉粥样硬化,表明靶向 IFN-I 可能对 SLE 患者的狼疮疾病和早发性动脉粥样硬化具有潜在的治疗效果。

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