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转化生长因子-β1增强巨噬细胞集落刺激因子对人骨髓的活性。

Transforming growth factor-beta 1 augments macrophage-colony stimulating factor activity on human marrow.

作者信息

Rosenfeld C S

机构信息

Western Pennsylvania Cancer Institute, West Penn Hospital, Pittsburgh.

出版信息

Stem Cells. 1994 Sep;12(5):527-32. doi: 10.1002/stem.5530120509.

Abstract

Transforming growth factor-beta 1 (TGF-beta 1) suppresses the colony stimulating activity of most cytokines. The effect of TGF-beta 1 on macrophage colonies induced by macrophage colony stimulating factor (M-CSF) from human marrow has not been described. Experiments were performed with phenylalanine methyl ester (PME) treated marrow. PME (5 mM) eliminates stromal cells and monocytes. Colony stimulatory factors were used at plateau concentrations. TGF-beta 1 (0.1 ng/ml) significantly (p < 0.05) augmented M-CSF induced macrophage colony forming units (CFU-M) by twofold to fourfold in 8/8 donors. In contrast, colonies stimulated by granulocyte-macrophage CSF (GM-CSF) (CFU-GM), were significantly decreased by TGF-beta 1. To determine if TGF-beta 1 was present in effective concentrations in vitro, cultures were performed with anti-TGF-beta 1. Anti-TGF-beta 1 decreased (p < 0.05) M-CSF induced colonies in 5/6 donors. The method of TGF-beta 1 enhancement was explored with antihuman CSF-1 receptor antibody. Antihuman CSF-1 receptor antibody resulted in comparable suppression of CFU-M resulting from both M-CSF and M-CSF + TGF-beta 1. These studies indicate that TGF-beta 1 directly enhances M-CSF activity by a mechanism other than upregulation of M-CSF receptors.

摘要

转化生长因子-β1(TGF-β1)可抑制大多数细胞因子的集落刺激活性。TGF-β1对人骨髓中巨噬细胞集落刺激因子(M-CSF)诱导的巨噬细胞集落的影响尚未见报道。实验采用苯丙氨酸甲酯(PME)处理的骨髓进行。PME(5 mM)可清除基质细胞和单核细胞。集落刺激因子使用的是平台浓度。TGF-β1(0.1 ng/ml)在8/8例供体中使M-CSF诱导的巨噬细胞集落形成单位(CFU-M)显著(p < 0.05)增加了两倍至四倍。相比之下,粒细胞-巨噬细胞集落刺激因子(GM-CSF)刺激的集落(CFU-GM)则被TGF-β1显著减少。为了确定体外是否存在有效浓度的TGF-β1,使用抗TGF-β1进行培养。抗TGF-β1在5/6例供体中使M-CSF诱导的集落减少(p < 0.05)。用抗人CSF-1受体抗体探索了TGF-β1增强的机制。抗人CSF-1受体抗体对M-CSF和M-CSF + TGF-β1诱导的CFU-M产生了相当的抑制作用。这些研究表明,TGF-β1通过一种不同于上调M-CSF受体的机制直接增强M-CSF活性。

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