期刊文献+

多发性硬化患者造血干/祖细胞及其亚群富集纯化的研究 被引量:1

Collection and purification of CD34^+ hematopoietic stem (progenitor) cells and its sub-groups from patients with multiple sclerosis
下载PDF
导出
摘要 目的 :获得高纯度造血干 /祖细胞 (HSC/HPC)及其亚群 ,用于多发性硬化 (MS)造血干细胞移植治疗和生物学特性的研究 .方法 :用免疫磁珠法 (MiniMACS)从MS患者骨髓中富集CD34+ 细胞后再用荧光激活细胞分选 (fluorescentacti vatedcellsorter,FACS)纯化CD34+ /CD38+ 和CD34+ /CD38-细胞亚群 .结果 :MiniMACS分选的CD34+ 细胞群纯度达 91 % ,FACS分选的CD34+ /CD38-和CD34+ /CD38+ 两细胞亚群纯度可达 98%以上 .结论 :MiniMACS和FACS两者结合可迅速大量纯化HSC/HPC及其重要细胞亚群 ,可用于临床MS造血干细胞移植。 AIM: To collect and purify the bone marrow CD34 + hematopoietic stem cells and its sub groups from the patients with multiple sclerosis. METHODS: CD34 + cells were collected and purified by means of imunomagnetic beads on MiniMACS device. Flow cytometry was emplyed to determine percentage of CD34 + cells, CD34 +/CD38 - cells and CD34 +/CD38 + cells before and after miniMACS. RESULTS: The purity of CD34 + cells amounted to more than 91% after the purification. The purity of CD34 +/CD38 - cells and CD34 +/CD38 + cells amounted to more than 98% after fluorescent activated cell sorter (FACS). CONCLUSION: The combination of MiniMACS and FACS can sort effectively the bone marrow CD34 + cells and its sub groups so that they may be used for hematopoietic stem cell transplantation, gene therapy and biological study of hematopoietic stem cells/hematopoietic progenitor cells (HSC/HPC) and its sub groups.
出处 《第四军医大学学报》 北大核心 2004年第3期233-235,共3页 Journal of the Fourth Military Medical University
基金 广西自然科学基金 (桂科基 0 342 0 0 8 1 )
关键词 造血干细胞 免疫磁珠法 流式细胞计量术 多发性硬化 hematopoietic stem cells MiniMACS flow ytometry multiple sclerosis
  • 相关文献

参考文献9

  • 1[1]Poser CM. Notes on the pathogenesis of multiple sclerosis [J]. Clin Neurosci, 1994;2(3-4):258-265.
  • 2[2]Fassas A, Anagnostopoulos A, Kazis A, et al. Peripheral blood stem cell transplantation in the treatment of progressive multiple sclerosis: First results of a pilot study [J]. Bone Marrow Fransplant, 1997;20(8):631-638.
  • 3[4]Ikehara S, Ohtisuki H, Good RA, et al. Prevention of type 1diabetes in monlbesediabetes nice by allogeneic bone marrow transplantation [J]. Proc Natl Acad Sci USA, 1985;82:7743.
  • 4[5]Tyndall A, Gratwohl A. Haemopoietic stem and progenitor cells in the treatment of severe autoimmune diseases [J]. Ann Rheum Dis, 1996;55:149.
  • 5[6]Ikehara S. Bone marrow transplantation for autoimmune diseases [J]. Acta Haematol, 1998;99:116-132.
  • 6[7]Krause D, Fackler M, Civin C, et al. CD34+: Structure, biology and clinical utility [J]. Blood, 1996; 87(1):1-13.
  • 7[8]Terstappen LWMM, Huang S, Safford M, et al. Sequential generation of hematopoietic colonies derive from single nonlineage committed CD34+/CD38- progenitor cells [J]. Blood, 1991; 77: 1218-1227.
  • 8[9]Huang S, Terstappen L. Lymphoid and myeloid differentiatiom of single human CD34+, HLA-DR+,CD34-, hematopoietic stem cells [J]. Blood, 1994; 83:1515-1525.
  • 9[10]Waller E, Olweus J, Lund-Johansen F, et al. The "common stem cell" hypothesis reevaluated: Human fetal bone marrow contains separate population of hematopoietic and stromal progenitors [J]. Blood, 1995; 85:2422-2435.

同被引文献2

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部