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作 者:师伟[1] 韩姝[1] 李艳华[1] 谢小燕[1] 施双双[1] 陈琳[1] 白慈贤[1] 闫舫[1] 南雪[1] 王韫芳[1] 裴雪涛[1]
机构地区:[1]军事医学科学院输血研究所干细胞与再生医学研究室,北京100850
出 处:《生物化学与生物物理进展》2005年第9期835-841,共7页Progress In Biochemistry and Biophysics
基 金:国家重点基础研究发展规划项目(973)(2001CB509906);国家高技术"863"计划重大专项资助项目(2002AA205051;2003AA205160).~~
摘 要:Wnt信号通路在造血干/祖细胞自我更新的过程中发挥至关重要的作用.纯化的Wnt3a蛋白可以实现造血干/祖细胞的扩增.通过病毒转染原代小鼠骨髓基质细胞,建立转基因滋养层细胞.通过共培养对转基因滋养层细胞扩增CD34+造血干/祖细胞的作用进行了研究.实验结果显示,与普通滋养层加细胞因子组相比,经转基因滋养层加细胞因子组培养的CD34+造血干/祖细胞集落形成能力(CFC)是其(1.55±0.06)倍;混合集落形成能力是其(1.95±0.26)倍;高增殖潜能集落形成能力(HPP-CFC)是其(1.45±0.40)倍;LTC-IC活性是其(3.83±0.86)倍.结果表明,转基因滋养层细胞通过分泌具有天然活性的Wnt3a蛋白能在体外有效地扩增造血干/祖细胞的数量.The Wnt signalling pathway plays an important role in regulation of haematopoietic stem cells (HSCs) self-renewal. Purified Wnt3a could remarkably enhance expansion of HSCs. A transgenic bone marrow stromal cells were established by using adenoviral vector mediated Wnt3a gene transfection. The effect of transgenic stromal cells as feeder layer on expansion of CD34^+ cells was studied. The group of Wnt3a transfected BM stromal cells with cytokines displays the best expansion effect on of human umbilical cord blood CD34^+ hematopoietic stern/progenitor cells in four groups. In vitro, expansion of CD34^+ cells, when cocultured with Wnt3a modified stromal cells in the presence of cytokines, was significantly enhanced: CFC by (1.55±0.06) fold; CFC (mix) by (1.95±0.26) fold; HPP-CFC by (1.45±0.40) fold; LTC-IC by (3.83±0.86) fold ,compared with nontransgenic stromal cells with cytokines group. These results strongly suggest that Wnt3a modified BM stromal cells may be a suitable feeder layer for expansion of haematopoietic stern/progenitor cells in vitro.
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