Bo Liu, Wei Luo, Ling Huang, Chunying Wei, Xiaorui Huang, Jun Liu, Ran Tao, Yingmin Mo, Xuebin Li
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引用次数: 0
摘要
外周免疫系统失调与阿尔茨海默病(AD)的神经炎症有关,并加速了疾病的进展。免疫细胞,尤其是 B 细胞,对阿尔茨海默病发病机制的贡献在最近的研究中备受关注。在这项研究中,我们基于 scRNA-seq 技术、免疫荧光和流式细胞术,研究了外周血记忆 B 细胞(PBMBs)及其分泌的迁移抑制因子(MIF)在驱动 AD 中巨噬细胞行为中的作用。我们发现,MIF 与巨噬细胞上的 CD74-CD44 受体复合物结合,影响巨噬细胞的行为。巨噬细胞反应失调阻碍了淀粉样蛋白-β(Aβ)斑块的清除,加剧了AD的病理变化。以MIF-CD74-CD44信号通路为靶点可能具有调节巨噬细胞活性和减轻AD神经炎症的治疗潜力。这项研究让人们进一步了解了AD中失调的外周免疫细胞。
Migration Inhibition Factor Secreted by Peripheral Blood Memory B Cells Binding to CD74-CD44 Receptor Complex Drives Macrophage Behavior in Alzheimer's Disease.
Dysregulation of the peripheral immune system is be involved in the neuroinflammation in Alzheimer disease (AD) and accelerate the disease progression. The contribution of immune cells, particularly B cells, to AD pathogenesis has gained attention in recent research. In this study, we investigated the role of Peripheral Blood Memory B cells (PBMBs) and their secreted Migration Inhibition Factor (MIF) in driving macrophage behavior in AD based on the scRNA-seq technique, immunofluorescence and flow cytometry. We discovered that MIF binds to the CD74-CD44 receptor complex on macrophages, influencing their behavior. The dysregulated macrophage response hampers the clearance of amyloid-beta (Aβ) plaques, exacerbating AD pathology. Targeting the MIF-CD74-CD44 signal pathway may hold therapeutic potential in modulating macrophage activity and mitigating neuroinflammation in AD. This study provides a further understanding of peripheral immune cells dysregulated in AD.