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人骨髓间充质干细胞体外扩增的生物学评估 被引量:13

Biological Appraisal of Human Bone Marrow Mesenchymal Stem Cells During Ex-Vivo Expansion
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摘要 本研究旨在对骨髓间充质干细胞(mesenchymal stem cells,MSC)进行移植前增殖分化能力测定,病毒学检查,核型分析,PCR-STR和HLA的检测,以便为临床应用提供安全、可靠的移植细胞。采用贴壁法分离骨髓MSC,在相同条件下分别考察各代细胞形态、生长、表面标记、成骨、成脂分化能力的变化情况,并进行不同生长时期的核型分析,利用HLA-SBT技术检测4个不同供者来源的MSC的HLA-I和HLA-II位点的高分辨分型;应用PCR-STR技术检测4个不同供者来源的MSC基因遗传标记。并且利用ELISA方法检测HIV,HBV,HCV和TP,使用PCR方法检测支原体污染。结果表明:随着传代次数增加,MSC的增殖能力、成骨能力均有所下降。在扩增过程中,MSC始终保持较高的纯度,CD29、CD44、CD105、CD166、CD73均表达阳性,CD14、CD34、CD45、CD80和CD86均表达阴性。在8代以前未发现核型变异。4个不同供者来源的MSC的HLA高分辨分型和STR基因分型结果为MSC3的TP表达阳性,MSC2在5代出现支原体污染。结论:在体外培养过程中MSC干细胞特性逐渐丢失,其中向成骨方向的分化潜能降低。MSC在8代以前可作为实验研究及临床应用的良好对象。 This study was aimed to investigate the characteristics of human bone marrow mesenchymal stem cells during ex-vivo expansion, MSCs were isolated from human bone marrow. At each passage, the characteristics of proliferation kinetics, osteogenic and adipogenic differentiation potential were analyzed, and cell morphology, surface markers were investigated as well. The karyotype analysis was done in different passage cells. The infection HIV, HCV, HBV and TP were detected by ELISA. Mycoplasma contamination in vitro was detected by PCR method. HLA-SBT was used to reanalyze the results of HLA antigens and alleles. STR genetic loci were detected by PCR in the MSC1, MSC2, MSC3 and MSC4. The results indicated that the proliferative ability and osteogenic potential decreased with the increase of passage number during culture expansion. The multiple differentiation potential of MSCs was maintained during their life span. Karyotype analysis showed that MSCs from 4 groups before passsage 8 were normal. The expression of CD29, CD44, CD105, CD166 and CD73 were positive. The expression of CD14, CD34, CIM5, CD80, CD86 were all negative. SBT was used to identify HLA-A, B, Cw, DRB1 , DRPB1, DQ alleles in the MSC1, MSC2, MSC3, MSC4. The genetype of STR in the MSC1 ,MSC2 ,MSC3 ,MSC4 was different. MSC 3 was examined by TP-ELISA to confLrm the infectious disease of TP. MSC2 was contaminated by mycoplasma at passage 5. It is concluded that culture expansion causes MSCs to gradually lose their stem cell properties. During ex-vivo expansion of MSCs, the osteogenic differentiation potential is decreased. MSCs before passage 8 can be a valuable subject for basic research and clinical application.
出处 《中国实验血液学杂志》 CAS CSCD 2008年第3期639-644,共6页 Journal of Experimental Hematology
基金 广东省医学科学技术研究基金资助项目(编号GDWSTJJ342128197410280329) 广州市医药卫生项目资助项目(编号2006-YB-140)
关键词 骨髓间充质干细胞 成骨 成脂 STR HLA mesenchymal stem cell osteogenesis adipogenesis STR HLA
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参考文献8

  • 1Phinney DG, Prockop DJ. Concise review: mesenchymal stem/multipotent stromal cells : the state of transdifferentiation and modes of tissue repair-current views. Stem Cells, 2007 ; 25:2896 - 2902.
  • 2Le-Blanc K, Ringden O, Mesenchymal stem cells: properties and role in clinical bone marrow transplantation. Curt Opin Immunol, 2006 ; 18:586 - 591.
  • 3吴洁莹,廖灿,许遵鹏,陈劲松,辜少玲.人骨髓间充质干细胞分离鉴定方法的改进[J].中国实验血液学杂志,2006,14(3):557-560. 被引量:11
  • 4周征,姜尔烈,王玫,刘庆国,翟文静,黄勇,王荷花,韩明哲.成人骨髓间充质干细胞中各亚群的比较研究[J].中国实验血液学杂志,2005,13(1):54-58. 被引量:12
  • 5Bianco P, Riminucci M. Bone marrow stromal stem cells: nature, biology, and potential applications, Stem Cells, 2001 ; 19 : 180 - 192.
  • 6Cobo F, Stacey GN, Hunt C, et al. Microbiological control in stem cell banks: approaches to standardization.' Appl Microbiol Biotechnol, 2005 ; 68:456 -466.
  • 7Kristt D, Israeli M, Narinski R, et al. Hematopoietic chimerism monitoring based on STRs: quantitative platform performance on sequential samples. J Biomol Tech, 2005 ; 16:380 - 391.
  • 8Petersdorf EW. Immunogenomics of unrelated hematopoietic cell transplantation. Curt Opin Immunol. 2006 ; 18:559 - 564.

二级参考文献16

  • 1Pittenger MF, Meckay AM, Beck SC, et al. Multilineage potential of adult human mesenchymal stem cells. Science, 1999; 284:143- 147
  • 2Bruder SP, Jaiswal N, Haynesworth SE. Growth kinetics, self-renewal, and the osteogenic potential of purified human mesenchymal stem cells during extensive subcultivation and following cryopreservation. J Cell Biochem, 1997; 64:278-294
  • 3Colter DC, Class R, DiGirolamo CM, et al. Rapid expansion of recycling stem cells in cultures of plastic-adherent cells from human bone marrow. Proc Natl Acad Sci USA, 2000; 97:3213 -3218
  • 4Friedenstein AJ, Chailakhjan RK, Lalykina KS, et al. The development of fibroblast colonies in monolayer cultures of guinea-pig bone marrow and spleen cells. Cell Tissue Kinet, 1970; 3:393-403
  • 5Colter DC, Sekiya I, Prockop DJ, et al. Identification of a subpop ulation of rapidly self-renewing and multipotential adult stem cells in colonies of human marrow stromal cells. Proc Natl Acad Sci USA,2001; 98:7841-7845
  • 6Caplan AI.Mesenchymal stem cells.J Orthop Res,1991; 9:641-650
  • 7Devine SM,Hoffman R.Role of mesenchymal stem cells in hematopoietic stem cell transplantation.Curr Opin Hematol,2000; 7:358-363
  • 8Maitra B,Szekely E,Gjini K,et al.Human mesenchymal stem cells support unrelated donor hematopoietic stem cells and suppress T-cell activation.Bone Marrow Transplant,2004; 33:597-604
  • 9Le-Blanc K,Rasmusson I,Sundberg B,et al.Treatment of severe acute graft-versus-host disease with third party haploidentical mesenchymal stem cells.Lancet,2004; 363 (9419):1439-1441
  • 10Pittenger MF,Mackay AM,Beck SC,et al.Multilineage potential of adult human Mesenchymal stem cells.Science,1999; 284(5411):143-147

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