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During capacitation Ca〓 was present on the outer surface of IAM and in the released acrosomal contents.

精子获能前内存Ca〓主要分布于顶体外膜内侧和顶体内膜与核膜之间,并在获能和顶体反应过程被动员利用;顶体反应精子Ca〓分散存在于释放的顶体内容物中和结合于顶体内膜外侧,可能与顶体酶的活性有关;(9)。

In addition, spermiogenesis includes chromatin condensation, migration of the cytoplasm and mitochondria to the caudal pole of the nucleus, formation of a moderate axial nuclear fossa containing the proximal centriole and part of the distal centriole and presence of a short cytoplasmic canal separating mitochondria from the flagellum.

另外,精子发生过程中还包括染色质浓缩,细胞质和线粒体向细胞核的尾端迁移,在核的后端中轴位置上形成中等大小的核后凹,近端中心粒和远端中心粒的一部分嵌在核后凹之内,短的胞质内陷管将线粒体与鞭毛分隔开。

Results indicated that, just like the homologous sperm of summer flounder, the cryopreservative sperm of Lateolabrax japonicas could induce diploid gynogenesis of summer flounder.

实验表明:犬齿牙鲆同源精子经80 mJ/cm2 的紫外线照射可以完全失活,冻存花鲈精子经紫外线照射后也同样具有诱导犬齿牙鲆雌核发育的能力。

Those DNA bands expressed in female parent but not in male parent also expressed in gynogenesis filial; DNA bands expressed in male parent but not in female parent didn抰 express in gynonensis, while normally expressed in dcploid control fish.

证明牙鲫雌核发育子代的遗传物质来自母本,雌核发育诱导使用的精子经过紫外线灭活后,遗传物质己被破坏,其携带的遗传信息没有传给子代,在DNA水平证明了雌核发育诱导方法和结果的可靠性。

Methods: A cytogenetic karyotype analysis was performed in 174 cases of azoospermiaand oligospermia.

对174例少精子症、无精子症的病人进行染色体核型分析。

Results In the medium and high dose F0 groups, it was observed that the atrophy and incrassation of seminiferous tubule, decrease of spermatogenesis, hyperplasia of interstitial tissue, especially in high dose groups spermatozoon abnormality and nucleolus concentration in the rats testis after DU ingestion for 14 months. The changes became more severe with the prolongation of DU ingestion. Such changes occurred in filial rats (F1) after DC ingestion for 5 months. In the medium and high dose F0 groups, it was observed that a little atrophy of kidney glomerulus, hyperplasia of interstitial tissue after DC ingestion for 14 months, and kidney glomerulus fibrosis happened after DC ingestion for 20 months, such changes occurred in filial rats (F1) after DC ingestion for 5 months In the medium and high dose F0 groups, splenic germinal center and periarterial lymphatic sheaths were hyperplasia , companies with lymphopoiesis after DC ingestion for 7 months, splenic white pulp became more small and sparse after DC ingestion for 20 months.

结果 F0代的中、高剂量组大鼠摄入贫铀14个月后可见雄性的精曲小管萎缩,管壁增厚呈空虚网状,生精细胞层次减少,间质细胞增生,但仍见有精子生成;高剂量组可见到精子呈异型性改变,细胞核浓缩深染,且随着摄入时间延长改变愈趋明显;F1代大鼠摄入贫铀5个月后就有上述改变且更为严重。F0代中、高剂量组大鼠摄入贫铀14个月后肾小球轻度萎缩,间质增生明显,20个月时肾小球萎缩纤维化;F1代大鼠摄入贫铀5个月后就有上述改变。F0代中、高剂量组摄入贫铀7个月时脾脏生发中心和淋巴鞘增生,淋巴母细胞增生活跃,20个月时脾小体减少,生发中心稀疏;F1代大鼠摄入贫铀早期和晚期有类似改变。F0和F1代高剂量组摄入贫铀早期肝脏有炎症细胞浸润,晚期骨髓有核细胞减少,脂肪细胞增加。

Double fertilization The fusion of one pollen nucleus with the egg to form the zygote and of the other pollen nucleus with a polar nucleus to form the triploid endosperm nucleus.

双受精:指花粉粒中的一个精子与胚珠中的卵细胞结合形成受精卵,另一个精核与极核结合形成三倍体的胚乳核。

A nucleus central channel was present along the nuclear longitudinal axis during spermiogenesis.

精子形成期间,核中央位置形成贯穿整个核的中央通道,并在核底部形成植入窝,中心粒位于其中。

It takes about 0.5 h for a pollen tube from germination to arrive at the micropyle. About 0.5 h after pollination, the pollen tube releases two sperms into one synergid. At 0.5-2.5 h after pollination, the egg cell fuses with one sperm to form a zygote. About 10.0 h after pollination, the division of the zygote begins. The duration of the zygote lasts about 2.5-10.0 h. However, one sperm nucleus fuses with two polar nuclei at 1.0-3.0 h after pollination, and 5.0 h after pollination the primary endosperm nucleus begins to divide.

水稻受精过程经历的时间表如下:授粉后,花粉在柱头萌发;花粉萌发至花粉管进入珠孔大约需要0.5小时;授粉后0.5小时左右,花粉管进入一个助细胞,释放精子;授粉后0.5-2.5小时,精卵融合形成合子;授粉后约10.0小时,合子第1次分裂,合子期为授粉后2.5-10.0小时;授粉后1.0-3.0小时,精核与两极核融合;授粉后约5.0小时,初生胚乳核分裂。

Methods Micronucleus test: Kuming mice were divided into 3 groups at the dibutyl phthalate dosage of 33,330,3 300 mg/kg,and the bone-narrow micronucleus test was undertaken according to the routine method.

选择妊娠期和哺乳期SD雌性大鼠,灌胃染毒,DBP剂量分别为0、125、250、500 mg/kg,计数F1代雄性大鼠的附睾尾精子数、精子活力、精子畸形率。结果DBP在3 300 mg/kg时能引起微核率的升高(P.01)。

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