调控网络架构限制了组织居民膜巨细胞中的炎症反应
bioRxiv : the preprint server for biology
|February 27, 2026
概括
组织寄存型巨细胞显示抑制的炎症反应,这是由于稳定基因调节网络涉及PU.1和CEBP/β转录因子. 这突显了它们在宿主防御和功能性可塑性中的独特作用.
科学领域:
- 免疫学 免疫学 免疫学
- 基因组学就是基因组学.
- 系统生物学 系统生物学
背景情况:
- 巨细胞在各个组织中表现出多样化的功能,由复杂的基因调节网络控制.
- 了解协调组织居民巨细胞身份和炎症的高级调节相互作用至关重要,但有限.
研究的目的:
- 在炎症性压力下推断组织居民与招募的膜巨细胞中的基因调控网络架构.
- 阐明功能性可塑性和巨细胞的差异性炎症反应背后的机制.
主要方法:
- 单细胞RNA-seq和ATAC-seq数据的整合.
- 基于深度学习的染色体可访问性建模.
- 对基因调节网络的比较分析.
主要成果:
- 在组织居民和招募的膜巨细胞之间确定了不同的基因调节网络架构.
- 已经证明,在组织寄存的巨细胞中,炎症反应更加克制.
- 突出了PU.1和CEBP/β在组织居民巨细胞的调节网络中的稳定作用.
结论:
- 涉及PU.1和CEBP/β的稳定性调节网络有助于抑制组织居民巨细胞的炎症.
- 这项研究促进了对组织寄存巨细胞功能性可塑性的理解.
- 阐明了这些巨细胞在宿主防御调节中的作用.
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