De Nichilo M O, Burns G F
Cancer Research Unit, Faculty of Medicine, University of Newcastle, Callaghan, New South Wales, Australia.
J Cell Physiol. 1995 Aug;164(2):223-31. doi: 10.1002/jcp.1041640202.
The role of colony-stimulating factors (CSFs) in regulating the synthesis of thrombospondin 1 (TSP1) by cultured human macrophages is investigated. Macrophage (M)-CSF is shown rapidly and transiently to induce two predominant species of TSP1 mRNA. One of these species was 3.2 kb in size and appeared to be specific to M-CSF-stimulated macrophages. Adherent M-CSF-treated macrophages are also shown to express abundant surface cell-associated TSP rapidly when examined by indirect immunofluorescence staining. Granulocyte-macrophage (GM)-CSF induced TSP1 mRNA at a later time point, and this was attributable to the effects of endogenous M-CSF induced by the GM-CSF; the GM-CSF-treated cells did not display surface-associated TSP after 3 hr of treatment. Analysis of the TSP1 protein synthesised by the M-CSF-treated macrophages revealed the expected trimeric form of the molecule. In addition, an unidentified 95-kDa protein was found to be covalently associated with immunoreactive TSP1, and this appeared to be specific to the macrophages as it was not found in TSP1 precipitated from other cell types. It is suggested that the induction of TSP1 by M-CSF may play an important role in the major physiological functions of macrophages.
研究了集落刺激因子(CSF)在调节培养的人巨噬细胞中血小板反应蛋白1(TSP1)合成中的作用。结果显示,巨噬细胞(M)-CSF可快速短暂地诱导两种主要的TSP1 mRNA。其中一种大小为3.2 kb,似乎是M-CSF刺激的巨噬细胞所特有的。通过间接免疫荧光染色检查发现,贴壁的经M-CSF处理的巨噬细胞也迅速表达大量与细胞表面相关的TSP。粒细胞-巨噬细胞(GM)-CSF在较晚时间点诱导TSP1 mRNA,这归因于GM-CSF诱导的内源性M-CSF的作用;GM-CSF处理的细胞在处理3小时后未显示表面相关的TSP。对经M-CSF处理的巨噬细胞合成的TSP1蛋白的分析揭示了该分子预期的三聚体形式。此外,发现一种未鉴定的95 kDa蛋白与免疫反应性TSP1共价结合,这似乎是巨噬细胞所特有的,因为在从其他细胞类型沉淀的TSP1中未发现。提示M-CSF诱导TSP1可能在巨噬细胞的主要生理功能中起重要作用。