期刊文献+

人参多糖对移植性人白血病模型小鼠作用观察 被引量:1

Effect of Ginseng polysaccharide on human leukemia SCID mouse model
下载PDF
导出
摘要 目的建立重度联合免疫缺陷(SCID)小鼠人白血病模型,观察人参多糖在体内对白血病细胞的药理学作用.方法在SCID小鼠尾静脉分别接种K562细胞建立SCID小鼠人白血病模型,应用组织细胞化学、RT-PCR、流式细胞术、组织病理监测在给予人参多糖前后白血病模型SCID小鼠的外周血、骨髓、肝、脾中的白血病细胞.结果 SCID小鼠人白血病模型外周血象在疾病早期无明显变化,第18天白细胞数略有升高,光镜下可检测到1%~4%人白血病细胞,病程后期,白细胞明显增高,血涂片检查人白血病细胞占10%;经GPS注射后,SCID小鼠一般状况明显好于对照组,其肺、肾等脏器的炎症及病理变化减轻.结论人参多糖在体内能有效地治疗髓系白血病,且未发现有明显的毒副作用. Objective To establish the human leukemia model in the severe combined immunodeficiency (SCID) mice and to investigate the pharmacological action of Ginseng polysaccharide (GPS) on leukemic cells in vivo. Methods The human leukemia mouse model was established by implanting K562 cells into the caudal vein of SCID mouse. Histochemistry, RT-PCR, flow cytometry, histopathology were used to monitor the leukemic cells in peripheral blood, bone marrow, liver, spleen of leukemia SCID mouse models, before and after injection of GPS. The mice receiving the physiological saline instead of GPS served as controls. Results The peripheral blood cells did not change so much in SCID mice in the earlier period of leukemia, the total number of WBC slightly increased and promyelocytes of leukemia could be detected 1% -4% on day 18 after K562 cells implantation. In last phase of leukemia, WBC significantly rose and could be monitored 10%. After injection of GPS, the common condition of mouse models was more improved than that of controls, the inflammation and pathological changes of organs ameliorated. Conclusion GPS can effectively suppress leukemia in vivo and is found no obvious ill effect.
出处 《第三军医大学学报》 CAS CSCD 北大核心 2006年第7期677-680,共4页 Journal of Third Military Medical University
基金 国家自然科学基金资助项目(39670880)~~
关键词 人参多糖 K562 白血病动物模型 Ginseng polysaccharide K562 severe combined immunodeficiency animal model
  • 相关文献

参考文献10

二级参考文献21

  • 1王亚平,祝彼得.当归多糖对小鼠粒单系血细胞发生的影响[J].解剖学杂志,1993,16(2):125-129. 被引量:22
  • 2Rath A V, Schmahl G E, Niemeyer C M. Expression of transcription factors during sodium phenylacetate induced erythroid differentiation in K562 cells[J]. Blood Cells Mol Dis, 1997, 23(2): 27-38.
  • 3Aoki S, Kong D, Matsui K, et al. Smenospongine, a spongean sesquiterpene aminoquinone, induces erythroid differentiation in K562 cells[J]. Anticancer Drugs, 2004, 15(4): 363-369.
  • 4Bosma GC,Custer RP,Bosma MJ.A severe combined immunodeficiency mutation in the mouse[].Nature.1983
  • 5Dazzi F,Capelli D,Hasserjian R,et al.The kinetics and extent of engraftment of chronic myelogenous leukemia cells in non-obese diabetic severe combined immunodeficiency mice reflect the phase of the donor′s disease: an in vivo model of chronic myelogenous leukemia biology[].Blood.1998
  • 6McCune JM,Namikawa R,Kaneshima H,et al.The SCID-mouse: murine model for the analysis of human hematolymphoid differentiation and function[].Science.1988
  • 7Wang JC,Lapidot T,Cashman JD,et al.High level engraftment of NOD SCID mice by primitive normal and leukemic hematopoietic cells from patients with chronic myeloid leukemia in chronic phase[].Blood.1998
  • 8Petzer AL,Eaves CJ,Lansdorp PM,et al.Characterization of primitive subpopulations of normal and leukemic cells present in the blood of patients with newly diagnosed as well as established chronic myeloid leukemia[].Blood.1996
  • 9O′Brien S,Jeha S,Kantarjian H,et al.Engraftment of chronic prolymphocytic and T cell leukemia in SCID mice[].Leukemia.1996
  • 10Hall PD,Willingham MC,Kreitman RJ,et al.DT388-GM-CSF, a novel fusion toxin consisting of a truncated diphtheria toxin fused to human granulocyte-macrophage colony-stimulating factor, prolongs host survival in a SCID mouse model of acute myeloid leuke-mia[].Leukemia.1999

共引文献61

同被引文献31

  • 1赵洁,黄卫国,宋颖,何洁,谭辉,苏琦.急性早幼粒白血病HL-60细胞动物模型的建立与鉴定[J].南华大学学报(医学版),2005,33(2):181-183. 被引量:5
  • 2Bosma GC,Custer RP,Bosma MJ.A severe combined immunodeficiency mutation in the mouse[J].Nature,1983,301(5900):527-30.
  • 3Mosier DE,Stell KL,Gulizia RJ,et al.Homozvgous acid/acid;beige/beige mice have low levels of spontaneous or neonatal T cell-induced B cell generation[J].J Exp Med,1993,177(1):191-4.
  • 4Prochazka M,Gaskins HR,Shultz LD.The nonobese diabetic SCID mouse model for spontaneous thymom agenesis associated with immunodeficiency[J].Proc Natl Acad Sci USA,1992,89(8):3290-4.
  • 5Feuring-Buske M,Gerhard B,Cashman J,et al.Improved engraftment of human acute myeloid leukemia progenitor cells in beta2-microglobulin-deficient NOD/SCID mice and in NOD/SCID mice transgenic for human growth factors[J].Leukemia,2003,17(4):760-3.
  • 6Kolet O,Peled A,Byk T,et al.β2 microglobulin deficient(β2mnul1)NOD/SCID mice are excellent recipients for studying human stem cell function[J].Blood,2000,95(10):3102-5.
  • 7Ito M,Hiramatsu H,Kobayashi K,et al.NOD/SCID/γcnullmouse:an excellent recipient mousemodel for engraftment of human cells[J].Blood,2002,100(9):3175-82.
  • 8Agliano A,Martin-Padura I,Mancuso P,et al.Human acute leukemia cells injected in NOD/LtSz-scid/IL-2Rγnull mice generate a faster and more efficient disease compared to other NOD/scid-related strains[J].Int J Cancer,2008,123(9):2222-7.
  • 9Zimmerman B,Niewiesk S,Lairmore MD,et al.Mouse Models of Human T Lymphotropic Virus Type-1-Associated Adult T-Cell Leukemia/Lymphoma[J].Vet Pathol,2010,47(4):677-89.
  • 10Nakamura Y,Ito M,Yanamoto T,et al.Engraftment of NOD/SCID/γcnull mice with multilineage neoplastic cells from patients with juvenile myelomonocytic leukaemia[J].British Journal of Haematology,2005,130(1):51-7.

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