School of Biomedicine, Robinson Research Institute, The University of Adelaide, Adelaide, SA, Australia.
PLoS One. 2024 Aug 7;19(8):e0308168. doi: 10.1371/journal.pone.0308168. eCollection 2024.
The ovarian KGN granulosa-like tumour cell line is commonly used as a model for human granulosa cells, especially since it produces steroid hormones. To explore this further, we identified genes that were differentially expressed by KGN cells compared to primary human granulosa cells using three public RNA sequence datasets. Of significance, we identified that the expression of the antioxidant gene TXNRD1 (thioredoxin reductase 1) was extremely high in KGN cells. This is ominous since cytochrome P450 enzymes leak electrons and produce reactive oxygen species during the biosynthesis of steroid hormones. Gene Ontology (GO) analysis identified steroid biosynthetic and cholesterol metabolic processes were more active in primary granulosa cells, whilst in KGN cells, DNA processing, chromosome segregation and kinetochore pathways were more prominent. Expression of cytochrome P450 cholesterol side-chain cleavage (CYP11A1) and cytochrome P450 aromatase (CYP19A1), which are important for the biosynthesis of the steroid hormones progesterone and oestrogen, plus their electron transport chain members (FDXR, FDX1, POR) were measured in cultured KGN cells. KGN cells were treated with 1 mM dibutyryl cAMP (dbcAMP) or 10 μM forskolin, with or without siRNA knockdown of TXNRD1. We also examined expression of antioxidant genes, H2O2 production by Amplex Red assay and DNA damage by γH2Ax staining. Significant increases in CYP11A1 and CYP19A1 were observed by either dbcAMP or forskolin treatments. However, no significant changes in H2O2 levels or DNA damage were found. Knockdown of expression of TXNRD1 by siRNA blocked the stimulation of expression of CYP11A1 and CYP19A1 by dbcAMP. Thus, with TXNRD1 playing such a pivotal role in steroidogenesis in the KGN cells and it being so highly overexpressed, we conclude that KGN cells might not be the most appropriate model of primary granulosa cells for studying the interplay between ovarian steroidogenesis, reactive oxygen species and antioxidants.
卵巢 KGN 颗粒细胞样肿瘤细胞系通常被用作人颗粒细胞的模型,特别是因为它能产生类固醇激素。为了进一步探讨这一点,我们使用三个公共 RNA 序列数据集鉴定了 KGN 细胞与原代人颗粒细胞相比差异表达的基因。值得注意的是,我们发现抗氧化基因 TXNRD1(硫氧还蛋白还原酶 1)在 KGN 细胞中的表达水平极高。这很不妙,因为细胞色素 P450 酶在类固醇激素的生物合成过程中会漏出电子并产生活性氧。基因本体论(GO)分析表明,初级颗粒细胞中类固醇生物合成和胆固醇代谢过程更为活跃,而在 KGN 细胞中,DNA 处理、染色体分离和动粒途径更为突出。细胞色素 P450 胆固醇侧链裂解(CYP11A1)和细胞色素 P450 芳香酶(CYP19A1)的表达,这对于类固醇激素孕酮和雌激素的生物合成很重要,加上它们的电子传递链成员(FDXR、FDX1、POR)在培养的 KGN 细胞中进行了测量。用 1mM 二丁酰环腺苷酸(dbcAMP)或 10μM forskolin处理 KGN 细胞,并用或不用 TXNRD1 的 siRNA 敲低。我们还检查了抗氧化基因的表达、Amplex Red 测定法测定的 H2O2 产生和 γH2Ax 染色测定的 DNA 损伤。dbcAMP 或 forskolin 处理均显著增加 CYP11A1 和 CYP19A1 的表达。然而,未发现 H2O2 水平或 DNA 损伤的显著变化。siRNA 敲低 TXNRD1 阻断了 dbcAMP 对 CYP11A1 和 CYP19A1 表达的刺激。因此,由于 TXNRD1 在 KGN 细胞的类固醇生成中起着至关重要的作用,而且它的过度表达如此之高,我们得出结论,KGN 细胞可能不是研究卵巢类固醇生成、活性氧和抗氧化剂之间相互作用的原代颗粒细胞的最佳模型。