Kao Shu-Huei, Chao Hsiang-Tai, Liu Hwan-Wun, Liao Tien-Lin, Wei Yau-Huei
Department of Obstetrics and Gynecology, Taipei Veterans General Hospital, Taipei, Taiwan.
Fertil Steril. 2004 Jul;82(1):66-73. doi: 10.1016/j.fertnstert.2003.11.056.
To determine the content of sperm mitochondrial DNA (mtDNA) in patients with asthenospermia or with poor sperm motility.
Analysis of the content of mtDNA as the ratio between the amount of mtDNA and nuclear DNA by using a new concurrent polymerase chain reaction.
University hospital infertility center.
PATIENT(S): Eighty-six men who sought infertility therapy.
INTERVENTION(S): Moving characteristics of sperm were examined with a computer-assisted semen analyzer.
MAIN OUTCOME MEASURE(S): Sperm samples were classified into two groups, one with asthenospermia and the other with normal moving characteristics. The content of mtDNA in sperm was determined by polymerase chain reaction. We analyzed the mitochondrial mass by MitoTracker Green staining and analyzed DNA content with propidium iodide staining by flow cytometry.
RESULT(S): A decrease in sperm mtDNA content was detected in patients with asthenospermia or with poor sperm motility (<20% motility). The relative mtDNA contents in the asthenospermia and normal groups were 7.2 +/- 1.3 (mean +/- SD, n = 23) and 74.1 +/- 2.0 (n = 29), respectively. Lower intensities of propidium iodide staining were detected in patients with asthenospermia or poor motility, but there was no significant difference in MitoTracker Green staining between the sperm with different motility.
CONCLUSION(S): We suggest that mtDNA content may serve as a useful indicator of sperm quality and that mtDNA depletion may play an important role in the pathophysiology of some male infertility.
测定弱精子症或精子活力差患者精子线粒体DNA(mtDNA)的含量。
采用新型同步聚合酶链反应分析mtDNA含量,即mtDNA与核DNA含量之比。
大学医院不孕不育中心。
86名寻求不孕不育治疗的男性。
使用计算机辅助精液分析仪检测精子的运动特征。
将精子样本分为两组,一组为弱精子症,另一组为运动特征正常。通过聚合酶链反应测定精子中mtDNA的含量。我们用MitoTracker Green染色分析线粒体质量,并用碘化丙啶染色通过流式细胞术分析DNA含量。
在弱精子症或精子活力差(活力<20%)的患者中检测到精子mtDNA含量降低。弱精子症组和正常组的相对mtDNA含量分别为7.2±1.3(平均值±标准差,n = 23)和74.1±2.0(n = 29)。在弱精子症或活力差的患者中检测到较低强度的碘化丙啶染色,但不同活力精子之间的MitoTracker Green染色没有显著差异。
我们认为mtDNA含量可能是精子质量的一个有用指标,并且mtDNA耗竭可能在某些男性不育的病理生理学中起重要作用。