Austin T, Ma A, Datta M C, Ortega J A, Shore N A, Dukes P P
Exp Hematol. 1979 Feb;7(2):63-73.
The effect of L1210 transplantable leukemic cells on in vitro formation of erythroid colonies from CD2F1 mouse bone marrow progenitor cells (CFU-E) was investigated. Clonal cell culture was carried out by a methylcellulose technique. Human urinary erythropoietin served as the stimulator. After 44 hours of incubation aggregates of eight or more erythroid cells were scored as colonies. The number of CFU-E which could be demonstrated in marrow cells from mice that had been injected intravenously 6 days before with 5 x 10(4) L1210 cells was far below that obtained from normal marrow cells. When 1.3 x 10(5) marrow cells from leukemic mice or L1210 ascites cells were cultured with an equal amount of normal cells, the number of CFU-E expressed was reduced by 51% and by 86%, respectively, relative to controls with normal cells only. Neither lethally irradiated L1210 cells (4500 rad) nor L1210 cell conditioned media suppressed erythroid colony formation. It is suggested that in L1210 leukemia erythropoiesis is decreased because of a cell-to-cell inhibitory action of the leukemia cells on CFU-E.
研究了L1210可移植白血病细胞对CD2F1小鼠骨髓祖细胞(CFU-E)体外形成红系集落的影响。采用甲基纤维素技术进行克隆细胞培养。人尿促红细胞生成素作为刺激物。孵育44小时后,八个或更多红系细胞的聚集体被计为集落。在6天前静脉注射5×10⁴个L1210细胞的小鼠骨髓细胞中可检测到的CFU-E数量远低于正常骨髓细胞。当将1.3×10⁵个白血病小鼠的骨髓细胞或L1210腹水细胞与等量的正常细胞一起培养时,相对于仅用正常细胞的对照,表达的CFU-E数量分别减少了51%和86%。无论是经4500拉德致死剂量照射的L1210细胞,还是L1210细胞条件培养基,均未抑制红系集落形成。提示在L1210白血病中,由于白血病细胞对CFU-E的细胞间抑制作用,红细胞生成减少。