Spets H, Georgii-Hemming P, Siljason J, Nilsson K, Jernberg-Wiklund H
Department of Genetics and Pathology, Unit of Pathology, University Hospital, Uppsala, Sweden.
Blood. 1998 Oct 15;92(8):2914-23.
A poor response to Fas-induced apoptosis is evident in some multiple myeloma (MM) cell lines and primary cells. In this study, we have examined the possibility to increase the sensitivity to Fas-induced apoptosis by pretreatment of MM cells with interferon-gamma (IFN-gamma) or interferon-alpha (IFN-alpha). Both IFN-gamma and IFN-alpha markedly increased the Fas-induced apoptosis in all cell lines tested (U-266-1970, U-266-1984, and U-1958). In the U-266-1970 and U-1958 cell lines, pretreatment with either IFN-gamma or IFN-alpha also inhibited proliferation in a dose-dependent manner. In contrast, IFN-gamma activation of the Fas death pathway in the U-266-1984 cells was not accompanied by growth inhibition. Incubation with the IFNs increased the Fas antigen expression in one of three cell lines but did not alter the expression of Bcl-2 or Bax. The IFNs are important regulators of growth and survival in MM cells. Our results suggest that activation of Fas-mediated apoptosis is a novel mechanism by which the IFNs exert inhibitory effects on MM cells.
在一些多发性骨髓瘤(MM)细胞系和原代细胞中,对Fas诱导的凋亡反应较差是显而易见的。在本研究中,我们检测了用γ干扰素(IFN-γ)或α干扰素(IFN-α)预处理MM细胞来增加对Fas诱导凋亡敏感性的可能性。IFN-γ和IFN-α均显著增加了所有测试细胞系(U-266-1970、U-266-1984和U-1958)中Fas诱导的凋亡。在U-266-1970和U-1958细胞系中,用IFN-γ或IFN-α预处理也以剂量依赖的方式抑制增殖。相比之下,U-266-1984细胞中Fas死亡途径的IFN-γ激活并未伴随生长抑制。用IFN孵育增加了三个细胞系之一中的Fas抗原表达,但未改变Bcl-2或Bax的表达。IFN是MM细胞生长和存活的重要调节因子。我们的结果表明,Fas介导的凋亡激活是IFN对MM细胞发挥抑制作用的一种新机制。