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肿瘤坏死因子α调节急性髓细胞性白血病患者新鲜原始细胞中造血生长因子基因的信使核糖核酸表达。

Tumor necrosis factor alpha modulates the messenger RNA expression of hematopoietic growth factor genes in fresh blast cells from patients with acute myeloblastic leukemia.

作者信息

Bergamaschi G, Cazzola M, Rosti V, Carlo-Stella C, Santini V, Ponchio L, Peverali F A, Della Valle G, Rossi Ferrini P, Ascari E

机构信息

Department of Internal Medicine and Medical Therapy, University of Pavia, Italy.

出版信息

Leukemia. 1991 Oct;5(10):886-91.

PMID:1961022
Abstract

Tumor necrosis factor alpha (TNF-alpha) has been previously shown to modulate the expression of hematopoietic growth factor genes in monocytes and other mesenchymal cells. As acute myeloblastic leukemia (AML) blasts can express and produce hematopoietic growth factors, the influence of TNF-alpha on the accumulation of mRNAs for c-myc, interleukin-3 (IL-3), granulocyte-macrophage colony-stimulating factor (GM-CSF), G-CSF, IL-6 and IL-1 beta was evaluated in fresh blasts from 13 patients with AML. Total cellular RNA was extracted from blast cells cultured for 24 hours with or without TNF-alpha (500 U/ml). The c-myc transcript level was decreased by TNF-alpha treatment in 9/13 cases, and increased in only one case. Among the growth factor genes, the GM-CSF gene was more often and consistently influenced by TNF-alpha, increased levels of its transcript being observed in 6/13 cases following treatment with the cytokine; in no case was there a reduction of GM-CSF mRNA. G-CSF and IL-6 transcripts were more heterogeneously influenced, whereas the IL-3 transcript was never detected in our AML samples. The IL-1 beta message was present in 8/13 untreated and in 13/13 TNF-alpha treated samples. Moreover, in untreated cells, GM-CSF, G-CSF and IL-6 expression was always associated with IL-beta expression. These findings indicate that TNF-alpha can modulate the levels of growth factor transcripts in AML blasts, and raise questions about the effects of TNF-alpha on leukemic hematopoiesis, considering that TNF-alpha, IL-1 and GM-CSF can synergistically stimulate the growth of AML clonogenic cells.

摘要

肿瘤坏死因子α(TNF-α)先前已被证明可调节单核细胞和其他间充质细胞中造血生长因子基因的表达。由于急性髓性白血病(AML)原始细胞可表达并产生造血生长因子,因此在13例AML患者的新鲜原始细胞中评估了TNF-α对c-myc、白细胞介素-3(IL-3)、粒细胞-巨噬细胞集落刺激因子(GM-CSF)、G-CSF、IL-6和IL-1β mRNA积累的影响。从在有或无TNF-α(500 U/ml)的情况下培养24小时的原始细胞中提取总细胞RNA。TNF-α处理后,13例中有9例c-myc转录水平降低,仅1例升高。在生长因子基因中,GM-CSF基因受TNF-α影响更为常见且一致,细胞因子处理后13例中有6例观察到其转录水平升高;GM-CSF mRNA水平在任何情况下均未降低。G-CSF和IL-6转录受到的影响更为异质,而在我们的AML样本中从未检测到IL-3转录。IL-1β信息在13例未经处理的样本中有8例存在,在13例经TNF-α处理的样本中均存在。此外,在未经处理的细胞中,GM-CSF、G-CSF和IL-6的表达总是与IL-1β的表达相关。这些发现表明TNF-α可调节AML原始细胞中生长因子转录水平,并引发了关于TNF-α对白血病造血作用的疑问,考虑到TNF-α、IL-1和GM-CSF可协同刺激AML克隆形成细胞的生长。

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