Bahmanpour Soghra, Talaei Khozani Tahereh, Zarei Fard Nehleh, Jaberipour Mansoureh, Hosseini Ahmah, Esmaeilpour Tahereh
Laboratory for Stem Cell Research, Department of Anatomy, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Institute Cancer Research, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Iran J Reprod Med. 2013 Oct;11(10):815-22.
The interaction between follicular cells and oocyte leads to a change in gene expression involved in oocyte maturation processes.
The purpose of this study was to quantify the expression of more common genes involved in follicular growth and oocyte developmental competence.
In this experimental study, the expression of genes was evaluated with qRT-PCR assay in female BALB/c mice pups at 3-day of pre-pubertal and 8 week old virgin adult ovaries. The tissue was prepared by H&E staining for normal morphological appearance. The data were calculated with the 2-∆Ct formula and assessed using non-parametric two-tailed Mann-Whitney test. The p<0.05 was considered as significant.
The data showed a significant increase in the level of Stra8 and GDF9 in adult compared with newborn mice ovaries (p=0.049). In contrast, a significant decrease in the level of Mvh, REC8, SCP1, SCP3, and ZP2 was observed in adult mice ovaries compared to those in the newborn mice ovaries (all p=0.049 except SCP1: p=0.046). There was no significant difference in the level of OCT4 and Cx37 expression between adult and newborn mice ovaries.
The modifications in gene expression patterns coordinate the follicular developmental processes. Furthermore, the findings showed higher expression level of premeiotic gene (Stra8) and lower level of meiotic entry markers (SCP1, SCP3, and REC8) in juvenile than newborn mouse ovaries. This article extracted from Ph.D. thesis. (Nehleh Zarei fard).
卵泡细胞与卵母细胞之间的相互作用导致参与卵母细胞成熟过程的基因表达发生变化。
本研究旨在量化参与卵泡生长和卵母细胞发育能力的更常见基因的表达。
在本实验研究中,通过qRT-PCR检测法评估雌性BALB/c幼鼠在青春期前3天和8周龄未交配成年小鼠卵巢中基因的表达。通过苏木精-伊红染色制备组织以观察正常形态。数据采用2-∆Ct公式计算,并使用非参数双尾曼-惠特尼检验进行评估。p<0.05被认为具有统计学意义。
数据显示,与新生小鼠卵巢相比,成年小鼠卵巢中Stra8和GDF9水平显著升高(p=0.049)。相反,与新生小鼠卵巢相比,成年小鼠卵巢中Mvh、REC8、SCP1、SCP3和ZP2水平显著降低(除SCP1:p=0.046外,其余均为p=0.049)。成年小鼠和新生小鼠卵巢中OCT4和Cx37表达水平无显著差异。
基因表达模式的改变协调了卵泡发育过程。此外,研究结果显示,幼年小鼠卵巢中减数分裂前基因(Stra8)的表达水平高于新生小鼠卵巢,而减数分裂进入标记物(SCP1、SCP3和REC8)的水平低于新生小鼠卵巢。本文摘自博士论文(Nehleh Zarei fard)。