Lima Feo, Bezerra Ftg, Souza G B, Matos Mht, van den Hurk R, Silva Jrv
1Biotechnology Nucleus of Sobral,Federal University of Ceara,Sobral,CE,Brazil.
2Nucleus of Biotechnology Applied to Ovarian Follicle Development,UNIVASF,Petrolina,Pernambuco,Brazil.
Zygote. 2018 Oct;26(5):381-387. doi: 10.1017/S0967199418000382. Epub 2018 Oct 31.
SummaryThis study aimed to investigate the effects of IL1β and TNFα on growth and maturation of oocytes from small follicles (1-3 mm) during in vitro culture. To this end, cumulus-oocyte complexes (COCs) with diameters of ~110 µm were cultured in TCM-199 medium alone or supplemented with IL1β (10 ng/ml), TNFα (10 ng/ml) or both for 48 h. The oocytes were measured at the beginning and at the end of the culture period. COCs were cultured for 20 h in pre-maturation medium and then half of the COCs of each group was destined for in vitro maturation and the remaining COCs were used to evaluate meiotic progression, mitochondrial distribution and the expression of mRNAs for GDF-9, c-Mos, Cyclin-B1 and H1foo. The results showed that COCs cultured with TNFα alone or together with IL1β had higher diameters than those cultured in control medium alone or supplemented with IL1β. Control oocytes isolated from large antral follicles (>5 mm) had heterogeneous distribution of mitochondria. Oocytes isolated from small antral follicles, that had been grown in vitro in TCM-199 alone or supplemented with TNFα had similar heterogeneous mitochondrial distribution before in vitro maturation (IVM). After IVM, mitochondria were heterogeneously distribution when cultured in TCM-199. However, when cultured with TNFα and/or IL1β, mitochondria were homogeneously distributed. Presence of TNFα and/or IL1β in TCM-199 culture medium did not influence the expression of mRNAs for GDF-9, c-Mos, Cyclin-B1 and H1foo. In conclusion, TNFα and a mixture of TNFα and IL1β both stimulated the growth of bovine oocytes during their in vitro culture, but do not influence gene expression in grown oocytes.
摘要
本研究旨在探讨白细胞介素1β(IL1β)和肿瘤坏死因子α(TNFα)对体外培养的小卵泡(1 - 3毫米)中卵母细胞生长和成熟的影响。为此,将直径约110微米的卵丘-卵母细胞复合体(COCs)在单独的TCM - 199培养基中培养,或添加IL1β(10纳克/毫升)、TNFα(10纳克/毫升)或两者,培养48小时。在培养期开始和结束时对卵母细胞进行测量。将COCs在预成熟培养基中培养20小时,然后每组一半的COCs用于体外成熟,其余的COCs用于评估减数分裂进程、线粒体分布以及生长分化因子9(GDF - 9)、原癌基因c - Mos、细胞周期蛋白B1(Cyclin - B1)和组蛋白H1foo的mRNA表达。结果显示,单独用TNFα或与IL1β一起培养的COCs直径比单独在对照培养基中或添加IL1β培养的COCs直径更大。从大的窦状卵泡(>5毫米)分离的对照卵母细胞线粒体分布不均一。从小的窦状卵泡分离的卵母细胞,在单独的TCM - 199中或添加TNFα体外培养后,在体外成熟(IVM)前具有相似的不均一线粒体分布。IVM后,在TCM - 199中培养时线粒体分布不均一。然而,当与TNFα和/或IL1β一起培养时,线粒体呈均一分布。TCM - 199培养基中存在TNFα和/或IL1β不影响GDF - 9、c - Mos、Cyclin - B1和H1foo的mRNA表达。总之,TNFα以及TNFα和IL1β的混合物在体外培养期间均刺激了牛卵母细胞的生长,但不影响已生长卵母细胞中的基因表达。