Sudo Y, Shimazaki C, Ashihara E, Kikuta T, Hirai H, Sumikuma T, Yamagata N, Goto H, Inaba T, Fujita N, Nakagawa M
Second Department of Medicine, Kyoto Prefectural University of Medicine, Kamigyoku, Japan.
Blood. 1997 May 1;89(9):3186-91.
We have previously shown that FLT-3 ligand (FL) mobilizes murine hematopoietic primitive and committed progenitor cells into blood dose-dependently. Whether FL also acts synergistically with granulocyte colony-stimulating factor (G-CSF) to induce such mobilization has now been investigated. Five- to 6-week-old C57BL/6J mice were injected subcutaneously with recombinant human G-CSF (250 microg/kg), Chinese hamster ovarian cell-derived FL (20 microg/kg), or both cytokines daily for 5 days. The number of colony-forming cells (CFCs) in peripheral blood increased approximately 2-, 21-, or 480-fold after administration of FL, G-CSF, or the two cytokines together, respectively, for 5 days. The number of CFCs in bone marrow decreased after 3 days but was increased approximately twofold after 5 days of treatment with G-CSF. The number of CFCs in the bone marrow of mice treated with both FL and G-CSF showed a 3.4-fold increase after 3 days and subsequently decreased to below control values. The number of CFCs in spleen was increased 24.2- and 93.7-fold after 5 days of treatment with G-CSF alone or in combination with FL, respectively. The number of colony-forming unit-spleen (CFU-S) (day 12) in peripheral blood was increased 13.2-fold by G-CSF alone and 182-fold by G-CSF and FL used together after 5 days of treatment. Finally, the number of preCFU-S mobilized into peripheral blood was also increased by the administration of FL and G-CSF. These observations show that FL synergistically enhances the G-CSF-induced mobilization of hematopoietic stem cells and progenitor cells into blood in mice, and that this combination of growth factors may prove useful for obtaining such cells in humans for transplantation.
我们先前已表明,FMS样酪氨酸激酶3配体(FL)能剂量依赖性地将小鼠造血原始祖细胞和定向祖细胞动员到血液中。现在已经研究了FL是否也与粒细胞集落刺激因子(G-CSF)协同作用以诱导这种动员。对5至6周龄的C57BL/6J小鼠皮下注射重组人G-CSF(250微克/千克)、中国仓鼠卵巢细胞衍生的FL(20微克/千克),或两种细胞因子,每日注射,共5天。分别给予FL、G-CSF或两种细胞因子5天后,外周血中集落形成细胞(CFC)的数量分别增加了约2倍、21倍或480倍。骨髓中CFC的数量在3天后减少,但在用G-CSF治疗5天后增加了约两倍。用FL和G-CSF联合治疗的小鼠骨髓中CFC的数量在3天后增加了3.4倍,随后降至对照值以下。单独用G-CSF或与FL联合治疗5天后,脾脏中CFC的数量分别增加了24.2倍和93.7倍。治疗5天后,单独使用G-CSF可使外周血中脾集落形成单位(CFU-S)(第12天)的数量增加13.2倍,G-CSF和FL联合使用可使其增加182倍。最后,给予FL和G-CSF也增加了动员到外周血中的前CFU-S的数量。这些观察结果表明,FL协同增强了G-CSF诱导的小鼠造血干细胞和祖细胞向血液中的动员,并且这种生长因子的组合可能被证明对在人类中获取此类细胞用于移植是有用的。