在高脂血症小鼠中,G蛋白结合受体91依赖信号不影响血管炎症和动脉样硬化
Silke Griepke1, Mette Trauelsen2, Michelle D Nilsson1
1Department of Cardiovascular and Renal Research, Institute of Molecular Medicine, University of Southern Denmark, 5000 Odense, Denmark.
Cells
|November 10, 2023
概括
通过其受体GPR91作用的酸盐被研究其在动脉样硬化中的作用. 在小鼠中,GPR91的切除没有影响动脉样硬化或血管炎症的发展.
科学领域:
- 心血管研究研究心血管研究
- 免疫学 免疫学 免疫学
- 代谢过程中的代谢.
背景情况:
- 酸盐是一种TCA循环代谢物,被认为是一种炎症调解剂.
- 它的受体SUCNR1/GPR91参与自身免疫和过敏反应.
- 在动脉样硬化等慢性炎症性疾病中GPR91信号的作用仍然未被探索.
研究的目的:
- 研究GPR91介导信号对动脉样硬化的慢性炎症过程的影响.
- 为了确定GPR91信号是否影响血管炎症和动脉生成.
主要方法:
- 对SUCNR1基因表达的人类动脉样硬化斑块数据集的分析.
- 使用GPR91淘汰和野生型小鼠,通过Pcsk9过度表达和西方饮食诱导高脂血症.
- 评估动脉样硬化病变的大小,巨细胞透和巨细胞两极分化.
主要成果:
- 在人类动脉样硬化斑块中检测到SUCNR1基因表达,特别是在血管光滑肌细胞中.
- 完全切除GPR91并没有加速大动脉门或超脂血小鼠根部的动脉样硬化.
- 在巨细胞或T细胞透,以及GPR91淘汰和野生类型小鼠之间的巨细胞两极分化方面没有观察到显著差异.
结论:
- 全球废除GPR91信号似乎没有影响血管炎症或动脉样硬化的发展.
- 这些发现表明GPR91可能不是动脉样硬化病变的关键调解者.
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