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作 者:张毅[1,2,3,4] 朱剑昆[1,2,3,4] 张雁云[1,2,3,4] 刘继明 邱玉华[1,2,3,4] 李新燕 刘蓓岭[1,2,3,4] 谢炜 郑列琳[1,2,3,4] 冯丽瑾 郭玲[1,2,3,4] 朱学东 强亦忠[1,2,3,4] 张学光
机构地区:[1]苏州医学院免疫研究室 [2]苏州医学院生物化学教研室 [3]苏州市第二人民医院检验科 [4]苏州医学院放射医学研究所
出 处:《中华血液学杂志》1998年第12期642-645,共4页Chinese Journal of Hematology
基 金:江苏省科委优秀青年教师基金;国防科工委基金
摘 要:目的:研究重组人白细胞介素8(rhIL8)动员小鼠造血干/祖细胞的生物学效应。方法:将rhIL8单独或联合重组人粒细胞集落刺激因子(rhGCSF)给BALB/c小鼠静脉内注射,观察BALB/c小鼠外周血单个核细胞(PBMNC)的增殖能力;并将PBMNC回输给经致死性照射(7.5Gy60Coγ射线照射)的BALB/c小鼠,观察其造血重建功能。结果:每只小鼠单独注射rhIL830μg15分钟后,外周血中混合细胞集落形成单位(CFUMix)数量达峰值[(194±61)×103/L],比对照组[(7±3)×103/L]明显升高;外周血中ckit+Sca1+细胞为(3186±517)×103/L,亦比对照组[(644±341)×103/L]明显升高;联合注射rhGCSF则可使外周血CFUMix和ckit+Sca1+细胞分别增高至(790±48)×103/L和(10729±2339)×103/L。单独注射rhIL8后动员的PBMNC回输给致死性照射的BALB/c小鼠,其外周血中骨髓造血重建活性(MRA)细胞比对照组明显升高,联合rhGCSF组外周血中MRA细胞数可达(356.3±87.7)×1?Objective: To study the mobilization effects of recombinant human IL 8(rhIL 8) on mouse peripheral blood hematopoietic progenitors (HPCs). Methods:A daily single dose of rhIL 8 was intravenously injected into normal or G CSF treated mice for two days. The number of colony forming unit Mix (CFU Mix) in peripheral blood was analyzed by colony assay, while the number of c kit +Sca 1 + HPCs was examined by immunofluorescence staining. In addition, colony forming unit of spleen (CFU S) and marrow repopulating ability (MRA) cells were examined by transplanting lethally irradiated mice. Results: Single dose of rhIL 8 (30μg) significantly increased the numbers of CFU Mix[(194±61)×10 3/L] and c kit + Sca 1 + cells [(3186±517)×10 3/L] in the peripheral blood as compared with that of normal saline controls [(7±3)×10 3/L and (644±341)×10 3/L] at 15 minutes after intravenous injection. G CSF could also increase peripheral CFU Mix and c kit + Sca 1 + cells to (790±48)×10 3/L and (10729±2339)×10 3/L, respectively, after subcutaneously injection for two days, this increase was further augmented by rhIL 8 injection. IL 8 alone or in combination with G CSF could significantly increase the number of CFU S and MRA cells in circulating blood. Conclusion: IL 8 alone or in combination with G CSF could significantly mobilize circulating HPCs.
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