Spatial gradients of blood vessels and hematopoietic stem and progenitor cells within the marrow cavities of the human skeleton

被引:36
作者
Bourke, Vincent A. [2 ]
Watchman, Christopher J. [2 ]
Reith, John D. [3 ]
Jorgensen, Marda L. [3 ]
Dieudonne, Arnaud [4 ]
Bolch, Wesley E. [1 ,5 ]
机构
[1] Univ Florida, Dept Nucl & Radiol Engn, Adv Lab Radiat Dosimetry Studies, Nucl Sci Ctr 202, Gainesville, FL 32611 USA
[2] Univ Arizona, Dept Radiat Oncol, Tucson, AZ 85721 USA
[3] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
[4] Univ Rouen, LITIS Lab, Rouen, France
[5] Univ Florida, Dept Biomed Engn, Gainesville, FL 32611 USA
关键词
NICHE; IDENTIFICATION; BONE;
D O I
10.1182/blood-2008-12-192922
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
This report evaluates the spatial profile of blood vessel fragments (BVFs) and CD34(+) and CD117(+) hematopoietic stem and progenitor cells (HSPCs) in human cancellous bone. Bone specimens were sectioned, immunostained (anti-CD34 and anti-CD117), and digitally imaged. Immunoreactive cells and vessels were then optically and morphometrically identified and labeled on the corresponding digital image. The distance of each BVF, or CD34(+) or CD117(+) HSPC to the nearest trabecular surface was measured and binned in 50-mu m increments. The relative concentration of HSPCs and BVFs within cancellous marrow was observed to diminish with increasing distance in the marrow space. On average, 50% of the CD34(+) HSPC population, 60% of the CD117(+) HSPC population, and 72% of the BVFs were found within 100 mu m of the bone surfaces. HSPCs were also found to exist in close proximity to BVFs, which supports the notion of a shared HSPC and vessel spatial niche. (Blood. 2009; 114: 4077-4080)
引用
收藏
页码:4077 / 4080
页数:4
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