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粒细胞-巨噬细胞集落刺激因子与1,25-二羟基维生素D3对人单核细胞系U937分化的协同作用。

Synergistic effect of granulocyte-macrophage colony-stimulating factor and 1,25-dihydroxyvitamin D3 on the differentiation of the human monocytic cell line U937.

作者信息

Zuckerman S H, Surprenant Y M, Tang J

机构信息

Department of Immunology, Lilly Research Labs, Indianapolis, IN 46285.

出版信息

Blood. 1988 Mar;71(3):619-24.

PMID:3278748
Abstract

The human monoblastlike cell line U937 can be induced to differentiate by a variety of agents including gamma-interferon, phorbol esters, retinoic acid, and 1,25-dihydroxyvitamin D3 (VD3). Incubation of U937 with 1 to 1,000 units of recombinant human granulocyte-macrophage colony-stimulating factor (GM-CSF) did not induce macrophage differentiation. A synergistic effect on macrophage differentiation was observed, however, when U937 was cocultured with 10(-8) mol/L VD3 plus 50 U/mL GM-CSF. GM-CSF-plus VD3-treated cells demonstrated significant increases in OKM1 antigen expression, increased chemokinesis and chemotaxis, and increased Fc receptor-mediated erythrophagocytosis. Human peripheral blood monocyte cultures also demonstrated increased OKM1 antigen expression and chemotaxis when incubated with 50 to 500 U/mL of GM-CSF for 48 to 72 hours. VD3, however, was not necessary for the increases in effector function observed for GM-CSF-stimulated monocyte cultures. In distinction to the synergistic effect of GM-CSF on VD3-induced differentiation of U937, recombinant human granulocyte colony-stimulating factor (G-CSF) at comparable concentrations had no augmenting effect over that observed for VD3 alone. These results suggest that GM-CSF, in the presence of other physiological stimuli, can induce significant phenotypic changes in GM-CSF-nonresponsive cells of the monocytic lineage and can increase the effector functions of GM-CSF-responsive peripheral blood monocyte cultures.

摘要

人单核细胞样细胞系U937可被多种因子诱导分化,包括γ干扰素、佛波酯、视黄酸和1,25 - 二羟基维生素D3(VD3)。用1至1000单位的重组人粒细胞 - 巨噬细胞集落刺激因子(GM - CSF)孵育U937不会诱导巨噬细胞分化。然而,当U937与10(-8) mol/L VD3加50 U/mL GM - CSF共培养时,观察到对巨噬细胞分化有协同作用。经GM - CSF加VD3处理的细胞在OKM1抗原表达、趋化运动和趋化性以及Fc受体介导的红细胞吞噬作用方面均有显著增加。人外周血单核细胞培养物在与50至500 U/mL的GM - CSF孵育48至72小时后,也显示出OKM1抗原表达增加和趋化性增强。然而,对于GM - CSF刺激的单核细胞培养物中观察到的效应功能增加,VD3并非必需。与GM - CSF对VD3诱导的U937分化的协同作用不同,浓度相当的重组人粒细胞集落刺激因子(G - CSF)对单独VD3诱导的分化没有增强作用。这些结果表明,在存在其他生理刺激的情况下,GM - CSF可诱导单核细胞系中对GM - CSF无反应的细胞发生显著的表型变化,并可增强对GM - CSF有反应的外周血单核细胞培养物的效应功能。

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