Department of Obstetrics and Gynecology, Graduate School of Medical Sciences, Kanazawa University, Takara-machi 13-1, Kanazawa, Ishikawa, 920-8640, Japan.
Department of Virology II, National Institute of Infectious Diseases, Tokyo, 162-8640, Japan.
Sci Rep. 2021 Feb 15;11(1):3833. doi: 10.1038/s41598-021-83529-x.
Activation-induced cytidine deaminase (AID, Aicda) is a master gene regulating class switching of immunoglobulin genes. In this study, we investigated the significance of AID expression in the ovary. Immunohistological study and RT-PCR showed that AID was expressed in murine granulosa cells and oocytes. However, using the Aicda-Cre/Rosa-tdRFP reporter mouse, its transcriptional history in oocytes was not detected, suggesting that AID mRNA in oocytes has an exogenous origin. Microarray and qPCR validation revealed that mRNA expressions of growth differentiation factor-9 (GDF-9) in oocytes and stem cell factor (SCF) in granulosa cells were significantly decreased in AID-knockout mice compared with wild-type mice. A 6-h incubation of primary granuloma cells markedly reduced AID expression, whereas it was maintained by recombinant GDF-9. In contrast, SCF expression was induced by more than threefold, whereas GDF-9 completely inhibited its increase. In the presence of GDF-9, knockdown of AID by siRNA further decreased SCF expression. However, in AID-suppressed granulosa cells and ovarian tissues of AID-knockout mice, there were no differences in the methylation of SCF and GDF-9. These findings suggest that AID is a novel candidate that regulates cross-talk between oocytes and granulosa cells through a GDF-9 and SCF feedback system, probably in a methylation-independent manner.
激活诱导胞嘧啶脱氨酶(AID,Aicda)是调节免疫球蛋白基因类别转换的主基因。在这项研究中,我们研究了 AID 在卵巢中的表达意义。免疫组织化学研究和 RT-PCR 表明 AID 在小鼠颗粒细胞和卵母细胞中表达。然而,使用 Aicda-Cre/Rosa-tdRFP 报告小鼠,未检测到其在卵母细胞中的转录史,这表明卵母细胞中的 AID mRNA 具有外源性来源。微阵列和 qPCR 验证显示,与野生型小鼠相比,AID 敲除小鼠的卵母细胞中生长分化因子 9(GDF-9)和颗粒细胞中干细胞因子(SCF)的 mRNA 表达显著降低。原代颗粒细胞孵育 6 小时可显著降低 AID 表达,但重组 GDF-9 可维持其表达。相比之下,SCF 表达增加了三倍以上,而 GDF-9 完全抑制了其增加。在 GDF-9 存在的情况下,siRNA 敲低 AID 进一步降低了 SCF 的表达。然而,在 AID 抑制的颗粒细胞和 AID 敲除小鼠的卵巢组织中,SCF 和 GDF-9 的甲基化没有差异。这些发现表明,AID 是一种通过 GDF-9 和 SCF 反馈系统调节卵母细胞和颗粒细胞之间串扰的新候选物,可能以非甲基化依赖的方式。