Department of Biochemistry and Molecular Biology, Graduate School of Medical Science, Yamagata University, Japan.
Department of Biochemical Engineering, Graduate School of Science and Engineering, Yamagata University, Yonezawa, Yamagata 992-8510, Japan.
J Immunol Methods. 2021 Feb;489:112912. doi: 10.1016/j.jim.2020.112912. Epub 2020 Nov 12.
Ferroptosis is regulated, non-apoptotic cell death in which ferrous iron and lipid peroxidation products play essential roles. While the ferroptotic pathway is now becoming unveiled, it is difficult to determine its involvement in situ because no unique marker for ferroptotic cells is known. In this study, we report on raising a rat monoclonal antibody against mouse-derived Hepa 1-6 cells that had been cultivated in cystine-deprived media. Binding of the resulting antibody, designated as FerAb, increased during advancing ferroptosis which was caused, not only by cystine deprivation but also treatment with erastin or RSL3, while apoptotic cell death induced by a staurosporine treatment had no effect on the binding. The FerAb was found to bind to 4-hydroxy-2-nonenal (HNE)-modified bovine serum albumin, but no specific protein was detected in ferroptotic cells in an immunoblot analysis. These results indicate that non-proteinaceous, HNE-like structural moiety was part of the antigen for FerAb, although the binding profiles of FerAb to ferroptotic cells were different from those of the currently available anti-HNE antibody. Immunocytological detection revealed inhomogenous staining within cells and partial co-localization with peripheral mitochondria and other cellular components. FerAb was found to be applicable for ferroptotic cells in other mouse cells and cultured human cells that were examined. Thus, the properties of the rat monoclonal antibody FerAb established in this study promise to be useful for the characterization of ferroptotic cell death.
铁死亡是一种受调控的非凋亡性细胞死亡形式,亚铁离子和脂质过氧化产物在其中发挥着重要作用。尽管铁死亡途径正在被揭示,但由于目前还不知道铁死亡细胞的特有标志物,因此很难确定其在体内的参与情况。在这项研究中,我们报告了一种针对在胱氨酸缺乏的培养基中培养的鼠源性 Hepa 1-6 细胞的大鼠单克隆抗体的产生。该抗体被命名为 FerAb,在铁死亡进展过程中结合增加,这不仅是由胱氨酸缺乏引起的,而且用 erastin 或 RSL3 处理也会引起这种结合,而用 staurosporine 处理引起的凋亡性细胞死亡对结合没有影响。FerAb 被发现与 4-羟基-2-壬烯醛(HNE)修饰的牛血清白蛋白结合,但在免疫印迹分析中未在铁死亡细胞中检测到特定的蛋白质。这些结果表明,非蛋白类的 HNE 样结构部分是 FerAb 的抗原的一部分,尽管 FerAb 与铁死亡细胞的结合模式与现有的抗 HNE 抗体不同。免疫细胞化学检测显示细胞内存在不均匀染色,部分与周围的线粒体和其他细胞成分共定位。FerAb 被发现可用于其他小鼠细胞和培养的人类细胞中的铁死亡细胞。因此,本研究中建立的大鼠单克隆抗体 FerAb 的特性有望用于铁死亡细胞死亡的特征描述。