Liu Xin-Yong, Miao Yi-Long, Zhang Jie, Qiu Jian-Hua, Cui Xiang-Zhong, Gao Wei-Qiang, Luo Ming-Jiu, Tan Jing-He
College of Animal Science and Veterinary Medicine, Shandong Agricultural University, Tai-an City, P.R. China.
Cell Reprogram. 2012 Oct;14(5):436-47. doi: 10.1089/cell.2012.0029. Epub 2012 Aug 21.
A systematic study was conducted on round spermatids (ROS) injection (ROSI) using the goat model. After ROSI, the oocytes were treated or not with ionomycin (ROSI+I and ROSI-I, respectively) and compared with intracytoplasmic sperm injection (ICSI). After ROSI-I, most oocytes were arrested with premature chromatin condensation and few oocytes formed pronuclei. In contrast, most oocytes formed pronuclei after ROSI+I. Some ROS were observed to form asters that organized a dense microtubule network after ROSI+I, but after ROSI-I, no ROS asters were observed. Whereas most of the oocytes showed Ca(2+) rises and a significant decline in maturation-promoting factor (MPF) and mitogen-activated protein kinase (MAPK) activities after ROSI+I, no such changes were observed after ROSI-I. Due to the lack of Ca(2+) oscillations after ROSI-I, oocytes were injected with more ROS. Interestingly, different from the results observed in a single ROS injection, injection with four ROS effectively activated oocytes by inducing typical Ca(2+) oscillations. Whereas ROSI+I oocytes and ICSI oocytes both showed extensive microtubule networks, no such a network was observed in parthenogenetic oocytes. Together, the results suggest that goat ROS is not able to trigger intracellular Ca(2+) rises and thus to inhibit MPF and MAPK activities, but artificial activation improved fertilization and development of ROSI goat oocytes. Goat ROS can organize functional microtubular asters in activated oocytes. A ROS-derived factor(s) may be essential for organization of a functional microtubule network to unite pronuclei. Goat centrosome is of paternal origin because both ROS and sperm asters organized an extensive microtubule network after intra-oocyte injection.
利用山羊模型对圆形精子细胞注射(ROSI)进行了系统研究。ROSI后,卵母细胞分别用离子霉素处理或不处理(分别为ROSI+I和ROSI-I),并与卵胞浆内单精子注射(ICSI)进行比较。ROSI-I后,大多数卵母细胞因染色质过早凝聚而停滞,很少有卵母细胞形成原核。相比之下,ROSI+I后大多数卵母细胞形成了原核。在ROSI+I后,观察到一些圆形精子细胞形成星状体,这些星状体组织形成了密集的微管网络,但在ROSI-I后,未观察到圆形精子细胞星状体。虽然大多数卵母细胞在ROSI+I后显示出Ca(2+)升高以及成熟促进因子(MPF)和丝裂原活化蛋白激酶(MAPK)活性显著下降,但在ROSI-I后未观察到此类变化。由于ROSI-I后缺乏Ca(2+)振荡,因此向卵母细胞中注射了更多的圆形精子细胞。有趣的是,与单次注射圆形精子细胞所观察到的结果不同,注射四个圆形精子细胞通过诱导典型的Ca(2+)振荡有效地激活了卵母细胞。虽然ROSI+I卵母细胞和ICSI卵母细胞都显示出广泛的微管网络,但在孤雌生殖卵母细胞中未观察到这样的网络。总之,结果表明山羊圆形精子细胞不能触发细胞内Ca(2+)升高,从而不能抑制MPF和MAPK活性,但人工激活改善了ROSI山羊卵母细胞的受精和发育。山羊圆形精子细胞可以在激活的卵母细胞中组织形成功能性的微管星状体。一种源自圆形精子细胞的因子可能对于组织功能性微管网络以结合原核至关重要。山羊中心体源自父本,因为在卵母细胞内注射后,圆形精子细胞和精子星状体都组织形成了广泛的微管网络。