Clezardin P, Serre C M, Trzeciak M C, Drouin J, Delmas P D
INSERM U. 234, Hôpital Edouard Herriot, Lyon, France.
Cancer Res. 1991 May 15;51(10):2621-7.
We have previously shown that thrombospondin (TSP) is synthesized and secreted by human MG-63 osteosarcoma cells. In this study, the secretion and cell surface expression of TSP by two different human osteosarcoma cell lines (MG-63 and TE-85) as well as the involvement of TSP in the platelet-aggregating activity of these tumor cells were studied. Using a sandwich enzyme-linked immunosorbent assay, MG-63 cells secreted 3-fold as much TSP as TE-85 cells at 48 h (0.17 +/- 0.01 (SD) versus 0.06 +/- 0.006 micrograms/10(6) cells, P = 0.007). Binding of exogenous 125I-TSP to MG-63 and TE-85 cells in monolayer indicated that binding was time and concentration dependent, saturable, and inhibited by excess cold TSP. However, despite a similar affinity, MG-63 cells had 10-fold more TSP-binding sites than TE-85 cells (402,394 +/- 130,346 versus 36,748 +/- 7,708 TSP-binding sites/cell; P = 0.002). Similar binding differences of 125I-TSP were observed with both osteosarcoma cell lines in suspension. A fluorescence-activated cell-sorting analysis was used in conjunction with an anti-TSP polyclonal antibody, and binding of endogenous TSP to MG-63 and TE-85 cells in suspension was investigated. Addition of an anti-TSP antibody to MG-63 and TE-85 cells in suspension increased the mean fluorescence intensity 50-fold when compared to an irrelevant antibody. Moreover, the fluorescence intensity of MG-63 cells with an anti-TSP polyclonal antibody was increased by 40% when compared to TE-85 cells. Since TSP was expressed on the surface of osteosarcoma cells, the involvement of this glycoprotein in the platelet-aggregating activity of MG-63 and TE-85 cells was therefore investigated using an anti-TSP polyclonal antibody and two monoclonal antibodies (P10 and MA-II), the epitopes of which lie within the Mr 140,000 non-heparin-binding fragment and the Mr 25,000 heparin-binding fragment of TSP, respectively. Preincubation of MG-63 cells (1 x 10(6) cells/ml) with either an anti-TSP polyclonal antibody (100 micrograms/ml) or monoclonal antibody P10 (15 micrograms/ml) inhibited by 80% other platelet-aggregating activity of these tumor cells, while anti-TSP monoclonal antibody MA-II (15 micrograms/ml) had no effect. In sharp contrast, the anti-TSP polyclonal antibody (100 micrograms/ml) only exhibited a slight inhibitory effect on platelet aggregation induced by TE-85 cells when using a low concentration of tumor cells (0.6 x 10(6) cells/ml).(ABSTRACT TRUNCATED AT 400 WORDS)
我们之前已经表明,血小板反应蛋白(TSP)由人MG - 63骨肉瘤细胞合成并分泌。在本研究中,我们对两种不同的人骨肉瘤细胞系(MG - 63和TE - 85)中TSP的分泌及细胞表面表达,以及TSP在这些肿瘤细胞的血小板聚集活性中的作用进行了研究。采用夹心酶联免疫吸附测定法,在48小时时,MG - 63细胞分泌的TSP量是TE - 85细胞的3倍(0.17±0.01(标准差)对0.06±0.006微克/10⁶细胞,P = 0.007)。外源性¹²⁵I - TSP与单层培养的MG - 63和TE - 85细胞的结合表明,这种结合具有时间和浓度依赖性、可饱和性,且可被过量的冷TSP抑制。然而,尽管亲和力相似,但MG - 63细胞的TSP结合位点比TE - 85细胞多10倍(402,394±130,346对36,748±7,708个TSP结合位点/细胞;P = 0.002)。在悬浮培养的两种骨肉瘤细胞系中也观察到了¹²⁵I - TSP类似的结合差异。结合抗TSP多克隆抗体,使用荧光激活细胞分选分析研究了内源性TSP与悬浮培养的MG - 63和TE - 85细胞的结合。与无关抗体相比,向悬浮培养的MG - 63和TE - 85细胞中加入抗TSP抗体可使平均荧光强度增加50倍。此外,与TE - 85细胞相比,MG - 63细胞用抗TSP多克隆抗体处理后的荧光强度增加了40%。由于TSP在骨肉瘤细胞表面表达,因此我们使用抗TSP多克隆抗体和两种单克隆抗体(P10和MA - II)研究了这种糖蛋白在MG - 63和TE - 85细胞的血小板聚集活性中的作用,这两种单克隆抗体的表位分别位于TSP的分子量为140,000的非肝素结合片段和分子量为25,000的肝素结合片段内。用抗TSP多克隆抗体(100微克/毫升)或单克隆抗体P10(15微克/毫升)对MG - 63细胞(1×10⁶细胞/毫升)进行预孵育,可抑制这些肿瘤细胞80%的其他血小板聚集活性,而抗TSP单克隆抗体MA - II(15微克/毫升)则无作用。与之形成鲜明对比的是,当使用低浓度肿瘤细胞(0.6×10⁶细胞/毫升)时,抗TSP多克隆抗体(100微克/毫升)对TE - 85细胞诱导的血小板聚集仅表现出轻微的抑制作用。(摘要截断于400字)