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尿激酶型纤溶酶原激活因子对小鼠获能精子线粒体膜电位的影响
引用本文:丁晓芳,商学军,李红钢,官黄涛,熊承良. 尿激酶型纤溶酶原激活因子对小鼠获能精子线粒体膜电位的影响[J]. 中华男科学杂志, 2007, 13(5): 391-395
作者姓名:丁晓芳  商学军  李红钢  官黄涛  熊承良
作者单位:1. 华中科技大学,同济医学院计划生育研究所,湖北,武汉,430030;华中科技大学,附属协和医院生殖医学中心,湖北,武汉,430030
2. 南京军区南京总医院解放军临床检验医学研究所,江苏,南京,210002
3. 华中科技大学,同济医学院计划生育研究所,湖北,武汉,430030
摘    要:目的:检测尿激酶型纤溶酶原激活因子(uPA)体外对小鼠获能精子线粒体膜电位的影响。方法:采用线粒体膜电位荧光染料JC-1,利用流式细胞仪和荧光显微镜检测分别与uPA(实验组)和BWW液(对照组)共孵育0、5、15、30、60min的小鼠获能精子线粒体膜电位状态。结果:①在uPA作用第5、15min时,精子体内平均荧光强度较作用前显著增加,高膜电位的精子数量百分率相应增加(P<0.05)。②与对照组相比,实验组在uPA作用5、15min时的高膜电位精子数量百分率,以及作用15、30、60min时的精子线粒体膜电位平均荧光强度显著增加(P<0.05)。结论:uPA在体外可以增加小鼠获能精子的线粒体膜电位,并使高膜电位状态维持一段时间,为获能精子提供充足的能量供应。

关 键 词:尿激酶型纤溶酶原激活因子  精子  线粒体膜电位  JC-1荧光染料  小鼠
文章编号:1009-3591(2007)05-0391-05
收稿时间:2006-09-28
修稿时间:2006-09-282006-12-20

Effect of Urokinase-Type Plasminogen Activator on the Mitochondrial Membrane Potential of Mouse Capaciated-Spermatozoa in vitro
DING Xiao-fang,SHANG Xue-jun,LI Hong-gang,GUAN Huang-tao,XIONG Cheng-liang. Effect of Urokinase-Type Plasminogen Activator on the Mitochondrial Membrane Potential of Mouse Capaciated-Spermatozoa in vitro[J]. National journal of andrology, 2007, 13(5): 391-395
Authors:DING Xiao-fang  SHANG Xue-jun  LI Hong-gang  GUAN Huang-tao  XIONG Cheng-liang
Affiliation:1. Family Planning Research Institute, Tongji Medical College, 2. Center of Reproductive Medicine, Union Hospital, Huazhong University of Science and Technology, Wuhan, Hubei 430030, China; 3. PLA Research Institute of Clinical Laboratory Medicine, Nanjing General Hospital of Nanjing Command, Nanjing, Jiangsu 210002, China
Abstract:OBJECTIVE: To study the mechanism of uPA improving sperm capacitation by investigating the effect of uPA on the mitochondrial function of mouse capacitated-sperm in vitro. METHODS: Mitochondrial function of mouse capacitated-spermatozoa was evaluated through the assessment of mitochondrial membrane potential using JC-1 performed by flow cytometer and fluorescent microscope respectively. The experiment and the control groups were designed according to the presence or absence of uPA, each divided into 5 subgroups based on the different time of uPA treatment (or BWW in the control groups) at 0, 5, 15, 30 and 60 min respectively. RESULTS: (1) Compared with that at 0 min, the mean fluorescence intensity of JC-1 within the spermatozoal body and the percentage of orange-red colored spermatozoa in the experiment group were increased significantly at 5 and 15 min respectively after uPA incubation (P < 0.05). (2) The mean fluorescence intensity of JC-1 within the spermatozoal body at 15, 30 and 60 min and the percentage of orange-red colored spermatozoa at 5 and 15 min in the group were significantly higher than those in the control group (P < 0.05). CONCLUSION: uPA could increase the mitochondrial membrane potential of mouse capacitated-spermatozoa in vitro, and maintain it at a high level for a certain period of time. By enhancing sperm mitochondrial function, uPA may provide sufficient energy for capacitated-spermatozoa to increase their motility and change their motor pattern, which might be one of the therapeutic mechanisms of uPA on male infertility.
Keywords:urokinase-type plasminogen activator   spermatozoa   mitochondrial membrane potential    JC-1 fluorescent dye   mouse
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