人类骨髓脂肪组织是白素驱动的单形成的血液形成基因
bioRxiv : the preprint server for biology
|September 11, 2023
概括
老化骨髓脂肪组织扩大,创造了一个促进炎症的利基. 这种利基通过勒丁信号刺激单细胞的产生,可能导致炎症.
科学领域:
- 血液学 血液学 血液学
- 免疫学 免疫学 免疫学
- 衰老研究研究 衰老研究
背景情况:
- 骨髓脂肪组织 (BMAT) 随着年龄的增长而扩大,而红髓则收缩.
- BMAT扩张对造血和炎症的功能影响尚不清楚.
研究的目的:
- 为了研究丰富脂肪的黄色骨髓 (BMY) 和缺乏脂肪的红色骨髓 (BMR) 中独特的造血.
- 阐明BMAT在骨髓与年龄相关的炎症变化中的作用.
主要方法:
- 对人类BMY和BMR的单细胞和单核转录组分析.
- 开发和利用人体骨髓器官系统.
- 分析瘦素受体表达和瘦素刺激的细胞增殖和分化.
主要成果:
- 确定了两个不同的造血;BMY拥有更多的单细胞和与炎症相关的原生细胞.
- BMY细胞表现出明显的瘦素受体表达,并通过增加增殖和单细胞生产来响应瘦素.
- 骨髓脂肪组织是造血干细胞和祖细胞的利基,通过勒丁信号传递驱动亲炎性单细胞的产生.
结论:
- 骨髓脂肪组织与年龄相关的扩张促进了亲炎症状态.
- 在BMAT中传递勒素信号刺激了来自特定的造血干细胞和原生细胞群的单细胞生产.
- 这种机制可能会导致炎症,与衰老相关的慢性轻度炎症.
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