Suppr超能文献

协同抑制:两种集落刺激因子联合对因子依赖性造血细胞增殖的异常抑制

Synergistic suppression: anomalous inhibition of the proliferation of factor-dependent hemopoietic cells by combination of two colony-stimulating factors.

作者信息

Metcalf D, Nicola N A, Gough N M, Elliott M, McArthur G, Li M

机构信息

Walter and Eliza Hall Institute of Medical Research, Royal Melbourne Hospital, Victoria, Australia.

出版信息

Proc Natl Acad Sci U S A. 1992 Apr 1;89(7):2819-23. doi: 10.1073/pnas.89.7.2819.

Abstract

Cells of the continuous murine hemopoietic cell line FDC-P1 expressing macrophage-colony-stimulating factor (M-CSF) receptors following retroviral insertion of murine c-fms cDNA proliferated clonally when stimulated by granulocyte/macrophage (GM)-CSF, multipotential CSF, or M-CSF. However, M-CSF combined with either GM-CSF or multi-CSF, even at low CSF concentrations, strongly inhibited colony formation, with loss of clonogenicity in affected cells accompanied by increased macrophage differentiation. Stimulation by these CSF combinations did not induce short-term changes in CSF receptor expression or internalization. FDC-P1 cells expressing another inserted tyrosine kinase receptor, basic fibroblast growth factor receptor, did not exhibit suppression when GM-CSF was combined with fibroblast growth factor. This phenomenon of synergistic suppression may have relevance for the future clinical use of combinations of CSFs, because a potentially similar suppression is also observable with some normal macrophage progenitor cells.

摘要

在逆转录病毒插入小鼠c-fms cDNA后表达巨噬细胞集落刺激因子(M-CSF)受体的连续小鼠造血细胞系FDC-P1细胞,在受到粒细胞/巨噬细胞(GM)-CSF、多能CSF或M-CSF刺激时会进行克隆增殖。然而,M-CSF与GM-CSF或多能CSF联合使用时,即使在低CSF浓度下,也会强烈抑制集落形成,受影响细胞的克隆形成能力丧失,同时巨噬细胞分化增加。这些CSF组合的刺激并未诱导CSF受体表达或内化的短期变化。表达另一种插入的酪氨酸激酶受体(碱性成纤维细胞生长因子受体)的FDC-P1细胞,在GM-CSF与成纤维细胞生长因子联合使用时未表现出抑制作用。这种协同抑制现象可能与CSF组合在未来临床应用中的相关性有关,因为在一些正常巨噬细胞祖细胞中也可观察到潜在的类似抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a49f/48754/10a0be578a17/pnas01081-0323-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验