Takahashi H, Nakamura S, Asano K, Kinouchi M, Ishida-Yamamoto A, Iizuka H
Department of Dermatology, Asahikawa Medical College, Asahikawa, Japan.
Exp Cell Res. 1999 Jun 15;249(2):291-8. doi: 10.1006/excr.1999.4476.
Interferon-gamma (IFN-gamma) induces various apoptosis-related proteins, including Fas antigen (Fas) in keratinocytes. Ultraviolet B (UVB) irradiation produces "sunburn cells," a specific type of apoptosis. Previously, we reported that IFN-gamma augments Fas-dependent apoptosis of SV40-transformed human keratinocytes (SVHK cells). Caspases are a new class of cysteine proteinases that play an important role in apoptosis. We investigated the mechanism of UVB-induced apoptosis by examining activation of the caspase cascade. UVB irradiation of SVHK cells increased the activities of caspases 1, 3, and 8, which were detected at 3 h, and peak activities occurred at 6 h. Pretreatment of SVHK cells with IFN-gamma significantly increased the activity of caspases 1, 3, and 8. UVB-induced caspase 8 stimulation was significantly suppressed only by caspase 8 inhibitor, while inhibitors of caspases 1, 3, and 8 significantly suppressed UVB-induced caspase 1 stimulation. Caspase 3 and 8 inhibitors, but not caspase 1 inhibitor, significantly suppressed UVB-induced caspase 3 activity, suggesting sequential activation of caspases 8, 3, and 1 in UVB-irradiated SVHK cells. Cross-linking and immunoprecipitation analyses showed multimerization of Fas antigen following UVB irradiation of SVHK cells. Pretreatment of SVHK cells with IFN-gamma significantly augmented UVB-induced apoptosis that was accompanied by increased Fas expression. The susceptibility to UVB-induced apoptosis was also increased in Fas-transfected SVHK cells (F2 cells). Neutralizing anti-Fas antibody significantly suppressed caspase activation and Fas-dependent apoptosis of SVHK cells and F2 cells. In contrast, UVB-induced caspase activation and apoptosis were not inhibited by neutralizing anti-Fas antibody in both cell lines. Our results suggest that UVB directly activates Fas and subsequent caspase cascade resulting in apoptosis of SVHK cells. Furthermore, the expression level of Fas antigen in keratinocytes influenced their susceptibility to UVB-induced apoptosis.
干扰素-γ(IFN-γ)可诱导角质形成细胞中多种与凋亡相关的蛋白,包括Fas抗原(Fas)。紫外线B(UVB)照射可产生“晒伤细胞”,这是一种特定类型的凋亡。此前,我们报道IFN-γ可增强SV40转化的人角质形成细胞(SVHK细胞)中Fas依赖性凋亡。半胱天冬酶是一类新型的半胱氨酸蛋白酶,在凋亡中起重要作用。我们通过检测半胱天冬酶级联反应的激活来研究UVB诱导凋亡的机制。UVB照射SVHK细胞可增加半胱天冬酶1、3和8的活性,在3小时时可检测到,峰值活性出现在6小时。用IFN-γ预处理SVHK细胞可显著增加半胱天冬酶1、3和8的活性。UVB诱导的半胱天冬酶8刺激仅被半胱天冬酶8抑制剂显著抑制,而半胱天冬酶1、3和8的抑制剂可显著抑制UVB诱导的半胱天冬酶1刺激。半胱天冬酶3和8抑制剂而非半胱天冬酶1抑制剂可显著抑制UVB诱导的半胱天冬酶3活性,提示在UVB照射的SVHK细胞中半胱天冬酶8、3和1依次激活。交联和免疫沉淀分析显示,UVB照射SVHK细胞后Fas抗原多聚化。用IFN-γ预处理SVHK细胞可显著增强UVB诱导的凋亡,并伴有Fas表达增加。在Fas转染的SVHK细胞(F2细胞)中,对UVB诱导凋亡的敏感性也增加。中和抗Fas抗体可显著抑制SVHK细胞和F2细胞中的半胱天冬酶激活和Fas依赖性凋亡。相反,在两种细胞系中,中和抗Fas抗体均未抑制UVB诱导的半胱天冬酶激活和凋亡。我们的结果表明,UVB直接激活Fas及随后的半胱天冬酶级联反应,导致SVHK细胞凋亡。此外,角质形成细胞中Fas抗原水平影响其对UVB诱导凋亡的敏感性。