Matsuda Fuko, Inoue Naoko, Maeda Akihisa, Cheng Yuan, Sai Takafumi, Gonda Hiroshi, Goto Yasufumi, Sakamaki Kazuhiro, Manabe Noboru
Research Unit for Animal Life Sciences, Animal Resource Science Center, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Ibaraki, Japan.
J Reprod Dev. 2011 Feb;57(1):151-8. doi: 10.1262/jrd.10-124h. Epub 2010 Nov 6.
In mammalian ovaries, most follicles are lost by atresia before ovulation. It has become apparent that the apoptosis of granulosa cells induces follicular atresia. Forkhead box O3 (FOXO3), also called FKHRL1 (forkhead in rhabdomyosarcoma-like 1), is a proapoptotic molecule that belongs to the FOXO subfamily of forkhead transcription factors. Foxo3-deficient female mice were reported to be infertile because of abnormal ovarian follicular development, but the precise influences of FOXO3 on follicular atresia of mature ovary have not been determined. Therefore, we examined the expression and function of FOXO3 in porcine ovarian follicles and granulosa-derived cells. FOXO3 mRNA levels in granulosa cells of porcine ovaries increased during atresia, while FOXO3 protein was abundant in granulosa cells of early atretic follicles. By immunohistochemistry, the inner surface area of the granulosa layer in early atretic follicles was strongly stained with anti-FOXO3 antibody. The granulosa cells expressing FOXO3 coincided with apoptotic cells, indicating a role of FOXO3 as a proapoptotic factor in granulosa cells of porcine ovaries. In porcine (JC-410) and human (KGN) granulosa-derived cells, cell death was induced by transfection of FOXO3 expression vectors. Expression of the proapoptotic factors Fas ligand (FASLG) and BCL2-like 11 (BCL2L11) was upregulated by FOXO3 in KGN cells. In conclusion, FOXO3 is expressed in porcine ovarian follicles and induces apoptosis in granulosa cells, suggesting that it is a candidate for the initiator of follicular atresia.
在哺乳动物卵巢中,大多数卵泡在排卵前因闭锁而丢失。现已明确,颗粒细胞凋亡会诱导卵泡闭锁。叉头框O3(FOXO3),也称为横纹肌肉瘤样1中的叉头(FKHRL1),是一种促凋亡分子,属于叉头转录因子的FOXO亚家族。据报道,Foxo3基因缺陷的雌性小鼠因卵巢卵泡发育异常而不育,但FOXO3对成熟卵巢卵泡闭锁的确切影响尚未确定。因此,我们研究了FOXO3在猪卵巢卵泡和颗粒细胞来源细胞中的表达及功能。猪卵巢颗粒细胞中FOXO3 mRNA水平在闭锁过程中升高,而FOXO3蛋白在早期闭锁卵泡的颗粒细胞中含量丰富。通过免疫组织化学方法,早期闭锁卵泡颗粒层的内表面积被抗FOXO3抗体强烈染色。表达FOXO3的颗粒细胞与凋亡细胞一致,表明FOXO3在猪卵巢颗粒细胞中作为促凋亡因子发挥作用。在猪(JC - 410)和人(KGN)颗粒细胞来源细胞中,转染FOXO3表达载体可诱导细胞死亡。在KGN细胞中,FOXO3上调了促凋亡因子Fas配体(FASLG)和BCL2样11(BCL2L11)的表达。总之,FOXO3在猪卵巢卵泡中表达并诱导颗粒细胞凋亡,提示它可能是卵泡闭锁起始因子的候选分子。