Department of Genetics, Cell Biology and Anatomy, University of Nebraska Medical Center, Omaha, NE, USA.
Pharmacy Practice, University of Nebraska Medical Center, Omaha, NE, USA.
Exp Hematol. 2014 Feb;42(2):146-54. doi: 10.1016/j.exphem.2013.11.003. Epub 2013 Nov 15.
This study enumerated CD45(hi)/CD34(+) and CD45(hi)/CD133(+) human hematopoietic stem cells (HSCs) and progenitor granulocyte-macrophage colony forming cells (GM-CFCs) in blood and trochanteric and femoral bone marrow in 233 individuals. Stem cell frequencies were determined with multiparameter flow cytometry and using an internal control to determine the intrinsic variance of the assays. Progenitor cell frequency was determined using a standard colony assay technique. The frequency of outliers from undetermined methodological causes was highest for blood, but less than 5% for all values. The frequency of CD45(hi)/CD133(+) cells correlated highly with the frequency of CD45(hi)/CD34(+) cells in trochanteric and femoral bone marrow. The frequency of these HSC populations in trochanteric and femoral bone marrow rose significantly with age. In contrast, there was no significant trend of either of these cell populations with age in the blood. Trochanteric marrow progenitor GM-CFCs showed no significant trends with age, but femoral marrow GM-CFCs trended downward with age, potentially because of the reported conversion of red marrow at this site to fat with age. Hematopoietic stem and progenitor cells exhibited changes in frequencies with age that differed between blood and bone marrow. We previously reported that side population (SP) multipotential HSC, which includes the precursors of CD45(hi)/CD133(+) and CD45(hi)/CD34(+), decline with age. Potentially the increases in stem cell frequencies in the intermediate compartment between SP and GM progenitor cells observed in this study represent a compensatory increase for the loss of more potent members of the HSC hierarchy.
本研究在 233 个人中列举了血液、转子和股骨骨髓中的 CD45(hi)/CD34(+) 和 CD45(hi)/CD133(+) 人造血干细胞 (HSC) 和祖粒细胞-巨噬细胞集落形成细胞 (GM-CFC)。使用多参数流式细胞术和内部对照来确定测定的固有变异性,确定干细胞频率。使用标准集落测定技术确定祖细胞频率。由于方法原因无法确定的离群值频率在血液中最高,但所有值的频率均低于 5%。转子和股骨骨髓中 CD45(hi)/CD133(+)细胞的频率与 CD45(hi)/CD34(+)细胞的频率高度相关。转子和股骨骨髓中这些 HSC 群体的频率随着年龄的增长而显著升高。相比之下,血液中这些细胞群体的频率没有随着年龄的增长而呈现出显著的趋势。转子骨髓祖 GM-CFC 随年龄没有明显变化趋势,但股骨骨髓 GM-CFC 随年龄呈下降趋势,可能是因为该部位的红骨髓随着年龄的增长转化为脂肪。造血干细胞和祖细胞的频率随年龄变化,血液和骨髓之间存在差异。我们之前报道过侧群 (SP) 多潜能 HSC 随年龄下降,其中包括 CD45(hi)/CD133(+) 和 CD45(hi)/CD34(+) 的前体。研究中观察到的 SP 和 GM 前体细胞之间中间隔室中干细胞频率的增加可能代表了对 HSC 等级中更有效成员丧失的代偿性增加。