Majack R A, Goodman L V, Dixit V M
Atherosclerosis and Thrombosis Research, Upjohn Company, Kalamazoo, Michigan 49001.
J Cell Biol. 1988 Feb;106(2):415-22. doi: 10.1083/jcb.106.2.415.
Thrombospondin (TS) is an extracellular glycoprotein whose synthesis and secretion by vascular smooth muscle cells (SMC) is regulated by platelet-derived growth factor. We have used a panel of five monoclonal antibodies against TS to determine an essential role for thrombospondin in the proliferation of cultured rat aortic SMC. All five monoclonal antibodies inhibited SMC growth in 3-d and extended cell number assays; the growth inhibition was specific for anti-TS IgG. The effects of one antibody (D4.6) were examined in detail and were found to be reversable and dose dependent. Cells treated with D4.6 at 50 micrograms/ml (which resulted in a greater than 60% reduction in cell number at day 8) were morphologically identical to control cells. D4.6-treated SMC were analyzed by flow cytofluorimetry and were found to be arrested in the G1 phase of the cell cycle. To determine a possible cellular site of action of TS in cell growth, SMC were examined by immunofluorescence using a polyclonal antibody against TS. TS was observed diffusely bound to the cell surface of serum- or platelet-derived growth factor-treated cells. The binding of TS to SMC was abolished in the presence of heparin, which prevents the binding of TS to cell surfaces and inhibits the growth of SMC. Monoclonal antibody D4.6, like heparin, largely abolished cell surface staining of TS but had no detectable effect on the cellular distribution of fibronectin. These results were corroborated by metabolic labeling experiments. We conclude that cell surface-associated TS is functionally essential for the proliferation of vascular SMC, and that this requirement is temporally located in the G1 phase of the cell cycle. Agents that perturb the interaction of TS with the SMC surface, such as heparin, may inhibit SMC proliferation in this manner.
血小板反应蛋白(TS)是一种细胞外糖蛋白,血管平滑肌细胞(SMC)对其合成和分泌受血小板衍生生长因子的调节。我们使用一组针对TS的五种单克隆抗体来确定血小板反应蛋白在培养的大鼠主动脉SMC增殖中的重要作用。所有五种单克隆抗体在3天培养和细胞数量扩展试验中均抑制SMC生长;生长抑制对抗TS IgG具有特异性。详细研究了一种抗体(D4.6)的作用,发现其作用是可逆的且呈剂量依赖性。用50微克/毫升的D4.6处理细胞(这导致第8天细胞数量减少超过60%),其形态与对照细胞相同。通过流式细胞荧光术分析经D4.6处理的SMC,发现其停滞在细胞周期的G1期。为了确定TS在细胞生长中可能的细胞作用位点,使用针对TS的多克隆抗体通过免疫荧光检查SMC。观察到TS弥漫性地结合在血清或血小板衍生生长因子处理的细胞表面。在肝素存在下,TS与SMC的结合被消除,肝素可阻止TS与细胞表面结合并抑制SMC生长。单克隆抗体D4.6与肝素一样,在很大程度上消除了TS的细胞表面染色,但对纤连蛋白的细胞分布没有可检测到的影响。代谢标记实验证实了这些结果。我们得出结论,细胞表面相关的TS对于血管SMC的增殖在功能上是必不可少的,并且这种需求在时间上位于细胞周期的G1期。扰乱TS与SMC表面相互作用的试剂,如肝素,可能以这种方式抑制SMC增殖。