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iTRAQ-based analysis of sperm proteome from normozoospermic men achieving the rescue-ICSI pregnancy after the IVF failure
Authors:Xin Liu  Gensheng Liu  Juan Liu  Peng Zhu  Jiahui Wang  Yanwei Wang  Wenting Wang  Ning Li  Xuebo Wang  Chenglin Zhang  Xiaofang Shen  Fujun Liu
Affiliation:1.Central Laboratory,The Affiliated Yantai Yuhuangding Hospital of Qingdao University,Yantai,People’s Republic of China;2.Reproductive Center,Tianjin Aiwei Hospital,Tianjin,People’s Republic of China;3.Department of Clinical Laboratory,The Affiliated Yantai Yuhuangding Hospital of Qingdao University,Yantai,People’s Republic of China;4.Reproductive Center,Beijing BaoDao Obstetrics and Gynecology Hospital,Beijing,People’s Republic of China
Abstract:

Background

In the assisted reproduction, the infertile molecules of spermatozoa from normozoospermic men who underwent the unexplained failure of in vitro fertilization (IVF) due to the lack of sperm binding to the normal zona pellucida, and then achieved pregnancy with the rescue intracytoplasmic sperm injection (R-ICSI) remain unclear. More works are still necessary to explore this male infertile mechanism.

Methods

Normozoospermicmen with the IVF pregnancy and normozoospermic men with the R-ICSI pregnancy after the conventional IVF failure were collected. iTRAQ-based proteomic approach were performed to reveal the new infertile causes between the IVF pregnancy men and the R-ICSI pregnancy men. To validate the confidence of proteome data, the individual samples were analyzed by western blot and immunofluorescence. Further, the spontaneous acrosome reactions were measured to evaluate the sperm quality.

Results

Compared with IVF pregnancy group, 56 sperm proteins were differentially expressed in the R-ICSI pregnancy group. Bioinformatic analyses (PANTHER, DAVID, PubMed and STRING) indicated these altered sperm proteins were involved in various molecular functions: reproduction, chromosome organization, and sperm-oocyte interaction. Moreover, the confidence of proteome data was confirmed by western blot and immunofluorescence using the individual samples, which were consistent with our proteomic data. Additionally, an increased rate of the spontaneous acrosome reaction rate was found in the R-ICSI pregnancy group.

Conclusions

The sealtered sperm proteins and the increased spontaneous acrosome reaction rate might account for this unexplained male infertility in the R-ICSI pregnancy patients. The present proteomic results will throw light on the better understanding of the unexplained infertile mechanisms underlying these normozoospermic man who achieved R-ICSI pregnancy after IVF failure.
Keywords:
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