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新鲜人急性非淋巴细胞白血病细胞分泌肿瘤坏死因子-α:对正常CFU-GM祖细胞消失的作用

Secretion of tumor necrosis factor-alpha by fresh human acute nonlymphoblastic leukemic cells: role in the disappearance of normal CFU-GM progenitors.

作者信息

Kobari L, Weil D, Lemoine F M, Dubois C, Thiam D, Baillou C, Guigon M, Gorin N C, Najman A

机构信息

Department of Hematology, Faculty of Medicine, St. Antoine, Paris, France.

出版信息

Exp Hematol. 1990 Dec;18(11):1187-92.

PMID:1699775
Abstract

The disappearance of normal hematopoiesis during acute nonlymphoblastic leukemia (ANLL) is poorly understood. Several reports indicate that conditioned medium obtained from leukemic cells might inhibit the formation of normal hematopoietic progenitors. However, these blast-conditioned medium (BCM) inhibitory activities are not well characterized. In order to evaluate whether BCM might contain an activity inhibiting the growth of normal marrow progenitors, BCM from 13 consecutive patients with ANLL were tested on normal bone marrow in methylcellulose assays. In all the cases, a significant inhibition of the growth of granulocyte-macrophage colony-forming unit (CFU-GM) progenitors was observed, whereas erythroid burst-forming unit (BFU-E) progenitors were not affected. Further characterization of the BCM inhibitory activity showed using both a biological assay and RIA, the presence of tumor necrosis factor-alpha (TNF-alpha) in 10 out of 13 BCM. Northern blot analysis performed in six patients showed a correlation between the expression of TNF-alpha mRNA by leukemic cells and the presence of TNF-alpha in BCM. Moreover, the BCM inhibitory activity could be neutralized with an anti-TNF-alpha antiserum. These data indicate that leukemic cells express and release frequently TNF-alpha, which may therefore play an important role in the inhibition of granulopoiesis during leukemia.

摘要

急性非淋巴细胞白血病(ANLL)期间正常造血功能的消失目前尚不清楚。一些报告表明,从白血病细胞获得的条件培养基可能会抑制正常造血祖细胞的形成。然而,这些原始细胞条件培养基(BCM)的抑制活性尚未得到很好的表征。为了评估BCM是否可能含有抑制正常骨髓祖细胞生长的活性,在甲基纤维素试验中,对13例连续ANLL患者的BCM进行了正常骨髓检测。在所有病例中,均观察到粒细胞-巨噬细胞集落形成单位(CFU-GM)祖细胞的生长受到显著抑制,而红系爆式集落形成单位(BFU-E)祖细胞未受影响。BCM抑制活性的进一步表征显示,使用生物学检测和放射免疫分析(RIA),13份BCM中有10份存在肿瘤坏死因子-α(TNF-α)。对6例患者进行的Northern印迹分析表明,白血病细胞中TNF-α mRNA的表达与BCM中TNF-α的存在之间存在相关性。此外,BCM的抑制活性可以被抗TNF-α抗血清中和。这些数据表明,白血病细胞频繁表达和释放TNF-α,因此TNF-α可能在白血病期间粒细胞生成的抑制中起重要作用。

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