Quantitative imaging of haematopoietic stem and progenitor cell localization and hypoxic status in the bone marrow microenvironment

被引:392
作者
Nombela-Arrieta, Cesar [1 ]
Pivarnik, Gregory [1 ]
Winkel, Beatrice [1 ]
Canty, Kimberly J. [1 ]
Harley, Brendan [2 ]
Mahoney, John E. [3 ]
Park, Shin-Young [1 ]
Lu, Jiayun [1 ]
Protopopov, Alexei [3 ]
Silberstein, Leslie E. [1 ]
机构
[1] Childrens Hosp Boston, Dept Lab Med, Div Transfus Med, Boston, MA 02115 USA
[2] Univ Illinois, Dept Chem & Biomol Engn, Urbana, IL 61801 USA
[3] Dana Farber Canc Inst, Div Hematol Malignancies, Boston, MA 02115 USA
关键词
SELF-RENEWAL; NICHES; OXYGEN; DIFFERENTIATION; IDENTIFICATION; HIF-1-ALPHA; BALANCE; RESIDE;
D O I
10.1038/ncb2730
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The existence of a haematopoietic stem cell niche as a spatially confined regulatory entity relies on the notion that haematopoietic stem and progenitor cells (HSPCs) are strategically positioned in unique bone marrow microenvironments with defined anatomical and functional features. Here, we employ a powerful imaging cytometry platform to perform a comprehensive quantitative analysis of HSPC distribution in bone marrow cavities of femoral bones. We find that HSPCs preferentially localize in endosteal zones, where most closely interact with sinusoidal and non-sinusoidal bone marrow microvessels, which form a distinctive circulatory system. In situ tissue analysis reveals that HSPCs exhibit a hypoxic profile, defined by strong retention of pimonidazole and expression of HIF-1 alpha, regardless of localization throughout the bone marrow, adjacency to vascular structures or cell-cycle status. These studies argue that the characteristic hypoxic state of HSPCs is not solely the result of a minimally oxygenated niche but may be partially regulated by cell-specific mechanisms.
引用
收藏
页码:533 / +
页数:20
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