Department of Pediatrics, Division of Hematology and Oncology, University of Florida College of Medicine, Gainesville, Florida, USA.
Exp Hematol. 2013 Jul;41(7):635-645.e3. doi: 10.1016/j.exphem.2013.03.003. Epub 2013 Mar 15.
Sublethal irradiation and 5-fluorouracil (5-FU) treatment are two commonly used myelosuppressive methods used in the study of hematopoiesis. These methods have been considered interchangeable by some researchers because the morphological changes in the bone marrow to these treatments are similar. Here, we sought to compare the responses of hematopoietic cells, stem and progenitor cells and the bone marrow microenvironment to these treatments. Although bone marrow cellularity decreased after both treatments, the underlying mechanism of the bone marrow cell regression and recovery were very different between the two models. We found: 1. Myeloid cells and lymphoid cells had different sensitivity to the different treatments. 2. Following an initial decrease in stem cell number, 5-FU treated mice had profound thrombopoietin (Tpo) dependent stem cell rebound above baseline levels. 3. Platelet rebound in 5-FU treated animals was not the result of stem cell rebound. 4. Stem cell and platelet rebound did not occur in sub-lethally irradiated mice. 5. Platelet rebound resulted from an indirect effect of 5-FU on the microenvironment cells, but not a direct effect on the stem cells. 6. Microarray studies demonstrated that up-regulation of the angiopoietin-1/Tie2 signaling pathway coincided with platelet rebound. 7. Suppression of genes involved in chromosomal organization coincided with stem cell and platelet rebound.
亚致死辐射和 5-氟尿嘧啶(5-FU)处理是两种常用于造血研究的常用骨髓抑制方法。由于这些治疗方法对骨髓的形态变化相似,一些研究人员认为它们可以互换。在这里,我们试图比较这些治疗方法对造血细胞、干细胞和祖细胞以及骨髓微环境的反应。尽管两种治疗方法后骨髓细胞数量均减少,但两种模型中骨髓细胞消退和恢复的潜在机制却大不相同。我们发现:1. 髓系细胞和淋巴系细胞对不同的治疗方法有不同的敏感性。2. 在干细胞数量最初减少后,5-FU 处理的小鼠中存在严重的血小板生成素(Tpo)依赖性干细胞反弹,超过基线水平。3. 5-FU 处理动物的血小板反弹不是干细胞反弹的结果。4. 亚致死辐射小鼠中未发生干细胞和血小板反弹。5. 血小板反弹是 5-FU 对微环境细胞的间接作用的结果,而不是对干细胞的直接作用。6. 微阵列研究表明,血管生成素-1/Tie2 信号通路的上调与血小板反弹相一致。7. 涉及染色体组织的基因抑制与干细胞和血小板反弹相一致。