期刊文献+

热变性对血细胞流式细胞术分析结果的影响 被引量:1

Effect of Heat Denaturation on Blood Cells Analyzed by Flow Cytometry
下载PDF
导出
摘要 目的初步探讨热变性对外周血细胞在流式细胞术分析结果中的影响,从而提高流式-荧光原位杂交(Flow-FISH)技术的应用。方法收集5例非骨髓造血干细胞疾病患者肝素抗凝外周血标本,以CD45-Alexa Fluor647标记细胞表面抗原,高温变性后,采用流式细胞术分析热变性前后外周血有核细胞的散射光信号和荧光信号变化。结果热变性后,外周血粒细胞的侧向散射光明显缩小;单核细胞不易通过散射光被区分和设门。所有细胞CD45表达强度均减弱,以淋巴细胞为著;通过侧向散射光和CD45设门虽能大致区分各群细胞,但不及未热变性细胞清晰。结论热变性后,外周血细胞在流式细胞术中的散射光信号和荧光信号均发生了变化,按照常规FSC/SSC和CD45/SSC方法设门进行细胞亚群分析的结果不精确,利用系列特异性荧光抗体标记是一种有前景的方法。 Objective To investigate the effect of heat denaturation on peripheral blood cells analyzed by flow cytometry and to improve the application of Flow cytometry-Fluorescence in situ hybridization (Flow-FISH).Methods Heparinized peripheral blood were sampled from 5 patients without hematopoietic stem cell disease,isolated nucleated cells were labeled with CD45-Alexa Fluor (R) 647,then denatured by high temperature.The scatter signals and fluorescence signals were analyzed by flow cytometry,on cells with and without heat denaturation separately.Results After heat denaturation,the sideward light scatter of granulocytes became markedly smaller,and the monocytes were difficult to be gated.CD45 expression of all cells became weaker,especially the lymphocytes; and cell subgroups could be differentiated by CD45 and sideward light scatter,while it was not as clear as cells without heat denaturation.Conclusion Heat denaturation could change both light scatter signal and fluorescence intensity by flow cytometry,and the routine method to gate cell groups might be not precise.Therefore,fluorescence labeled lineage specific antibody may be useful method to apply in Flow-FISH.
出处 《标记免疫分析与临床》 CAS 2014年第3期290-293,共4页 Labeled Immunoassays and Clinical Medicine
基金 国家自然科学基金资助项目(编号81000200) 北京市卫生系统高层次卫生技术人才培养项目(编号2011-3-092) 首都医科大学基础临床合作研究基金(编号12JL28)
关键词 热变性 流式细胞术 散射光 CD45 Heat denaturation Flow cytometry Light scatter CD45
  • 相关文献

参考文献10

  • 1Baerlocher G M, Mak J, Tien T, et al. Telomere length measurement by fluorescence m situ hybridization and flow eytometry: tips and pitfalls. Cytometry, 2002, 47(2) : 89-99.
  • 2Spyridopopulos I, Erben Y, Brummendorf T H, et al. Telomere gap between granulocytes and lymphocytes is a determinant for hematopoietic progenitor cell impailrnent in patients with previous myocardial infarction. Arterioscler Thromb Vasc Bial, 2008, 28 (5) : 968-974.
  • 3刘博,崔巍,韩冰,汪玄,林洁,赵永强.流式-原位杂交方法在中国骨髓衰竭综合征患者端粒长度检测中的应用[J].中国医学科学院学报,2009,31(5):547-550. 被引量:5
  • 4Elena C, Rumi E, Portolan M, et al. Flow-FISH evaluation of telomere length in Philadelphia- negative myeloproliferative neoplasms. Haematologica, 2011,96(7) : 1236-1238.
  • 5Schmid I,Dagarag M D, Hausner M A, et al. Simultaneous flow cytometric analysis of two cell surface markers, telomere length, and DNA content. Cytometry, 2002,49 ( 3 ) : 96-105.
  • 6Baerlocher G M,Vulto I, Jong D, et al. Flow cytometry and FISH to measure the average length of telomeres ( flow FISH ). Nature Protocols,2006, 1 ( 5 ) : 2365-2376.
  • 7Rollison D E, Epling-Bumette P K, Park J Y, et al. Telomere length in myelodysplastic syndromes. Leukemia & Lymphoma, 2011,52(8) : 1528-1536.
  • 8Biegler K A,Anderson A K , Wenzel L B, et al. Longitudinal change in telomere length and the chronic stress response in a randomized pilot biobehavioral clinical study: implications for cancer prevention. Cancer Prey Res(Phila) ,2012, 5(10) : 1173-1182.
  • 9郭天姣,孙婉玲,张维,马晓彩,刘聪艳,贺景娟,徐娟.流式-荧光原位杂交技术在骨髓增生异常综合征患者骨髓CD34^+细胞相对端粒长度检测中的应用[J].中国实验血液学杂志,2013,21(5):1195-1199. 被引量:4
  • 10Rufer N, Brummendorf T H, Kolvraa S, et al. Telomere fluorescence measurements in granulocytes and T lymphocyte subsets point to a high turnover of hematopoietic stem cells and memory T cells in early childhood. J Exp Med, 1999,190(2) : 157-167.

二级参考文献17

  • 1Swerdlow SH,Campo E,Harris NL,et al.WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues.4th Edition,Lyon:IARC,2008:88-107.
  • 2Mittelman M,Oster HS,Hoffman M,et al.The lower risk MDS patient at risk of rapid progression.Leuk Res,2010; 34(12):1551-1555.
  • 3Greenwood M J,Lansdorp PM.Telomeres,telomerase,and hematopoietic stem cell biology.Arch Med Res,2003; 34(6):489-495.
  • 4Blasco MA.Telomere length,stem cells and aging.Nat Chem Biol,2007; 3(10):640-649.
  • 5Ohyashiki JH,Iwama H,Yahata N,et al.Telomere stability is frequently impaired in high-risk groups of patients with myelodysplastic syndromes,Clin Cancer Res,1999; 5(5):1155-1160.
  • 6Sieglova Z,Zilovcova S,Cermak J,et al.Dynamics of telomere erosion and its association with genome instability in myelodysplastic syndromes (MDS) and acute myelogenous leukemia arising from MDS:a marker of disease prognosis? Leuk Res,2004; 28(10):1013-1021.
  • 7Goehring G,Lange K,Hofmann W,et al.Telomere shortening,clonal evolution and disease progression in myelodysplastic syndrome patients with 5q deletion treated with lenalidomide.Leukemia,2012; 26(2):356-358.
  • 8Chakraborty S,Sun CL,Francisco L,et al.Accelerated telomere shortening precedes development of therapy-related myelodysplasia or acute myelogenous leukemia after autologous transplantation for lymphoma.J Clin Oncol,2009; 27(5):791-798.
  • 9Baerlocher GM,Mak J,Tien T,et al.Telomere length measurement by fluorescence in situ hybridization and flow cytometry:tips and pitfalls.Cytometry,2002 ; 47 (2):89-99.
  • 10Schmid I,Dagarag MD,Hausner MA,et al.Simultaneous flow cytometric analysis of two cell surface markers,telomere length,and DNA content.Cytometry,2002 ; 49 (3):96-105.

共引文献5

同被引文献8

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