Cell Physiology Laboratory, Institute of Biomedical Problems , Russian Academy of Sciences, Moscow, Russia .
Stem Cells Dev. 2018 Sep 15;27(18):1268-1277. doi: 10.1089/scd.2017.0264. Epub 2018 May 2.
Elucidation of the spaceflight (SF) effects on the adult stem and progenitor cells is an important goal in space biology and medicine. A unique opportunity for this was provided by project "BION-M1". The purpose of this study was to evaluate the effects of 30-day SF on biosatellite, 7-day recovery (SFR), and subsequent ground control (GC) experiment on the mononuclear cells (MNCs) from C57/BI/6N murine tibia bone marrow. Also, hematopoietic and stromal precursor functions were characterized ex vivo. There was no significant difference in the total MNC number between experimental groups. After SF, immunophenotyping revealed an increase of large-sized CD45MNCs corresponded to committed hematopoietic progenitors. The total hematopoietic colony-forming unit (CFU) number decreased after SF and did not restore after 7 day of recovery due to predominant reduction of bi- and multipotent CFUs and primitive burst-forming units in favor of unipotent CFUs. Functional activity of stromal precursors in vitro was only slightly altered. SF cells displayed the enhanced expression of alkaline phosphatase. The data of the GC experiment demonstrated the preservation of the functional activity of progenitor cells from mice bone marrow. The activation of erythropoiesis in expense of burst-forming units of erythrocytes elevation was detected. After 7 days of recovery, the number of colony-forming units of fibroblast (CFUs-f) was similar to the vivarium control, while the proliferative activity of bone marrow stromal precursors decreased. The present study demonstrated that certain hematopoietic progenitors are susceptible to SF factors, while the stromal precursors displayed a certain degree of resistance. These data indicate mild and reversible alterations of bone marrow progenitors after SF.
阐明太空飞行(SF)对成体干细胞和祖细胞的影响是空间生物学和医学的重要目标。项目“BION-M1”为此提供了一个独特的机会。本研究的目的是评估 30 天 SF 对生物卫星、7 天恢复(SFR)和随后的地面控制(GC)实验对 C57/BI/6N 小鼠胫骨骨髓单核细胞(MNC)的影响。此外,还对造血和基质前体细胞功能进行了体外特征描述。实验组之间的总 MNC 数量没有显著差异。SF 后免疫表型显示,与定向造血祖细胞相对应的大型 CD45MNC 数量增加。SF 后总造血集落形成单位(CFU)数量减少,7 天后恢复未恢复,原因是双能和多能 CFU 以及原始爆发形成单位减少,有利于单能 CFU。体外基质前体细胞的功能活性仅略有改变。SF 细胞显示碱性磷酸酶表达增强。GC 实验的数据表明,从小鼠骨髓中保留了祖细胞的功能活性。检测到以红细胞爆发形成单位升高为代价的红细胞生成激活。恢复 7 天后,成纤维细胞集落形成单位(CFUs-f)的数量与 vivarium 对照相似,而骨髓基质前体细胞的增殖活性降低。本研究表明,某些造血祖细胞易受 SF 因素影响,而基质前体细胞表现出一定程度的抗性。这些数据表明 SF 后骨髓祖细胞发生轻度和可逆的改变。