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环孢素A对Th1细胞转录因子T-bet的影响

Effect of cyclosporine A on transcription factor T-bet of T helper 1 type cells
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摘要 目的研究环孢素A(CsA)对小鼠骨髓型正常巨噬细胞株Ana-1诱导Th1细胞转录因子T-bet的影响,探讨CsA在再生障碍性贫血(再障)治疗中的免疫抑制作用。方法①反转录聚合酶链反应(RT-PCR)方法检测Ana-1细胞株培养上清作用后正常小鼠外周血单个核细胞(PBMC)T-betmRNA的表达。②RT-PCR方法检测Ana-1细胞株培养上清加CsA作用后正常小鼠PBMCT-betmRNA的表达。结果①加入Ana-1细胞株培养上清后,T-betmRNA的表达水平为1.54±0.03,较对照组(1.03±0.06)增多(P<0.05);②加入Ana-1细胞株培养上清和CsA后,T-betmRNA的表达为0.66±0.02,较加入Ana-1细胞株培养上清组(1.54±0.03)减少(P<0.05)。结论CsA抑制巨噬细胞诱导T-bet的生成,可能是其在再障治疗中发挥免疫抑制作用的途径之一。 Objective To study the effect of cyclosporine A(CsA)on transcription factor T-bet of T helper 1 type ceils stimulated by mice bone marrow macrophage cell lines Ana-1 and evaluate their immunosuuppressive effects in treatment of aplastic anemia(AA). Methods (1)stimulated by supematant of cultured mice bone marrow macrophage cell lines Ana-1 ,mRNA expression of T-bet in peripheral blood mononuclear cells (PBMC) in normal mice was measured by reverse transcription polymerase chain reaction (RT-PCR). (2)stimulated by supematant of cultured Ana-1 cell lines and CsA,mRNA expression of T-bet was measured by RT-PCR. Results (1)stimulated by Ana-1 cell lines, the expression of T-bet in PBMC in normal mice was 1.54 ± 0.03, which was higher than that of normal controls ( 1.03 ± 0.06) (P〈0.05). (2)the expression of T-bet was 0.66± 0.02 after supematant of cultured Ana-1 cell lines and 1 mg/L CsA being added, which was less than that only stimulated by supernatant of cultured Ana-1 cell lines (1.54±0.03) (P〈 0.05). Conclusion It may be one of its immunosuppressive effects in treatment of AA that CsA restrains the production of T-bet.
出处 《山西医药杂志(上半月)》 CAS 2008年第3期214-216,共3页 Shanxi Medical Journal
关键词 亲环素A 贫血 再生障碍性 小鼠 巨噬细胞株Ana-1 Cyclosporine A Anemia aplastic Macrophage cell lines Ana-1
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  • 1[1]Selleri C,Maciejewski JP,Sato T,et al.Interferon-gamma constitutively expressed in the stromal microenvironment of human marrow cultures mediates potent hematopoietic inhibition.Blood,1996,87:4149-4157.
  • 2[2]Shao Z,Chu Y,Zhang Y,et al.Treatment of severe aplastic anemia with an immunosuppressive agent plus recombinant human granulocyte-macrophage colony-stimulating factor and erythropoietin.Am J Hematol,1998,59(3):185-191.
  • 3何广胜,邵宗鸿,张益枝,刘鸿,李克,宋鲁燕,郑以洲,陈桂彬,和虹,赵明峰,施均,张泓,储榆林,钱林生,杨天楹,杨崇礼.序贯强化免疫抑制并用造血生长因子治疗重型再生障碍性贫血[J].中华血液学杂志,2001,22(4):177-181. 被引量:41
  • 4和虹,邵宗鸿.再生障碍性贫血患者的T淋巴细胞研究进展[J].中华血液学杂志,1999,20(10):553-555. 被引量:32
  • 5[5]Solomou EE,Keyvanfar K,Young NS.T-bet,a Th1 transcription factor,is up-regulated in T cells from patients with aplastic anemia.Blood,2006,107(10):3983-3991.
  • 6[6]Szabo SJ,Kim ST,Costa GL,et al.A novel transcription factor,T-bet,directs Th1 lineage commitment.Cell,2000,100(6):655-669.
  • 7[7]Lugo-Villarino G,Maldonado-Lopez R,Possemato R,et al.T-bet is required for optimal production of IFN-γ and antigen-specific T cell activation by dendritic cells.Proc Natl Acad Sci USA,2003,100(13):7749-7754.
  • 8[8]Szabo SJ,Sullivan BM,Stemmann C,et al.Distinct effects of T-bet in TH1 lineage commitment and IFN-gamma production in CD4 and CD8 T cells.Science,2002,295(5553):338-342.
  • 9[9]Hofer T,Nathansen H,Lohning M,et al.GATA-3 transcriptional imprinting in Th2 lymphocytes:a mathematical mode.Proc Natl Acad Sci USA,2002,99(14):9364-9368.
  • 10[10]Chakir H,Wang H,Lefebvre DE,et al.T-bet/GATA-3 ratio as a measure of the Th1/Th2 cytokine profile in mixed cell populations:predominant role of GATA-3.J Immunol Methods,2003,278(1-2):157-169.

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