Sepideh Jabbari, Reza Sadeghi Mohammad, Mahdi Akhondi Mohammad, Azadeh Ebrahim Habibi, Naser Amirjanati, Niknam Lakpour, Lima Asgharpour, Ardekani Ali M
Department of Biology, Islamic Azad University, Science and Research Branch, Tehran, Iran.
J Reprod Infertil. 2009 Oct;10(3):185-91.
In mammalian system, spermatozoa are not able to fertilize the oocyte immediately upon ejaculation, thus they undergo a series of biochemical and molecular changes which is termed capacitation. During sperm capacitation, signal transduction pathways are activated which lead to protein tyrosine phosphorylation. Tyrosine phosphorylated proteins have an important role in sperm capacitation such as hyperactive motility, interaction with zona pellucida and acrosome reaction. Evaluation of tyrosine phosphorylation pattern is important for further understanding of molecular mechanisms of fertilization and the etiology of sperm dysfunctions and abnormalities such as teratospermia. The goal of this study is to characterize tyrosine phosphorylation pattern in sperm proteins isolated from normospermic and teratospermic infertile men attending Avicenna Infertility Clinic in Tehran.
Semen samples were collected and the spermatozoa were isolated using Percoll gradient centrifugation. Then the spermatozoa were incubated up to 6h at 37°C with 5% CO2 in 3% Bovine Serum Albumin-supplemented Ham's F-10 for capacitation to take place. The total proteins from spermatozoa were extracted and were subjected to SDS-PAGE before and after capacitation. To evaluate protein tyrosine phosphorylation pattern, western blotting with specific antibody against phosphorylated tyrosines was performed.
THE RESULTS UPON WESTERN BLOTTING SHOWED: 1) at least six protein bands were detected before capacitation in the spermatozoa from normospermic samples. However, comparable levels of tyrosine phosphorylation was not observed in the spermatozoa from teratospermic samples. 2) The intensity of protein tyrosine phosphorylation appears to have been increased during capacitation in the normospermic relative to the teratospermic group.
For the first time, these findings demonstrate and suggest that the differences in the types of proteins and diminished tyrosine phosphorylation efficiency in sperm from teratospermic men may be responsible for their compromised capacitation and low fertilization success rates.
在哺乳动物系统中,精子在射精后不能立即使卵母细胞受精,因此它们会经历一系列生化和分子变化,这一过程被称为获能。在精子获能过程中,信号转导通路被激活,导致蛋白质酪氨酸磷酸化。酪氨酸磷酸化蛋白在精子获能中具有重要作用,如活跃的运动能力、与透明带的相互作用以及顶体反应。评估酪氨酸磷酸化模式对于进一步理解受精的分子机制以及精子功能障碍和异常(如畸形精子症)的病因很重要。本研究的目的是表征从德黑兰阿维森纳不孕诊所就诊的正常精子症和畸形精子症不育男性中分离出的精子蛋白中的酪氨酸磷酸化模式。
收集精液样本,使用Percoll梯度离心法分离精子。然后将精子在37°C、5%二氧化碳的条件下,于添加3%牛血清白蛋白的Ham's F-10培养基中孵育6小时,使其发生获能。提取精子的总蛋白,并在获能前后进行SDS-PAGE。为了评估蛋白质酪氨酸磷酸化模式,使用针对磷酸化酪氨酸的特异性抗体进行蛋白质印迹分析。
蛋白质印迹分析结果显示:1)在正常精子样本的精子获能前检测到至少六条蛋白条带。然而,在畸形精子样本的精子中未观察到类似水平的酪氨酸磷酸化。2)与畸形精子组相比,正常精子组在获能过程中蛋白质酪氨酸磷酸化的强度似乎有所增加。
这些发现首次证明并表明,畸形精子症男性精子中蛋白质类型的差异和酪氨酸磷酸化效率的降低可能是其获能受损和受精成功率低的原因。