Mo Xianhong, Wu Guoquan, Yuan Dianshuai, Jia Baoyu, Liu Cong, Zhu Shien, Hou Yunpeng
State Key Laboratory for Agrobiotechnology, College of Biological Sciences, China Agricultural University, Beijing, People's Republic of China.
Mol Reprod Dev. 2014 Jul;81(7):608-18. doi: 10.1002/mrd.22327. Epub 2014 May 21.
The present study was conducted to examine the effects of leukemia inhibitory factor (LIF) on bovine oocyte maturation and early embryo development in vitro. Results showed that LIF supplementation (25 ng/ml) enhanced nuclear maturation of intact cumulus-oocyte complexes (COCs) compared to the vehicle control. Similar results were observed in denuded oocytes, indicating that LIF directly influences oocyte development. LIF-treated oocytes showed a higher cortical-granule-migration rate and increased expression of CD9, a tetraspanin transmembrane protein essential for fertilization. After in vitro fertilization, oocytes receiving LIF supplementation exhibited a higher cleavage rate and yielded a significantly higher number of blastocysts. To further dissect the molecular mechanism underlying this LIF-induced bovine oocyte maturation phenotype, we examined the involvement of two signaling cascades, mitogen-activated protein kinases (MAPK3/1)- and the signal transducer and activator of transcription 3 (STAT3)-dependent pathways. Western blot results revealed that LIF phosphorylated MAPK3/1 and STAT3. Inhibition of MAPK3/1 activation with MEK inhibitor U0126 only partially blocked LIF-induced nuclear maturation, although it attenuated oocyte cytoplasmic maturation. Inhibition of JAK/STAT3 activation with a specific pharmacological inhibitor completely abolished the LIF-response in bovine oocyte. In summary, these data revealed a novel role for LIF in bovine oocyte maturation subsequent embryonic development.
本研究旨在检测白血病抑制因子(LIF)对牛卵母细胞体外成熟及早期胚胎发育的影响。结果显示,与载体对照相比,添加LIF(25 ng/ml)可提高完整卵丘-卵母细胞复合体(COCs)的核成熟率。在裸卵中也观察到了类似结果,表明LIF直接影响卵母细胞发育。经LIF处理的卵母细胞显示出更高的皮质颗粒迁移率,且参与受精过程的四跨膜蛋白CD9的表达增加。体外受精后,添加LIF的卵母细胞显示出更高的卵裂率,并且产生的囊胚数量显著增加。为了进一步剖析LIF诱导的牛卵母细胞成熟表型背后的分子机制,我们检测了有丝分裂原激活蛋白激酶(MAPK3/1)和信号转导及转录激活因子3(STAT3)依赖的两条信号通路的参与情况。蛋白质免疫印迹结果显示,LIF可使MAPK3/1和STAT3磷酸化。用MEK抑制剂U0126抑制MAPK3/1激活仅部分阻断了LIF诱导的核成熟,尽管它减弱了卵母细胞的细胞质成熟。用特异性药理抑制剂抑制JAK/STAT3激活完全消除了牛卵母细胞对LIF的反应。总之,这些数据揭示了LIF在牛卵母细胞成熟及后续胚胎发育中的新作用。