Matsue H, Kobayashi H, Hosokawa T, Akitaya T, Ohkawara A
Department of Dermatology, Hokkaido University School of Medicine, Sapporo, Japan.
Arch Dermatol Res. 1995;287(3-4):315-20. doi: 10.1007/BF01105085.
The Fas antigen is a cell surface protein that can mediate apoptosis in many cell types. Although its physiological function is still unclear, recent evidence indicates that this surface molecule is involved in apoptosis in the immune system and the liver. The epidermis is an organ that undergoes terminal differentiation with the eventual death of keratinocytes, and it has been suggested that this is a specialized form of apoptosis. In the present study, we examined whether or not the Fas antigen is involved in keratinocyte apoptosis. Immunoreactivity for the Fas antigen was found throughout the epidermis in normal human skin sections and cultured normal human keratinocytes, and mRNA for the Fas antigen was found to be constitutively expressed in normal epidermis and cultured normal keratinocytes by RT-PCR analysis. To determine whether the Fas antigen in keratinocytes is functional, we used a cytotoxic monoclonal antibody (mAb) against the Fas antigen to induce apoptosis. This antibody did not induce apoptosis of cultured keratinocytes even though they expressed the Fas antigen. We then tested the ability of several cytokines (TGF beta, TNF alpha and IFN gamma) to induce Fas-mediated keratinocyte apoptosis. Only pretreatment with IFN gamma followed by the addition of the anti-Fas mAb induced apoptosis, as assessed by cell viability, morphological changes and ultrastructural characteristics, suggesting that constitutive expression of the Fas antigen is not sufficient to induce apoptosis in keratinocytes and that keratinocyte apoptosis via the Fas antigen-mediated mechanism may require the activation of keratinocytes by IFN gamma, which is thought to be produced by activated T cells.(ABSTRACT TRUNCATED AT 250 WORDS)
Fas抗原是一种细胞表面蛋白,可介导多种细胞类型的凋亡。尽管其生理功能尚不清楚,但最近的证据表明,这种表面分子参与免疫系统和肝脏的凋亡过程。表皮是一个经历终末分化并最终导致角质形成细胞死亡的器官,有人认为这是一种特殊形式的凋亡。在本研究中,我们检测了Fas抗原是否参与角质形成细胞的凋亡。在正常人皮肤切片和培养的正常人角质形成细胞的整个表皮中均发现了Fas抗原的免疫反应性,并且通过逆转录聚合酶链反应(RT-PCR)分析发现,Fas抗原的mRNA在正常表皮和培养的正常角质形成细胞中组成性表达。为了确定角质形成细胞中的Fas抗原是否具有功能,我们使用了一种针对Fas抗原的细胞毒性单克隆抗体(mAb)来诱导凋亡。尽管培养的角质形成细胞表达Fas抗原,但该抗体并未诱导其凋亡。然后,我们测试了几种细胞因子(转化生长因子β、肿瘤坏死因子α和干扰素γ)诱导Fas介导的角质形成细胞凋亡的能力。只有先用干扰素γ预处理,然后加入抗Fas单克隆抗体才能诱导凋亡,这通过细胞活力、形态变化和超微结构特征进行评估,表明Fas抗原的组成性表达不足以诱导角质形成细胞凋亡,并且通过Fas抗原介导的机制导致的角质形成细胞凋亡可能需要干扰素γ激活角质形成细胞,而干扰素γ被认为是由活化的T细胞产生的。(摘要截短于250字)