白血病细胞重塑骨髓 stromal 细胞,通过 S100A8-NOX2-ROS 信号通路产生突口微环境
Yangyang Gu1,2, Jingyi Xia3, Yuhong Guo1,2
1Department of Laboratory Medicine, School of Medical Technology and Engineering, Fujian Medical University, Fuzhou, Fujian, China.
Scientific reports
|May 17, 2025
概括
研究人员发现了急性髓性白血病 (AML) 细胞和骨髓 stromal 细胞 (BMSCs) 之间的通信通路. 针对S100A8可能通过破坏这种相互作用来为AML提供新的治疗策略.
科学领域:
- 血液学 血液学 血液学
- 癌症生物学 癌症生物学
- 细胞微环境 细胞微环境
背景情况:
- 骨髓微环境 (BMM) 在急性髓性白血病 (AML) 发病过程中至关重要.
- AML细胞操纵BMM以促进其生存,但确切的机制尚不清楚.
研究的目的:
- 研究骨髓 stromal 细胞 (BMSC) 和AML 细胞之间的相互作用的分子机制.
- 确定参与BMM-AML细胞通信的关键信号通路.
主要方法:
- 共同培养的AML细胞和BMSCs的蛋白质组分析.
- 研究了S100A8在细胞通信中的作用.
- 评估了反应性氧物种 (ROS) 生产及其影响.
- 利用细胞因子阵列和qPCR进行细胞因子分析.
主要成果:
- 共同培养促进了AML细胞的增殖,同时抑制和诱导BMSCs的衰老.
- 在AML细胞中异常S100A8表达激活NOX2,导致ROS产生.
- ROS抑制了BMSC的扩散,并诱导了衰老.
- 衰老的BMSCs分泌了刺激AML进展的细胞因子.
结论:
- 在S100A8-NOX2-ROS信号通路中介于AML细胞和BMSC之间的通信.
- 准S100A8为AML提供了一个潜在的治疗策略.
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