Ambulkar Prafulla S, Waghmare Jwalant E, Chaudhari Ajay R, Wankhede Vandana R, Tarnekar Aaditya M, Shende Moreshwar R, Pal Asoke K
Senior Research Fellow and Department of Anatomy, Human Genetic Division, Mahatma Gandhi Institute of Medical Sciences , Sevagram, Wardha, Maharashtra, India .
Associate Professor, Department of Anatomy, Mahatma Gandhi Institute of Medical Sciences , Sevagram, Wardha, Maharashtra, India .
J Clin Diagn Res. 2016 Nov;10(11):GC09-GC12. doi: 10.7860/JCDR/2016/22412.8843. Epub 2016 Nov 1.
Mitochondria and mitochondrial DNA are essential to sperm motility and fertility. It controls growth, development and differentiation through oxidation energy supply. Mitochondrial (mtDNA) deletions or mutation are frequently attributed to defects of sperm motility and finally these deletions lead to sperm dysfunction and causes infertility in male.
To investigate the correlation between large scale 7436-bp deletions in sperm mtDNA and non-motility of sperm in asthenozoospermia and Oligoasthenoteratozoospermia (OAT) infertile men.
The present prospective study was carried out in Human Genetic Division, Department of Anatomy, Mahatma Gandhi Institute of Medical Sciences, Sevagram from June 2014 to July 2016. We have studied 110 asthenozoospermia and OAT infertile men whose semen profile indicated abnormal motility and 50 normal fertile controls. Of 110 infertile men, 70 had asthenozoospermia and 40 had OAT. Fractionations of spermatozoa were done in each semen sample on the basis of their motility by percoll gradients discontinuous technique. Long-range PCR was used for detection of 7436-bp deletions in sperm mtDNA and was confirmed by primer shift technique.
Overall eight subjects (8/110; 7.2%) of which six (6/70; 8.57%) asthenozoospermia and two (2/40; 5%) OAT had shown deletions of 7436-bp. In 40% percoll fraction had more non-motile spermatozoa than 80% percoll fraction. The non-motile spermatozoa in 40% percoll fractions showed more mtDNA deletions (7.2%) than the motile spermatozoa in 80% percoll fraction (2.7%). The sequencing of flanking regions of deleted mtDNA confirmed 7436-bp deletions. Interestingly, no deletions were found in control subjects.
Though, the frequency of 7436-bp deletions in sperm mtDNA was low in infertile cases but meaningful indications were there when results were compared with controls. It is indicated that large scale deletions 7436-bp of mtDNA is associated with abnormal sperm motility. The 7436-bp deletions of mtDNA in spermatozoa may be one of the important causes of dysfunction and non-motile sperm.
线粒体和线粒体DNA对精子活力和生育能力至关重要。它通过氧化能量供应来控制生长、发育和分化。线粒体(mtDNA)缺失或突变常被认为与精子活力缺陷有关,最终这些缺失会导致精子功能障碍并引起男性不育。
研究弱精子症和少弱畸精子症(OAT)不育男性精子mtDNA中7436-bp大片段缺失与精子不动之间的相关性。
本前瞻性研究于2014年6月至2016年7月在塞格拉姆市圣雄甘地医学科学研究所解剖学系人类遗传学部门进行。我们研究了110例弱精子症和OAT不育男性,其精液分析显示精子活力异常,以及50例正常生育对照者。在110例不育男性中,70例为弱精子症,40例为OAT。通过不连续 Percoll 梯度技术,根据精子活力对每个精液样本中的精子进行分级分离。采用长距离PCR检测精子mtDNA中的7436-bp缺失,并通过引物移位技术进行确认。
总体上有8名受试者(8/110;7.2%),其中6名弱精子症患者(6/70;8.57%)和2名OAT患者(2/40;5%)出现了7436-bp的缺失。在40%Percoll分级中的无活力精子比80%Percoll分级中的更多。40%Percoll分级中的无活力精子显示出比80%Percoll分级中的有活力精子更多的mtDNA缺失(7.2%对2.7%)。对缺失mtDNA侧翼区域的测序证实了7436-bp的缺失。有趣的是,在对照受试者中未发现缺失。
虽然不育病例中精子mtDNA中7436-bp缺失的频率较低,但与对照组相比结果时有有意义的迹象。表明mtDNA的7436-bp大片段缺失与精子活力异常有关。精子中mtDNA的7436-bp缺失可能是精子功能障碍和无活力的重要原因之一。