内皮编程死亡-1连接体1 (PD-L1) 调节心脏中CD8+T细胞介导的损伤
Nir Grabie1, Israel Gotsman, Rosa DaCosta
1Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Circulation
|October 17, 2007
概括
在心脏内皮细胞上编程的死亡连接体1 (PD-L1) 对于控制免疫媒介心脏损伤至关重要. 失去PD-L1信号会通过促进多态核白细胞炎症而加剧心肌炎.
科学领域:
- 免疫学 免疫学 免疫学
- 心脏病学 心脏病学
- 分子生物学分子生物学
背景情况:
- 编程死亡-1 (PD-1) 是一种调节免疫反应的抑制受体.
- 在炎症期间,PD-1的配体PD-L1在心脏内皮细胞上被诱导.
- 对于PD-L1在心脏免疫损伤中的作用尚不清楚.
研究的目的:
- 调查PD-L1信号在细胞毒性T淋巴细胞介导心肌炎中的作用.
- 在炎症期间确定心脏PD-L1的细胞源和功能.
主要方法:
- 在小鼠中诱导心肌炎.
- 使用了PD-L1/L2缺乏的小鼠和阻断抗体.
- 分析了免疫细胞透和疾病严重程度.
主要成果:
- 对心脏内皮的PD-L1上调取决于干扰素-.
- 阻断PD-L1信号传输或其配体导致致命的心肌炎.
- 在非骨髓衍生细胞上的PD-L1给予了保护.
- 多态核白细胞枯竭逆转了疾病恶化.
结论:
- 心肌PD-L1,主要在内皮上,对于控制免疫媒介心脏损伤至关重要.
- PD-L1在调节心脏中的多态核白细胞炎症方面发挥着关键作用.
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