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骨髓增生异常综合征骨髓细胞凋亡与TNF-α和Fas/FasL系统关系的研究 被引量:1

Experiment study of apoptosis of bone marrow cells and TNF-α and Fas/FasL expression in myelodysplastic syndrome.
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摘要 目的:探讨TNF-α和Fas/FasL的表达及骨髓细胞凋亡与骨髓增生异常综合征(myelodysplastic syndrome,MDS)发生发展的关系。方法:采用 ELISA法检测MDS患者骨髓单个核细胞培养上清液中TNF-α浓度,采用流式细胞术测定骨髓CD 34+细胞Fas、FasL的表达率和细胞凋亡率。结果:各型MDS患者骨髓单个核细胞培养上清液中TNF-α浓度和CD 34+细胞Fas、FasL的表达率均明显高于正常对照组(P< 0.01)。其中RA/RAS组的TNF-α浓度和CD 34+细胞Fas+表达率均明显高于RAEB和RAEB-t组(P<0.001),而RAEB与RAEB-t组组间无明显差异(P值分剐为0.115和0.239);RAEB和RAEB-t组细胞的CD 34+FasL+表迭率明显高于RA/RAS组(P值分别为0.001和0.010)。 RA/RAS和RAEB组的细胞凋亡率均高于对照组(P值均为0.000),而RAEB-t组的细胞凋亡率与对照组相近(P=0.216)。各型MDS患者 TNF-α浓度与CD34+Fas+表达率呈正相关(r=0.570,P=0.012)。而CD 34+细胞凋亡率与TNF-α浓度或CD 34+Fas+表达率之间均无直线相关关系(P值分别为0.103和0.091)。结论:MDS患者骨髓细胞的凋亡受多因素的调节,TNF-α与Fas/FasL系统介导的凋亡以及机体对其调控的失常参与了MDS骨髓无效造血的病理生理过程。 Objective: To investigate the relationship the development and occurrence of myelodysplastic syndrome and TNF-α between the Fas/ FasL expression and apoptosis bone marrow cells. Metbods:The concentration of TNF-α in the supernatant of cultured BMMC were measured by ELISA. The expression of Fas,FasL,apoptosis ratio and bone marrow CD34^+ cell were evaluated by flow cytometry. Results:The concentration of TNF-α in the supernatant of cultured BMMC and the expression of Fas and FasL of CD34^+ cell significantly increased in all types of MDS patients compared with control group(P〈0. 01). The concentration of TNF-α and the expression of CD34^+ Fas^+ in RA/RAS patients were much higher as compared with that in RAEB and RAEB-t patients( P〈 0. 001), but there was no difference between RAEB and RAEB-t patients (P = 0. 115, 0. 239). The expression of CD34^+ FasL^+ in RAEB and RAE-t patients were higher as compared with that in RA/RAS patients(P=0. 001,0. 010). Apoptosis of CD34^+ cell significantly increased in RA/RAS and RAEB patients compared with control group(P=0. 000,0. 000) ,but there was no difference between RAEB-t patients and control group(P= 0. 216). The concentration of TNF-α was positively correlated with the expression of CD34^+Fas^+ in all types of MDS patients(r=0. 570, P=0. 012), however, apoptosis of CD34^+ cells and the concentration of TNF-α or the expression of CD34^+ Fas^+ have no any statistical correlation( P= 0. 103,0. 091 ). Conclusions: apoptosis of bone marrow cells was affected by a lot of factors in MDS,the apoptosis induced by TNF-α and Fas/FasL system can involve in the ineffective hematopoiesis in MDS.
出处 《中国冶金工业医学杂志》 2006年第1期8-10,共3页 Chinese Medical Journal of Metallurgical industry
关键词 骨髓增生异常综合征 肿瘤坏死因子 FAS FasL细胞凋亡 Myelodysplastic syndrome Tumor necrosis factor Fas FasL Apoptosis
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  • 1Morel P,Hebbar M,Lai JL,et al.Cytogenetic analysis has strong independent prognostic value in de novo myelodysplastic syndromes and be incorporated in a new scoring system/a repoet on 408 cases[J].Leukemia,1993 ;7(9):1315
  • 2Kitagawa M,Saito I,Kuwata T,et al.Overexpression of tumor necrosis factor(TNF)-alpha and interferon(IFN)-gamma by bone marrow cells from patients with myelodysplastic syndromes[J].Leukemia,1997; 11(12):2049
  • 3Claessens YE,Bouscary D,Dupont J M,et al.In vitro proliferation and differentiation of erythroid progenitors from patients with myelodysplastic syndromes:evidence for Fas-dependent apoptosis[J].Blood,2002;99(5):1954
  • 4Gersuk GM,Beckham C,Loken M,et al.A role for tumor necrosis factor-α,Fas and Fas-ligand in marrow failure associated with myelodysplastic syndrome[J].Br J Haematol,1998; 103(1):176
  • 5Bouscary D,Chen Y L,Guesnu M,et al.Activity of the caspase-3/CPP32 enzyme is increased in‘early stage ' myelodysplastic syndromes with excessive apoptosis,but caspase inhibition does not enhance colony formation in vitro[J].Exp Hematol,2000;28 (7):784
  • 6Peddie CM,Wolf R,Melellan LI,et al.Oxidative DNA damage in CD34+ myelodysplastic cells is associated with intracellular redox changes and elevated plasma tumor necrosis factor-α concentration[J].Br J Haematol,1997; 99:625
  • 7Griffith TS,Ferguson TA.The role of FasL-induced apoptosis in immune privilege[J].Immunol Today,1997; 18(5):240
  • 8Kurotaki H,Tsushima Y,NagaiK,et al.apoptosis,bcl-2expression and P53 accumulation in myelodysplastic syndrome,myelodysplastic-syndrome-derived acute myelogenous leukemia and de novo acute myelogenous leukemia[J].Acta Haematol,2000; 102(3):115
  • 9Paul S,Calmels B,Regulier E.Tumor-induced immunosuppression[J].Ann Biol Clin(Paris),2002;60(2):143

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