Division of Endocrinology, Diabetes and Hypertension, Department of Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, MA, United States.
Department of Laboratory Medicine, Boston Children's Hospital, Boston, MA, United States.
Front Immunol. 2023 Feb 28;14:1124269. doi: 10.3389/fimmu.2023.1124269. eCollection 2023.
Major Histocompatibility Complex (MHC) molecules have been proposed to play a role in Sickle Cell Disease (SCD) pathophysiology. Endothelial cells express MHC molecules following exposure to cytokines. SCD is characterized, in part, by vascular endothelial cell activation, increased oxidative stress, sickle cell adhesion, and excess levels of endothelin-1 (ET-1) contributing to vaso-occlusive crises. ET-1 activates endothelial cells, induces oxidative stress and inflammation, and alters erythrocyte volume homeostasis. However, the role of ET-1 on MHC regulation in SCD is unclear. We first studied two sickle transgenic knockout mouse models of moderate to severe disease phenotype, βS-Antilles and Berkeley (BERK) mice. We observed significant increases in H2-Aa mRNA levels in spleens, lungs, and kidneys from transgenic sickle mice when compared to transgenic knockout mice expressing human hemoglobin A (HbA). Mice treated for 14 days with ET-1 receptor antagonists significantly reduced H2-Aa mRNA levels. We characterized the effect of ET-1 on MHC class II expression in the human endothelial cell line EA.hy926. We observed dose-dependent increases in the expression of MHC class II (HLA-DRA) and MHC transcription factor (CIITA) that were significantly blocked by treatment with BQ788, a selective blocker of ET-1 type B receptors. Chromatin immunoprecipitation studies in EA.hy926 cells showed that ET-1 increased Histone H3 acetylation of the HLA-DRA promoter, an event blocked by BQ788 treatment. These results implicate ET-1 as a novel regulator of MHC class II molecules and suggest that ET-1 receptor blockade represents a promising therapeutic approach to regulate both immune and vascular responses in SCD.
主要组织相容性复合体 (MHC) 分子被认为在镰状细胞病 (SCD) 的病理生理学中发挥作用。内皮细胞在细胞因子暴露后表达 MHC 分子。SCD 的特征部分是血管内皮细胞激活、氧化应激增加、镰状细胞黏附以及内皮素-1 (ET-1) 水平升高,导致血管阻塞危象。ET-1 激活内皮细胞,诱导氧化应激和炎症,并改变红细胞体积稳态。然而,ET-1 在 SCD 中对 MHC 调节的作用尚不清楚。我们首先研究了两种镰状转基因敲除小鼠模型,βS-Antilles 和 Berkeley (BERK) 小鼠。与表达人血红蛋白 A (HbA) 的转基因敲除小鼠相比,我们观察到转基因镰状小鼠的脾脏、肺和肾脏中 H2-Aa mRNA 水平显著增加。用 ET-1 受体拮抗剂治疗 14 天可显著降低 H2-Aa mRNA 水平。我们研究了 ET-1 对人内皮细胞系 EA.hy926 中 MHC Ⅱ类表达的影响。我们观察到 MHC Ⅱ类 (HLA-DRA) 和 MHC 转录因子 (CIITA) 的表达呈剂量依赖性增加,用选择性 ET-1 型 B 受体阻滞剂 BQ788 处理可显著阻断这种增加。EA.hy926 细胞中的染色质免疫沉淀研究表明,ET-1 增加了 HLA-DRA 启动子的组蛋白 H3 乙酰化,BQ788 处理可阻断该事件。这些结果表明 ET-1 是 MHC Ⅱ类分子的新型调节剂,并表明 ET-1 受体阻断剂代表了一种有前途的治疗方法,可调节 SCD 中的免疫和血管反应。