Davis T A, Wiesmann W, Kidwell W, Cannon T, Kerns L, Serke C, Delaplaine T, Pranger A, Lee K P
Immune Cell Biology Program, Stem Cell Biology Branch, Naval Medical Research Institute, Bethesda, Maryland 20889-5607, USA.
J Leukoc Biol. 1996 Jul;60(1):69-76. doi: 10.1002/jlb.60.1.69.
Humans subjected to periods of microgravity develop anemia, thrombocytopenia, and abnormalities in red blood cell structure. The causes of these abnormalities are complex and unclear. The in vitro effects of spaceflight on hematopoietic cell proliferation and differentiation were investigated during the space shuttle missions STS-63 (Discovery) and STS-69 (Endeavour). CD34+ bone marrow progenitor cells were cultured in liquid suspension culture and on hematopoietic supportive stromal cells using hollow-fiber culture modules. One set of cultures was maintained at microgravity (flight cultures) for the last 8-10 days of culture and a second control was at full gravity (ground control). Over the 11- to 13-test-day period, ground control culture total cell number increased 41.0- to 65.5-fold but flight culture total cell number increased only 10.1- to 17.6-fold (57-84% decrease). Comparing ground control cultures and microgravity cultures, respectively, for progenitor cell content, myeloid progenitor cell numbers expanded 2.6- to 17.5-fold compared with 0.9- to 7.0-fold and erythroid progenitor cell numbers expanded 2.0- to 4.1-fold in ground control cultures but actually declined at microgravity (>83% reduction). Moreover, microgravity cultures demonstrated accelerated maturation/differentiation toward the macrophage lineage. These data indicate that spaceflight has a direct effect on hematopoietic progenitor cell proliferation and differentiation and that specific aspects of in vitro hematopoiesis, particularly erythropoiesis, involve gravity-sensitive components.
经历微重力时期的人类会出现贫血、血小板减少以及红细胞结构异常。这些异常的原因复杂且不明。在航天飞机任务 STS - 63(发现号)和 STS - 69(奋进号)期间,研究了太空飞行对造血细胞增殖和分化的体外影响。使用中空纤维培养模块,将 CD34 + 骨髓祖细胞在液体悬浮培养中以及在造血支持性基质细胞上进行培养。一组培养物在培养的最后 8 - 10 天维持在微重力环境(飞行培养物),另一组对照在正常重力环境(地面对照)。在 11 至 13 天的测试期内,地面对照培养物的总细胞数增加了 41.0 至 65.5 倍,但飞行培养物的总细胞数仅增加了 10.1 至 17.6 倍(减少了 57 - 84%)。分别比较地面对照培养物和微重力培养物中的祖细胞含量,骨髓祖细胞数量在地面对照培养物中扩增了 2.6 至 17.5 倍,而在微重力环境下仅扩增了 0.9 至 7.0 倍;红系祖细胞数量在地面对照培养物中扩增了 2.0 至 4.1 倍,但在微重力环境下实际上减少了(减少超过 83%)。此外,微重力培养物显示出向巨噬细胞谱系的成熟/分化加速。这些数据表明太空飞行对造血祖细胞的增殖和分化有直接影响,并且体外造血的特定方面,特别是红细胞生成,涉及重力敏感成分。