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脐血造血细胞中AC_(133)抗原表达及其功能特征研究 被引量:1

The expression and functional characteristics of AC_(133)antigen in cord blood hematopoietic cells
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摘要 目的 探讨AC133抗原在正常人造血细胞中表达的意义。方法 采用双色直接免疫荧光标记法 ,使用流式细胞仪测定脐血中造血细胞的免疫表型。通过祖细胞集落形成单位 (CFC)和长期培养启动细胞 (LTC IC)的测定对脐血中AC+ 133、CD+ 34 和AC-133CD+ 34 细胞的造血潜能进行了研究。结果 脐血单个核细胞 (MNCs)中AC+ 133细胞比例为 0 67% ,AC+ 133细胞中 93 4%表达CD34 抗原 ,94 2 %为PKH2 6 阳性。虽然三群细胞产生的CFC总数差异无显著性 ,但AC+ 133细胞中 5 0 %以上为粒 单集落形成单位 ,CD+ 34 、AC-133CD+ 34 细胞中 60 %和 80 %以上为红系集落形成单位。AC+ 133细胞产生的LTC IC显著高于CD+ 34 和AC-133CD+ 34 细胞。体外培养 7d ,AC+ 133细胞组细胞总数和CFC分别扩增 2 8 2和 7 1倍 ,6 8%细胞仍保持PKH2 6阳性。结论 脐血中早期造血干 /祖细胞富集在AC+ 133细胞群中 ,AC+ 133细胞在体外具有较强的增殖能力 ,既能产生大量的早期定向祖细胞 ,又能保持一定数量的早期干 /祖细胞 ,AC133抗原可作为临床分选造血干 Objective To explore the significance of AC 133 antigen expression on cord blood (CB) hematopoietic cellls Methods The immunophenotype of CB hematopoietic cells was analyzed by flow cytometric two color direct immunoflurescence method Hematopoietic activity of AC + 133 , CD + 34 and AC - 133 CD + 34 cells in CB was examined by analyzing clonogenic capacity, number of LTC IC and ex vivo expansion ability Results AC + 133 cells consisted of 0 67% of the total CB MNCs Of the AC + 133 cells, 93 4% expressed CD 34 antigen and 94 2% was PKH + 26 ? Although the total number of CFC was the same in the AC - 133 CD + 34 fraction as in the CD + 34 and AC - 133 fractions, the number of LTC IC was much higher in the AC + 133 fraction In addition, the features of the colonies grown from these three fractions were quite different Approximately 50% of the colonies derived from the AC + 133 fraction were CFU GM, whereas more than 60% of the colonies derived from the CD + 34 fraction and 80% of the colonies derived from the AC - 133 CD + 34 fraction were BFU E After 7 d ex vivo expansion, the total number of cells and CFC increased 28 2 fold and 7 1 fold respectively in AC + 133 cell populations, 6 8% of the cells was PKH + 26 . Conclusions These findings suggest that the early stem/progenitor cells of CB are enriched in AC + 133 fraction, AC + 133 cells contain higher proliferative efficiency during ex vivo culture It can generate either committed progenitors or early stem/progenitors AC 133 antigen would be a useful marker for clinical selection of hematopoietic stem/progenitors
出处 《中华内科杂志》 CAS CSCD 北大核心 2002年第12期798-800,共3页 Chinese Journal of Internal Medicine
基金 国家自然科学基金资助项目 (3992 80 10 ) 海外青年学者合作研究基金资助项目
关键词 脐血 造血干细胞 免疫表型分型 AC133抗原 双色直接免疫荧光标记法 Fetal blood Hematopoietic stem cells Immunophenotying AC 133 antigen
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参考文献6

  • 1Yin AH,Miraglia S,Zanjani ED,et al.AC133, a novel marker for human hematopoietic stem and progenitor cells[].Blood.1997
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同被引文献11

  • 1Kanamaru S, Kawano Y, Watanabe T, et al. Low numbers of megakaryocyte progenitors in grafts of cord blood cells may result in delayed platelet recovery after cord blood cell transplant. Stem Cells, 2000;18:190 - 195.
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  • 3Bruno S, Gunetti M, Gammaitoni L, et al. Fast but durable megakaryocyte repopulation and platelet production in NOD/SCID mice transplanted with ex-vivo expanded human cord blood CD34^+ cells. Stem Cells, 2004 ;22 : 135 - 143.
  • 4Drayer AL, Smit Sibinga CT, Esselink MT, et al. In vitro megakaryocyte expansion in patients with delayed platelet engraftment ,after autologous stem cell transplantation. Ann Hematol, 2002;81:192 - 197.
  • 5Yao CL, Feng YH, Lin XZ, et al. Characterization of serum-free ex vivo-expanded hematopoietic stem cells derived from human umbilical cord blood CD133 ( + ) cells. Stem Cells Dev, 2006; 15 : 70 - 78.
  • 6De-Wynter EA, Buck D, Hart C, et al. CD34^+ AC133^+ cells isolated from cord blood are highly enriched in long-term cultureinitiating cells, NOD/SCID-repopulating cells and dentritic cell progenitors. Stem Cells, 1998 ; 16:387 - 396.
  • 7De Bruyn C, Delforge A, Martiat P, et al. Ex vivo expansion of megakaryocyte progenitor cells: cord blood versus mobilized peripheral blood. Stem Cells Dev, 2005 ; 14:415 -424.
  • 8Charrier S, Boiret N, Fouassier M, et al. Normal human bone marrow CD34( + ) CD133( + ) cells contain primitive cells able to produce different categories of colonyforming unit megakaryocytes in vitro. Exp Hematol, 2002; 30:1051 - 1060.
  • 9Shaw PH, Olszewski M, Kletzel M. Expansion of megakaryocyte precursors and stem cells from umbilical cord blood CD346+ cells in collagen and liquid culture media. J Hematother Stem Cell Res, 2001 ;10:391 -403.
  • 10郝思国,孙关林,邬维礼,吴英理.人脐血CD133^+细胞体外短期培养中生物学特性的变化[J].中国实验血液学杂志,2003,11(6):569-575. 被引量:9

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