Sakurada Yosuke, Shirota Mariko, Inoue Kaoru, Uchida Naohiro, Shirota Kinji
Research Institute of Biosciences and High-Tech Research Center, Azabu University, 1-17-71 Fuchinobe, Sagamihara, Kanagawa 2298501, Japan.
Histochem Cell Biol. 2006 Dec;126(6):735-41. doi: 10.1007/s00418-006-0205-2. Epub 2006 Jun 13.
The recently developed laser microdissection (LMD) technique makes it possible to quantify local gene expression in the target cells of various tissues. Using the LMD technique, this study aimed at comparing the amounts of mRNAs encoding the inhibin-alpha subunit and cytochrome P450 aromatase (P450(arom)) in granulosa cells between preantral and antral follicles in immature rat ovaries. Serial frozen sections of the ovaries from 24-day-old female Wistar rats were made and 30 healthy preantral (100-200 microm maximum diameter) and ten healthy antral ( > 300 microm maximum diameter) follicles were selected in each ovary based on morphological examinations, including immunohistochemistry for inhibin-alpha, in sections adjacent to those used for LMD. The amounts of mRNAs encoding inhibin-alpha subunit and P450(arom) were quantified by real-time polymerase chain reaction (PCR). While the amount of P450(arom) mRNA in the granulosa cell layers from the antral follicles was about 12-times higher than that in the preantral follicles, no difference in the amount of inhibin-alpha mRNA was found between these two types of follicles. Thus, the LMD technique allowed the in situ quantification of gene expression in the ovary and revealed that each granulosa cell expresses a stable amount of inhibin-alpha subunit mRNA independently of antral formation in immature rat ovaries.
最近开发的激光显微切割(LMD)技术使定量分析各种组织靶细胞中的局部基因表达成为可能。本研究使用LMD技术,旨在比较未成熟大鼠卵巢中窦前卵泡和窦状卵泡颗粒细胞中抑制素α亚基和细胞色素P450芳香化酶(P450(arom))编码mRNA的含量。对24日龄雌性Wistar大鼠的卵巢制作连续冰冻切片,并基于形态学检查,包括对与用于LMD的切片相邻的切片进行抑制素α免疫组织化学,在每个卵巢中选择30个健康的窦前卵泡(最大直径100 - 200微米)和10个健康的窦状卵泡(最大直径> 300微米)。通过实时聚合酶链反应(PCR)定量抑制素α亚基和P450(arom)编码mRNA的含量。虽然窦状卵泡颗粒细胞层中P450(arom) mRNA的含量比窦前卵泡中的高约12倍,但在这两种类型的卵泡之间未发现抑制素α mRNA含量的差异。因此,LMD技术能够对卵巢中的基因表达进行原位定量,并揭示在未成熟大鼠卵巢中,每个颗粒细胞独立于卵泡腔形成表达稳定量的抑制素α亚基mRNA。