[免疫介导的再生障碍性贫血模型小鼠巨噬细胞的归巢及特征分析]

W Sun, Z H Lin, H Wang, H Jia, L G Tong, Z P Zhang, W Li, C C Zhou, H Liu
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引用次数: 0

摘要

研究免疫介导的再生障碍性贫血(AA)模型小鼠不同器官中巨噬细胞的动态归巢过程和特征。用磁珠分选供体淋巴结中的巨噬细胞并用 PKH67 标记。按照 AA 模型的制备方法建模后,分析外周血红细胞分析、骨髓活检和 HE 染色结果以验证建模效果。建模第4、8和12天,收集供体小鼠的骨髓、脾脏和淋巴结单核细胞,用流式细胞术分析供体小鼠体内PKH67标记的巨噬细胞的动态变化。本研究探讨了PKH67标记的巨噬细胞在AA模型小鼠发病过程中的动态变化。供体小鼠的巨噬细胞归巢到淋巴结,在淋巴结中扩增和分化,最后转运到骨髓和脾脏。通过蛋白质组学质谱分析,初步揭示了巨噬细胞参与激活AA骨髓微环境的相关免疫炎症反应途径,为AA模型小鼠发病机制中病理巨噬细胞的参与提供了依据。
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[Homing and characteristic analysis of macrophage in immune-mediated aplastic anemia model mice].

To investigate the dynamic homing process and characteristics of macrophages in different organs of immune-mediated aplastic anemia (AA) model mice. Macrophages in donor lymph nodes were sorted by magnetic beads and labeled with PKH67. After modeling according to the preparation method of the AA model, peripheral blood rountine analysis, bone marrow biopsy and HE staining results were analyzed to verify the modeling effect. On days 4, 8, and 12 of modeling, the bone marrow, spleen, and lymph node mononuclear cells were collected, and dynamic changes of PKH67-labeled macrophages in donor mice were analyzed by flow cytometry. In this study, dynamic changes in PKH67-labeled macrophages in the pathogenesis of AA model mice were explored. Macrophages in donor mice homed to the lymph nodes, expanding and differentiating in the lymph nodes, and finally transported to the bone marrow and spleen. Through proteomics mass spectrometry analysis, the related immune inflammatory response pathway of macrophages involved in the activation of the AA bone marrow microenvironment was preliminarily revealed, which provides a basis for the pathological macrophages involved in the pathogenesis of AA model mice.

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CiteScore
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发文量
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