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作 者:马东初[1] 孙英慧[2] 常奎忠[2] 戴兵[2] 刘亚革[2] 孙忱[1] 贾卫[1] 菅金龙[1] 金伯泉[1]
机构地区:[1]第四军医大学免疫学教研室,陕西西安710032 [2]沈阳军区总医院医学实验科,辽宁沈阳110016
出 处:《细胞与分子免疫学杂志》2001年第4期307-309,共3页Chinese Journal of Cellular and Molecular Immunology
基 金:国家自然科学基金资助;No. 30030130和No.39800072
摘 要:目的研究CD226在造血干/祖细胞上的表达分布。TPO诱导胎肝造血干/祖细胞增殖分化过程中,CD226表达的变化及可能的信号调控途径。方法采用鸡尾酒单抗阴性分离富集Lin-造血干/祖细胞,培养于含TPO的无血清培养体系中,用PD98059阻断MAPK信号转导途径,流式细胞仪双荧光分析CD226、CD34、CD41a和CD61的表达。结果CD226在Lin-CD34+细胞和Lin-CD34-细胞上均有表达。TPO可诱导Lin-CD41a-CD226-细胞先分化为CD41a+CD226-细胞,再进一步分化为CD41a+CD226+细胞,TPO也可诱导Lin-CD226+细胞表达CD41a和CD61。在培养的早期,PD98059可抑制CD34+CD226+细胞的减少,在晚期则可抑制CD41a+CD226+细胞的增多。结论CD226与造血干/祖细胞和巨核细胞的增殖分化可能具有密切的关系。Aim To investigate the expression of CD226 on Lin-hematopoietic stem/progenitor cells and TPO-induced Lin-cells as well as possible pathway of signal transduction for regulating expression of CD226 by TPO. Methods Lin-hematopoietic stem/progenitor cells isolated from fetal liver mononuclear cells by negative selection with human progenitor enrichment-antibodies cocktail including anti-CD2, -CD3, -CD14, -CD16, -CD19, -CD24, -CD56, -CD66b mAbs and glycophorin A mAb were incubated in serum-free IMDM supplemented with 15%of mixture of BSA, insulin, transferrin (BIT9500) and 100μg/L TPO for 18 days. In some experiments, PD98059, a MEK1 inhibitor, was added at a concentration of 20μmol/L. The expressions of CD226, CD34, CD41a and CD61 were analyzed by using flow cytometry with double-labelling technique. Results CD226 was expressed on both Lin-CD34+cells and Lin-CD34-cells. TPO firstly induced Lin-CD41a-CD226-cells to differentiate into CD226-CD41a+/CD61+cells and then into CD226+CD41a+/CD61+cells. TPO could also induce Lin-CD226+cells to express CD41a/CD61. PD98095 could suppress decrease in CD34+CD226+cells in the early period of the Lin-cell culture and inhibit increment in CD41a+CD226+cells in the later period. Conclusion CD226 seems to have a close relation with proliferation and differentiation of hematopoietic stem/progenitor cells and megakaryocytic progenitor cells.
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