Canadian Nuclear Laboratories, Chalk River, ON, K0J 1 J0, Canada.
Regenerative Medicine Program, Ottawa Hospital Research Institute, 501 Smyth Rd., Box 704, Ottawa, ON, K1H 8L6, Canada.
Stem Cell Rev Rep. 2016 Apr;12(2):235-44. doi: 10.1007/s12015-015-9639-z.
The role of bone marrow-derived mesenchymal stem/stromal cells (MSCs) in creating a permissive microenvironment that supports the emergence and progression of acute myeloid leukemia (AML) is not well established. We investigated the extent to which adipogenic differentiation in normal MSCs alters hematopoietic supportive capacity and we undertook an in-depth comparative study of human bone marrow MSCs derived from newly diagnosed AML patients and healthy donors, including an assessment of adipogenic differentiation capacity.
MSCs from healthy controls with partial induction of adipogenic differentiation, in comparison to MSCs undergoing partial osteogenic differentiation, expressed increased levels of hematopoietic factors and induced greater proliferation, decreased quiescence and reduced in vitro hematopoietic colony forming capacity of CD34(+) hematopoietic stem and progenitor cells (HSPCs). Moreover, we observed that AML-derived MSCs had markedly increased adipogenic potential and delayed osteogenic differentiation, while maintaining normal morphology and viability. AML-derived MSCs, however, possessed reduced proliferative capacity and decreased frequency of subendothelial quiescent MSCs compared to controls.
Our results support the notion of a bone marrow microenvironment characterized by increased propensity toward adipogenesis in AML, which may negatively impact normal hematopoiesis. Larger confirmatory studies are needed to understand the impact of various clinical factors. Novel leukemia treatments aimed at normalizing bone marrow niches may enhance the competitive advantage of normal hematopoietic progenitors over leukemia cells.
骨髓间充质干细胞(MSCs)在创建一个允许的微环境中支持急性髓系白血病(AML)的出现和进展的作用尚未得到很好的确立。我们研究了正常 MSCs 中的脂肪生成分化在多大程度上改变了造血支持能力,并对来自新诊断的 AML 患者和健康供体的人骨髓 MSC 进行了深入的比较研究,包括对脂肪生成分化能力的评估。
与经历部分成骨分化的 MSCs 相比,接受部分诱导脂肪生成分化的健康对照者的 MSCs 表达更高水平的造血因子,并诱导 CD34+造血干细胞和祖细胞(HSPCs)的增殖增加、静止减少和体外造血集落形成能力降低。此外,我们观察到 AML 衍生的 MSC 具有明显增加的脂肪生成潜能和延迟的成骨分化,同时保持正常的形态和活力。然而,与对照组相比,AML 衍生的 MSC 增殖能力降低,亚内皮静止 MSC 的频率降低。
我们的结果支持 AML 中骨髓微环境具有增加的脂肪生成倾向的观点,这可能对正常造血产生负面影响。需要更大的确认性研究来了解各种临床因素的影响。旨在使骨髓龛正常化的新型白血病治疗方法可能会增强正常造血祖细胞对白血病细胞的竞争优势。