单细胞转录组分析揭示了MIF对多发性骨髓瘤中髓衍生的抑制细胞的影响
XiaoDong Zhao1, JingXin Zhou1, JinRong Yao1
1Department of Hematology, The Affiliated Suqian First People's Hospital of Nanjing Medical University, SuQian, Jiangsu, China.
International journal of laboratory hematology
|April 3, 2025
概括
巨细胞迁移抑制因子 (MIF) 在多发性骨髓瘤 (MM) 患者中升高,与骨髓中的骨髓衍生抑制细胞 (MDSC) 相对应. 本研究确定了不同的MIF表达MDSC子集及其在MM中的通信途径.
科学领域:
- 免疫学 免疫学 免疫学
- 血液学 血液学 血液学
- 癌症生物学 癌症生物学
背景情况:
- 多发性髓瘤 (MM) 是一种致命的血液性恶性瘤.
- 骨髓衍生抑制细胞 (MDSCs) 显著影响MM骨髓微环境.
- 巨细胞迁移抑制因子 (MIF) 是一种调节免疫反应的炎症性细胞因子.
研究的目的:
- 调查MM骨髓微环境中的MIF和MDSC之间的关系.
- 在MM患者中描述表达MIF的MDSC子集.
主要方法:
- 单细胞RNA测序 (scRNA-seq) 的MM和正常样本 (GSE124310数据集).
- 使用CellMarker 2.0.0进行细胞类型注释.
- 使用CellChat推断细胞细胞通信通路.
- 流细胞计用于表征细胞标记物.
主要成果:
- scRNA-seq确定了10个细胞子集,MDSC根据MIF表达被分为MIF+和MIF-子集.
- 在MM和正常组之间观察到MIF+和MIF-MDSC的不同比例.
- MIF+ MDSCs显示了低的RETN-CAP1通路与血细胞的信号传递,而MIF-MDSCs显示了高的信号传递.
- 流细胞计证实了MM MDSCs中RETN,Arg-1和iNOS的增加,在MIF+MDSC中表达更高. 在MM血细胞中,CAP1升高.
结论:
- 在MM患者中,MIF是上调调的.
- 在MM骨髓微环境中,MIF表达与MDSC相关.
- 不同的MDSC子集及其通信途径,如RETN-CAP1,与MM进展有关.
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