Luo Bin, He Wei, Wang Shi-Heng, Xiong Hong-Ping, Liang Xin, Shan Xu-Dong, Lü Zi-Li
Center of Reproductive Medicine; The Second Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610041, China.
Department of Clinical Laboratory, The Second Affiliated Hospital of Chengdu University of Traditional Chinese Medicine, Chengdu, Sichuan 610041, China.
Zhonghua Nan Ke Xue. 2017 Nov;23(11):1002-1006.
To investigate the mRNA and protein expressions of outer dense fiber 2 (ODF2) in the sperm of the asthenospermia patient and their differences from those in normal healthy men.
According to the WHO criteria, we collected semen samples from 45 asthenozoospermia patients and 15 normal healthy volunteers. Using computer-assisted sperm analysis (CASA), we divided the semen samples from the asthenospermia patients into a mild, a moderate and a severe group, and determined the mRNA and protein expressions of ODF2 in different groups by RT-PCR and Western blot.
Compared with the normal healthy men, the expression of the ODF2 gene showed no statistically significant difference in the mild asthenospermia group (1.112 0 ± 0.525 5 vs 0.688 0 ± 0.372 0, P >0.05) but remarkably decreased in the moderate (0.483 3 ± 0.186 3, P <0.05) and severe asthenospermia patients (0.448 3 ± 0.340 8, P <0.01). The OD value (ODF2/β-actin) of the ODF2 protein in the normal men exhibited no statistically significant difference from that in the mild asthenospermia group (0.458 7 ± 0.052 1 vs 0.326 1 ± 0.071 4, P >0.05), but markedly lower than in the moderate (0.145 4 ± 0.053 6, P <0.05) and severe asthenospermia patients (0.122 7 ± 0.045 7, P <0.01), which was consistent with the results of RT-PCR.
Decreased mRNA and protein expressions of ODF2 in the sperm are positively correlated with declined sperm motility of the asthenospermia patient, which is suggestive of the involvement of the ODF2 gene in the regulation of sperm motility.
研究弱精子症患者精子中外周致密纤维蛋白2(ODF2)的mRNA和蛋白表达情况,以及与正常健康男性的差异。
按照世界卫生组织标准,收集45例弱精子症患者和15例正常健康志愿者的精液样本。采用计算机辅助精子分析(CASA),将弱精子症患者的精液样本分为轻度、中度和重度组,通过RT-PCR和Western blot检测不同组中ODF2的mRNA和蛋白表达。
与正常健康男性相比,轻度弱精子症组ODF2基因表达差异无统计学意义(1.112 0±0.525 5 vs 0.688 0±0.372 0,P>0.05),中度(0.483 3±0.186 3,P<0.05)和重度弱精子症患者(0.448 3±0.340 8,P<0.01)中ODF2基因表达显著降低。正常男性ODF2蛋白的OD值(ODF2/β-肌动蛋白)与轻度弱精子症组差异无统计学意义(0.458 7±0.052 1 vs 0.326 1±0.071 4,P>0.05),但明显低于中度(0.145 4±0.053 6,P<0.05)和重度弱精子症患者(0.122 7±0.045 7,P<0.01),这与RT-PCR结果一致。
精子中ODF2的mRNA和蛋白表达降低与弱精子症患者精子活力下降呈正相关,提示ODF2基因参与精子活力的调控。