Division of Obstetrics and Gynecology, National Cheng Kung University College of Medicine and Hospital, Dou-Liou Branch, Yunlin, Taiwan.
J Assist Reprod Genet. 2011 Sep;28(9):851-61. doi: 10.1007/s10815-011-9602-0. Epub 2011 Jun 24.
To understand the molecular basis of sperm-motility and to identify related novel motility biomarkers.
Two-dimensional electrophoresis (2DE) followed by Reverse-phase-nano-high-performance liquid chromatography-electrospray ionization tandem mass spectrometry (RP-nano-HPLC-ESI-MS/MS) were applied to establish the human sperm proteome. Then the sperm proteome of moderate-motile human sperm fraction and that of good-motile human sperm fraction from pooled spermatozoa of forty normozoospermic donors (Group 1 subjects) were compared to identify the dysregulated proteins. Among these down-regulated proteins, Protein tyrosine phosphatase non-receptor type 14 (PTPN14) was chosen to reconfirm by Western blotting and semi-quantitative reverse transcription polymerase chain reaction. For clinical application, Western blotting and real-time reverse transcription polymerase chain reaction was performed to compare the expression level of PTPN14 in (Group 2 subjects) nine normozoospermic controls and thirty-three asthenozoospermic patients (including 21 mild asthenozoospermic cases and 12 severe cases). Finally, bioinformatic tools prediction and immunofluorescence assay were performed to elucidate the potential localization of PTPN14.
The expression levels of three proteins were observed to be lower in the moderate-motile sperm fraction than in good-motile sperm of group 1 subjects. Among three proteins with persistent down-regulation in the moderate-motile sperm, we reconfirmed that the expression level of PTPN14 was significantly lower in both mRNA and protein levels from the moderate-motile sperm fraction. Further, down-regulation of PTPN14 was found at the translational and transcriptional level in the asthenozoospermic men. Finally, Bioinformatic tools prediction and immunofluorescence assay showed that PTPN14 maybe predominantly localized at the mitochondria in the midpiece of human ejaculated sperm.
Proteomics tools were applied to identify three possible sperm motility-related proteins. Among these proteins, PTPN14 was highly likely a novel sperm-motility biomarker and a potential mitochondrial protein.
了解精子运动的分子基础,鉴定相关的新型运动生物标志物。
采用二维电泳(2-DE)结合反相-纳米高效液相色谱-电喷雾串联质谱(RP-nano-HPLC-ESI-MS/MS)技术建立人精子蛋白质组图谱。然后将 40 位正常生育力供体的混合精子中中速运动精子部分和快速运动精子部分的精子蛋白质组图谱进行比较,以鉴定失调蛋白。在这些下调蛋白中,选择蛋白酪氨酸磷酸酶非受体型 14(PTPN14)进行 Western 印迹和半定量逆转录聚合酶链反应(RT-PCR)重新确认。为了临床应用,对 9 例正常生育力对照和 33 例弱精子症患者(包括 21 例轻度弱精子症和 12 例重度弱精子症)进行 Western 印迹和实时 RT-PCR 比较 PTPN14 的表达水平。最后,通过生物信息学工具预测和免疫荧光分析阐明 PTPN14 的潜在定位。
在第 1 组中,观察到中速运动精子部分的三种蛋白质的表达水平低于快速运动精子部分。在三种持续下调的中速运动精子蛋白中,我们重新确认了 PTPN14 的表达水平在中速运动精子部分的 mRNA 和蛋白水平均显著降低。此外,在弱精子症男性中,PTPN14 在翻译和转录水平下调。最后,生物信息学工具预测和免疫荧光分析显示,PTPN14 可能主要定位于人射出精子中段的线粒体。
蛋白质组学工具用于鉴定三种可能与精子运动相关的蛋白质。在这些蛋白中,PTPN14 很可能是一种新的精子运动生物标志物和潜在的线粒体蛋白。