State Key Laboratory of Animal Nutrition, Key Laboratory of Animal (Poultry) Genetics Breeding and Reproduction, Ministry of Agriculture and Rural Affairs, Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.
Key Laboratory of Feed Biotechnology of Ministry of Agriculture and Rural Affairs, Feed Research Institute, Chinese Academy of Agricultural Sciences, Beijing 100081, China.
Nutrients. 2022 Aug 16;14(16):3356. doi: 10.3390/nu14163356.
Riboflavin is an essential micronutrient and a precursor of flavin mononucleotide and flavin adenine dinucleotide for maintaining cell homeostasis. Riboflavin deficiency (RD) induces cell apoptosis. Endoplasmic reticulum (ER) stress is considered to induce apoptosis, and C/EBP homologous protein (CHOP) is a key pathway involved in this process. However, whether RD-induced apoptosis is mediated by ER stress and the CHOP pathway remains unclear and needs further investigation. Therefore, the current study presents the effect of RD on ER stress and apoptosis in the human hepatoma cell line (HepG2). Firstly, cells were cultured in a RD medium (4.55 nM riboflavin) and a control (CON) medium (1005 nM riboflavin). We conducted an observation of cell microstructure characterization and determining apoptosis. Subsequently, 4-phenyl butyric acid (4-PBA), an ER stress inhibitor, was used in HepG2 cells to investigate the role of ER stress in RD-induced apoptosis. Finally, CHOP siRNA was transfected into HepG2 cells to validate whether RD triggered ER stress-mediated apoptosis by the CHOP pathway. The results show that RD inhibited cell proliferation and caused ER stress, as well as increased the expression of ER stress markers (CHOP, 78 kDa glucose-regulated protein, activating transcription factor 6) (p < 0.05). Furthermore, RD increased the cell apoptosis rate, enhanced the expression of proapoptotic markers (B-cell lymphoma 2-associated X, Caspase 3), and decreased the expression of the antiapoptotic marker (B-cell lymphoma 2) (p < 0.05). The 4-PBA treatment and CHOP knockdown markedly alleviated RD-induced cell apoptosis. These results demonstrate that RD induces cell apoptosis by triggering ER stress and the CHOP pathway.
核黄素是一种必需的微量营养素,也是黄素单核苷酸和黄素腺嘌呤二核苷酸的前体,可维持细胞内环境稳态。核黄素缺乏(RD)可诱导细胞凋亡。内质网(ER)应激被认为可诱导细胞凋亡,C/EBP 同源蛋白(CHOP)是该过程中的关键途径。然而,RD 诱导的细胞凋亡是否通过 ER 应激和 CHOP 途径介导尚不清楚,需要进一步研究。因此,本研究探讨了 RD 对人肝癌细胞系(HepG2)中 ER 应激和凋亡的影响。首先,将细胞在 RD 培养基(4.55 nM 核黄素)和对照(CON)培养基(1005 nM 核黄素)中培养。观察细胞微观结构特征并测定细胞凋亡。随后,用内质网应激抑制剂 4-苯丁酸(4-PBA)处理 HepG2 细胞,以研究内质网应激在 RD 诱导的细胞凋亡中的作用。最后,将 CHOP siRNA 转染到 HepG2 细胞中,以验证 RD 是否通过 CHOP 途径触发内质网应激介导的细胞凋亡。结果表明,RD 抑制细胞增殖并引起内质网应激,同时增加内质网应激标志物(CHOP、78 kDa 葡萄糖调节蛋白、激活转录因子 6)的表达(p<0.05)。此外,RD 增加了细胞凋亡率,增强了促凋亡标志物(B 细胞淋巴瘤 2 相关 X、Caspase 3)的表达,降低了抗凋亡标志物(B 细胞淋巴瘤 2)的表达(p<0.05)。4-PBA 处理和 CHOP 敲低显著减轻了 RD 诱导的细胞凋亡。这些结果表明,RD 通过触发内质网应激和 CHOP 途径诱导细胞凋亡。