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    张诗坤, 张淑娟, 魏迁, 葛志娟, 闫洪超. 精囊腺液在雄性精子受精过程中的功能研究[J]. 徐州医科大学学报, 2021, 41(12): 888-892. DOI: 10.3969/j.issn.2096-3882.2021.12.005
    引用本文: 张诗坤, 张淑娟, 魏迁, 葛志娟, 闫洪超. 精囊腺液在雄性精子受精过程中的功能研究[J]. 徐州医科大学学报, 2021, 41(12): 888-892. DOI: 10.3969/j.issn.2096-3882.2021.12.005
    Function and mechanism of seminal vesicle fluid in the process of male sperm fertilization[J]. Journal of Xuzhou Medical University, 2021, 41(12): 888-892. DOI: 10.3969/j.issn.2096-3882.2021.12.005
    Citation: Function and mechanism of seminal vesicle fluid in the process of male sperm fertilization[J]. Journal of Xuzhou Medical University, 2021, 41(12): 888-892. DOI: 10.3969/j.issn.2096-3882.2021.12.005

    精囊腺液在雄性精子受精过程中的功能研究

    Function and mechanism of seminal vesicle fluid in the process of male sperm fertilization

    • 摘要: 目的 目前对于精囊腺液的功能研究较为成熟,然而其在精卵结合过程中的作用知之甚少,本文通过构建精囊腺切除小鼠模型进一步深入研究精囊腺液在精卵结合中的功能。方法 一、小鼠睾丸组织结构分析:分别构建精囊腺暴露与精囊腺切除小鼠模型,观察两组小鼠睾丸形态以及睾丸重量,并运用苏木精-伊红染色技术(hematoxylin-eosin staining, HE)分析精囊腺暴露与精囊腺切除小鼠的睾丸管腔形态结构。二、精子浓度与活力分析:采用计算机辅助精液分析仪(computer-assisted semen analysis, CASA)分析其生育力相关参数,包括精子活动力以及精子浓度。三、生育力检测:8周龄成年的精囊腺暴露小鼠和精囊腺切除小鼠分别与野生型C57BL/6雌鼠按雄:雌为1:1的比例交配,维持6个月的观察时间,观察并记录分娩频率、产仔数目以及出生小仔的健康状态,统计结果并分析。四、E7.0胚胎观察:将雌鼠按照2:1比例分别与精囊腺暴露组和精囊腺切除组交配,将捡到栓的雌鼠单独放置,6天后取子宫内胚胎拍照计数。五、体内受精实验:雌鼠6周龄雌鼠经药物促排后分别与精囊腺暴露小鼠以及精囊腺切除小鼠1:1比例合笼交配进行体内受精实验,次日手术获取体内受精原核并进行培养,实时观察并记录两组胚胎体外培养的发育情况。结果 一、与精囊腺暴露小鼠相比,精囊腺切除小鼠的睾丸形态、重量、管腔组织形态结构未有显著差异(P>0.05)。二、精囊腺切除小鼠精子活动力、精子浓度与精囊腺暴露组小鼠相比均没有明显变化(P>0.05)。三、生育力检测实验发现,精囊腺切除组雄鼠均不育,精囊腺暴露组雄鼠平均每窝产仔7只左右。四、与精囊腺切除组交配的雌鼠,未发现E7.0胚胎。五、体内受精实验表明精囊腺切除后小鼠可以部分受精形成原核,却无法形成正常的4细胞。结论 精囊腺切除小鼠部分精子可以完成受精发育成2细胞,却无法形成正常的4细胞,最终导致不育。

       

      Abstract: ob<x>jective At present, the study on the function of seminal vesicle gland fluid is relatively mature, but its role in the process of sperm-egg union is poorly understood. In this paper, the function of seminal vesicle gland fluid in sperm-egg union is further studied by generating a mouse model of seminal vesicle gland resection. Methods 1. Mouse testicular tissue structure analysis: The seminal vesicle gland exposure and seminal vesicle gland resection mouse models were generated respectively, the morphology and weight of testes were observed, and morphological structure of the testicular lumen were used hematoxylin-eosin staining ( HE) analysis. 2. Sperm concentration and viability analysis: Computer-assisted semen analysis (CASA) is used to analyze its fertility-related parameters, including sperm motility and sperm concentration. 3. Fertility test: 8-week-old adult seminal vesicles exposed mice and seminal vesicles removed mice were mated with wild-type C57BL/6 female mice at a ratio of 1:1 male to female, maintain an observation period of 6 months, observe and record the number of litters, analyze the results. 4 . Observation of E6.5 embryos: the female mice were mated with the seminal vesicle gland exposure group and the seminal vesicle gland excision group at a ratio of 2:1, and the female mice that picked up the plug were placed alone, the embryos in the uterus were taken and counted 6 days later. V. In vivo fertilization experiment: 6 weeks old female mice were mate with seminal vesicle gland-exposed mice and seminal vesicle gland-exposed mice with 1:1 ratio cages to conduct in v ivo fertilization experiments. the pronucleus in vivo fertilization was obtaine d by surgery on the next day, record the development of the two groups embryos in vitro culture in real time. Results 1. Compared with the mice exposed to the seminal vesicle glands, there were no significant differences in the morphology, weight, and luminal tissue morphology of the seminal vesicles removed mice (P>0.05). 2. Sperm motility and concentration did not change significantly compared with the seminal vesicle exposure group of mice ( P>0.05). 3. The fertility test found that the seminal vesicle gland resection group male mice were sterile, and the seminal vesicle gland exposure group male mice gave birth to about 7 litters on average. 4. E6.5 embryos were not found in female mice mated with the seminal vesicle gland excision group. 5. In vivo fertilization experiments show that mice can be partially fertilized to form pronucleus after seminal ves icle gland removal, but unable develop into normal 4 cells. Conclusion Part of the sperm of the seminal vesicle gland removed mice can complete the fertilization and develop into 2 cells, but unable form the normal 4 cells, which eventually leads to infertility.

       

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