南方医科大学学报2017，Vol.37Issue(8)：1003-1009,7.DOI:10.3969/j.issn.1673-4254.2017.08.01
吡格列酮通过调控TGF-β信号通路和T细胞调节性免疫机制缓解ApoE-/-小鼠动脉粥样硬化
Pioglitazone ameliorates atherosclerosis in apoE knockout mice through transforming growth factor-β/Smad signaling and adaptive T cell immunity
摘要
Abstract
Objective To examine whether transforming growth factor-β (TGF-β) pathway and adaptive T cell immunity play roles in the anti-atherosclerotic effects of pioglitazone (PIO) in ApoE-/-mice. Methods ApoE-/-mice with atherosclerosis induced by high-fat feeding were treated daily with PIO (20 mg/kg) or vehicle for 8 weeks. The protein expressions of TGF-βpathway in the atheromatous lesions of the aorta and the percentages of IFN-γ+and Foxp3+cells in the spleen of the mice were examined with immunohistochemical staining. In the in vitro experiment, primary cultured splenocytes were stimulated with oxidized low-density lipoproteins (oxLDL) and treated with PIO either alone or in combination with the PPARγ antagonist GW9662, after which the changes in percentages of CD4+IFN-γ+cells and CD4+CD25+Foxp3+cells were analyzed with flow cytometry. Results PIO treatment of ApoE-/-mice with high-fat feeding significantly attenuated the progression of atheromatous lesions (P<0.05) and resulted in increased expressions of TGFβ1 (P<0.01), TGFβRII (P<0.05), and p-Smad3 (P<0.05) and a decreased expression of Smad7 (P<0.05) in the lesions. PIO treatment also led to decreased percentage of IFN-γ + cells (P<0.05) and increased percentage of Foxp3+cells (P<0.01) in the spleen of the mice. In primary cultured splenocytes, PIO treatment caused significant down-regulation of IFN-γmRNA (P<0.05) and up-regulation of Foxp3 mRNA (P<0.05) and obviously increased the percentages of CD4+IFN-γ+cells (P<0.05) and CD4+CD25+Foxp3+(P<0.05);the effects of PIO on CD4+IFN-γ+and CD4+CD25+Foxp3 + cells were abolished by treatment of the cells with GW9662. Conclusion The anti-atherosclerotic effect of PIO is probably mediated by the TGF-β/Smad signaling pathway and PPAR-γ-dependent modulation of Th1/Treg population.关键词
吡格列酮/PPARγ/T细胞/TGF-β/Smad信号通路/动脉粥样硬化Key words
pioglitazone/nuclear receptor peroxisome proliferator-activated receptor-γ/T cells/transforming growth factor-β/Smad signaling/atherosclerosis引用本文复制引用
田雨灵,王丽君,吴岳,张卫萍,梁潇,袁祖贻..吡格列酮通过调控TGF-β信号通路和T细胞调节性免疫机制缓解ApoE-/-小鼠动脉粥样硬化[J].南方医科大学学报,2017,37(8):1003-1009,7.基金项目
Supported by National Natural Science Foundation of China (81300226) and National Natural Science Fund for Distinguished Young Scholars (81025002).国家自然科学基金(81300226) （81300226）
国家杰出青年科学基金(81025002) （81025002）
