造血
骨髓生成
细胞生物学
骨髓
间质细胞
炎症
生物
再生(生物学)
干细胞
祖细胞
促炎细胞因子
免疫学
间充质干细胞
癌症研究
作者
Carl A. Mitchell,Evgenia Verovskaya,Fernando J. Calero‐Nieto,Oakley C. Olson,James W. Swann,Xiaonan Wang,Aurélie Herault,Paul V. Dellorusso,Si Yi Zhang,Arthur Flohr Svendsen,Eric M. Pietras,Sietske T. Bakker,Theodore Ho,Berthold Göttgens,Emmanuelle Passegué
标识
DOI:10.1038/s41556-022-01053-0
摘要
Haematopoietic ageing is marked by a loss of regenerative capacity and skewed differentiation from haematopoietic stem cells (HSCs), leading to impaired blood production. Signals from the bone marrow niche tailor blood production, but the contribution of the old niche to haematopoietic ageing remains unclear. Here we characterize the inflammatory milieu that drives both niche and haematopoietic remodelling. We find decreased numbers and functionality of osteoprogenitors at the endosteum and expansion of central marrow LepR
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