Isobe N, Terada T
Animal Science, Graduate School for International Development and Cooperation, Hiroshima University, Higashi-Hiroshima, 739-8529 Japan.
Reproduction. 2001 Feb;121(2):249-57.
The present study was undertaken to explore the regulatory mechanisms for meiotic resumption of pig cumulus-oocyte complexes (COCs) by assessing the nuclear status of oocytes, the degree of gap junction cell-to-cell communication and cumulus expansion after culture of various numbers of COCs in 10 microl droplets of medium for 24 h. Gap junction communication was examined by confocal laser scanning microscopy after injection of a fluorescent dye, lucifer yellow, into the oocytes. When one, three or six COCs were cultured in a 10 microl droplet, germinal vesicle breakdown was observed in > 70% of oocytes; increasing the number of COCs in a droplet further actually decreased the proportion of oocytes undergoing germinal vesicle breakdown (10 COCs: 49%; 20 COCs: 21%; 40 COCs: 13%). When six COCs were cultured in a 10 microl droplet of conditioned medium (prepared previously by culturing 20 intact and oocytectomized COCs for 24 h), the proportion of oocytes undergoing germinal vesicle breakdown was significantly reduced compared with the proportion in fresh medium. An increase in the proportion of category 1 COCs (all gap junctions within cumulus cells and between cumulus cells and oocyte are functionally maintained) was achieved by increasing the number of COCs cultured in a 10 microl droplet. The addition of conditioned medium to the fresh medium at a concentration of 50% significantly inhibited cumulus expansion. From these results, it is concluded that the factors secreted by cumulus cells regulate the disruption of gap junctions and cumulus expansion, and concurrently control the incidence of germinal vesicle breakdown in pig COCs.
本研究旨在通过评估卵母细胞的核状态、间隙连接细胞间通讯程度以及在10微升培养基小滴中培养不同数量的卵丘-卵母细胞复合体(COCs)24小时后的卵丘扩展情况,来探索猪COCs减数分裂恢复的调控机制。在向卵母细胞注射荧光染料荧光黄后,通过共聚焦激光扫描显微镜检查间隙连接通讯。当在10微升小滴中培养1个、3个或6个COCs时,超过70%的卵母细胞观察到生发泡破裂;进一步增加小滴中COCs的数量实际上会降低经历生发泡破裂的卵母细胞比例(10个COCs:49%;20个COCs:21%;40个COCs:13%)。当在10微升条件培养基小滴中培养6个COCs(先前通过培养20个完整的和去卵母细胞的COCs 24小时制备)时,与新鲜培养基中的比例相比,经历生发泡破裂的卵母细胞比例显著降低。通过增加在10微升小滴中培养的COCs数量,1类COCs(卵丘细胞内以及卵丘细胞与卵母细胞之间的所有间隙连接功能均得以维持)的比例增加。以50%的浓度向新鲜培养基中添加条件培养基可显著抑制卵丘扩展。从这些结果可以得出结论,卵丘细胞分泌的因子调节间隙连接的破坏和卵丘扩展,并同时控制猪COCs中生发泡破裂的发生率。