杨光,裴雪涛,李梁,周雅德,冯凯,白慈贤.TPO基因修饰的基质细胞对巨核系细胞的定向扩增作用[J].中华放射医学与防护杂志,2001,21(5):335-338
TPO基因修饰的基质细胞对巨核系细胞的定向扩增作用
Regulation of megakaryocytopoiesis by TPO gene-modified stromal cells
投稿时间:2000-11-10  
DOI:
中文关键词:  造血细胞  巨核系细胞  基质细胞  血小板生成素(TPO)
英文关键词:Hematopoietic cells  Megakaryocytic cells  Stromal cells Thrombopoietin(TPO)
基金项目:国家重点基础研究发展规划项目(973)(G1999053903);国家杰出青年科学基金资助项目(39825111)
作者单位
杨光 100580 军事医学科学院输血研究所 
裴雪涛 干细胞研究中心 
李梁 干细胞研究中心 
周雅德 重庆儿童医院 
冯凯 干细胞研究中心 
白慈贤 干细胞研究中心 
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中文摘要:
      目的 研究TPO基因修饰的基质细胞对CD34+造血细胞向巨核系细胞定向增殖分化的影响.方法 将TPOcDNA构建到pBabepura中,通过"乒乓转染法"获得产高滴度逆转录病毒载体的包装细胞;利用所获的病毒上清转染基质细胞HFCL,用Northernblot检测细胞中TPO基因的表达,并利用TPO依赖株检测上清中的TPO活性;以未转基因的HFCL为对照,将CD34+造血细胞在TPO基因修饰的HFCL支持下扩增,用流式细胞仪检测扩增细胞中表型为CD34+CD41+和表型为CD41+CD61+细胞的比例.结果 基质细胞HFCL能够有效表达外源性TPO基因,在HFCLTPO培养上清中有075ngml水平的TPO活性;并且在HFCLTPO支持下,CD34+造血细胞经过7d扩增后,CD34+CD41+细胞的比例为(137±20)%,HFCL为(65±18)%(P<001);CD41+CD61+细胞的比例为(119±07)%,略高于HFCL的(106±15)%(P>005).结论 基质细胞能够有效表达外源性TPO基因和其蛋白,而且TPO基因修饰的基质细胞能显著促进CD34+CD41+巨核祖细胞的扩增,但对较成熟的CD41+CD61+巨核细胞影响不明显.
英文摘要:
      Objective To study the effect of TPOgene-modified stromal cells on stimulating megakaryocytopoiesis. Methods Retroviral vectors carrying TPOgene were constructed and used to transfect the stromal cell line HFCL by using a "Ping-pang" technique.The expression of TPOgene was detected by Northern blot and dependent cell line TD-3.By contrast with expansions supported by non-modified stromal cells,CD34+ hematopoietic cells from cord blood were expanded on gene-modified stromal cells for 7 days.Finally,percentages of CD34 +CD41+ cells and CD41+CD61+ cells were analyzed by flow cytometry. Results The stromal cell line HFCLcould express the TPOgene transduced by using the retroviral vectors,and the activity of TPO in supernatant of the tranduced HFCLcells was 075 ng/ml.The percentages of CD34+CD41+ megakaryocyte-committed progenitors in the presence of TPO gene-modified HFCL cells(137%±20%) were higher than those in the nontransduced HFCL cells (65%±18%),and there was no difference statistically on the percentages of the CD41+CD61+ cells between the cultures supported by transduced and non-tranduced stromal cells. Conclusion Stromal cell line HFCL could express the TPOwith biological activities after transfected by retroviral vectors,and enhance the growth of CD34+CD41+ megakaryocyte-committed progenitor cells.
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