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作 者:胡中波[1] 游泳[1] 王良利[1] 李惠玉[1] 向建平[1] 邹萍[1]
机构地区:[1]同济医科大学附属协和医院血液病研究所,武汉430022
出 处:《临床血液学杂志》2000年第1期23-25,共3页Journal of Clinical Hematology
基 金:国家自然科学基金!资助课题(基金号39770767)
摘 要:目的:研究Fas和可溶性Fas 在急性淋巴细胞白血病(ALL)中的表达,探讨Fas在白血病细胞凋亡障碍中的作用。方法:分别用免疫组化SABC法和双抗夹心ELISA 法,检测36 例ALL患者和10 例正常对照组骨髓细胞Fas 抗原(m Fas)表达以及血浆可溶性Fas(sFas)的水平。用半定量逆转录-聚合酶链式反应(RT-PCR)检测12 例ALL患者和7 例正常对照骨髓细胞Fasm RNA 的表达。结果:36 例ALL初诊组患者Fas 抗原的表达较正常对照组低〔(6.23±6.58)%vs (28.63±5.02)% , P < 0.001〕,血浆中sFas 水平也较正常对照组低〔(11.8 176±4.7 620)ng/m lvs (27.2 874±9.2 778) ng/m l, P< 0.001〕。ALL组未见Fas m RNA经转移剪接后缺乏跨膜区的1 104 bp(对应于sFas)条带,而正常对照组可见;ALL组Fas m RNA的表达较正常对照组也显著降低(0.3 407 vs 0.8 303, P< 0.001)。结论:Fas 可能参与了白血病细胞的凋亡障碍,ALL白血病细胞可能不是通过提高血浆sFas 水平来逃避凋亡。白血病细?Objective:To study the expression of Fas and soluble Fas in acute lymphocytic leukemia (ALL) in order to elucidate its role in the failure of apoptosis in leukemias.Method:Strept avidin biotin complex method (SABC) and ELISA were respectly used to detect the expression of Fas antigen (mFas) in bone marrow cells and that of soluble Fas (sFas) in plasma in 36 ALL patients and 10 normal volunteers.Semi quantitative reverse transcriptase polymerase chain reaction (RT PCR) was used to detect the expres sion of Fas mRNA in 12 ALL patients and 7 normal volunteers.Result:The level of mFas in 36 newly diagnosed patients was significantly lower than that in the normal group 〔( 6.23 ± 6.58 )% vs ( 28.63 ± 5.02 )%,P< 0.001 )〕.The level of sFas in the plasma of ALL patients was also lower than that in the normal group ( 11.8 176 ± 4.7 620 ng/ml vs 27.2 874 ± 9.2 778 ng/ml,P< 0.001 ).The 1 104bp Fas △ TM cDNA band was not seen in ALL patients,but it was seen in the normal group.The expression of Fas mRNA in ALL patients was also lower than that in the normal group ( 0.3 407 vs 0.8 303 ,P< 0.001 ).Conclusion:The down regulation of Fas expression was related to the failure of apoptosis in leukemia.Leukemic cells were not certain to evade apoptosis by enhancing the level of sFas in plasma to block the Fas Fas ligand system.Fas in leukemic cells was regulated in the level of gene.
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