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转化生长因子β、肿瘤坏死因子α、干扰素γ和白血病抑制因子-人抑制活性对急性髓系白血病细胞增殖的影响。

Effects of transforming growth factor beta, tumor necrosis factor alpha, interferon gamma and LIF-HILDA on the proliferation of acute myeloid leukemia cells.

作者信息

Kerangueven F, Sempere C, Tabilio A, Mannoni P

机构信息

INSERM U.119, Marseille, France.

出版信息

Eur Cytokine Netw. 1990 May-Jun;1(2):99-107.

PMID:2129395
Abstract

A group of polypeptide factors that regulate cell growth and differentiation has been tested for their biological activities on the growth and differentiation of leukemic cells isolated from patients with Acute Myeloid Leukemias (AML). The effects of Transforming Growth Factor beta 1 (TGF beta), Tumor Necrosis Factor alpha (TNF alpha), Interferon gamma (IFN gamma) and LIF-HILDA were compared on leukemic cells cultured in vitro for seven days. Spontaneously growing leukemic cells were selected in order to study either inhibition or enhancement of proliferation induced by these factors. Only TGF beta 1 was found to induce a clear inhibition of leukemic proliferation in all cases tested. Recombinant TNF alpha and IFN gamma were found to induce either inhibition or enhancement of the proliferation on separate specimens. Under the conditions of culture, it was not possible to document any effect of LIF-HILDA. Cell differentiation and cell maturation were documented studying the modulation of cell surface antigens. TGF beta did not modify antigen expression on the cells surviving after 3 days in culture. Both TNF alpha and IFN gamma were found to enhance the expression of adhesion molecules and to a lesser extent, the expression of some lineage associated antigens. No effect of LIF-HILDA on antigen modulation was documented in the cases tested. These data confirm that TGF beta is by itself a potent inhibitor of the myeloid leukemia cells proliferation.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

一组调节细胞生长和分化的多肽因子已针对其对从急性髓系白血病(AML)患者分离出的白血病细胞生长和分化的生物学活性进行了测试。比较了转化生长因子β1(TGFβ)、肿瘤坏死因子α(TNFα)、干扰素γ(IFNγ)和白血病抑制因子-人抑制活性因子(LIF-HILDA)对体外培养7天的白血病细胞的影响。选择自发生长的白血病细胞以研究这些因子诱导的增殖抑制或增强情况。在所有测试案例中,仅发现TGFβ1可明显抑制白血病增殖。发现重组TNFα和IFNγ在不同样本中分别诱导增殖抑制或增强。在培养条件下,未发现LIF-HILDA有任何作用。通过研究细胞表面抗原的调节来记录细胞分化和细胞成熟情况。TGFβ未改变培养3天后存活细胞上的抗原表达。发现TNFα和IFNγ均增强黏附分子的表达,且在较小程度上增强某些谱系相关抗原的表达。在所测试案例中,未发现LIF-HILDA对抗原调节有作用。这些数据证实,TGFβ本身是髓系白血病细胞增殖的有效抑制剂。(摘要截短至250字)

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