缺血损伤通过加速的造血衰老驱动瘤生长
bioRxiv : the preprint server for biology
|July 14, 2025
概括
周围缺血症通过促进造血干细胞 (HSC) 炎症加速乳腺癌. 这导致免疫反应发生变化和瘤生长速度加快,其影响可以通过骨髓移植传播.
科学领域:
- 免疫学 免疫学 免疫学
- 在瘤学瘤学.
- 血液学 血液学 血液学
背景情况:
- 周围动脉疾病 (PAD) 与癌症风险增加有关.
- 造血干细胞和原生细胞 (HSPC) 的与衰老相关的变化有助于心血管疾病 (CVD) 和癌症.
- 改变血液形成在心血管疾病驱动的瘤进展中的作用仍然不清楚.
研究的目的:
- 在周围缺血症后调查癌症生长.
- 分析HSPC骨髓部分的变化.
- 揭示了将改变的血液形成与瘤发生联系在一起的机制.
主要方法:
- 监测小鼠的乳腺癌细胞生长后后肢缺血症 (HLI) 或假手术.
- 通过流细胞计量评估瘤免疫微环境,循环免疫细胞和HSPC区.
- 在HSPC上进行单细胞RNA和ATAC测序;进行骨髓移植.
主要成果:
- HLI增加了单细胞/中性粒细胞的产量,减少了淋巴细胞,这是由骨髓偏差HSC驱动的.
- 观察到乳腺癌的加速生长和免疫抑制细胞 (Tregs,单细胞) 的增加.
- 多原子分析揭示了HLI诱导的祖先的炎症和衰老特征;影响是通过骨髓移植传播的.
结论:
- 周围缺血促进HSC炎症和持久的抗瘤免疫改变.
- 这一过程加速了乳腺瘤的生长.
- 长期对天生的免疫反应进行重新编程,有助于加速瘤发生.
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