Shahed Asha, McMichael Carling F, Young Kelly A
Reproductive Biology Group, Department of Biological Sciences, California State University Long Beach, Long Beach, California.
J Exp Zool A Ecol Genet Physiol. 2015 Nov;323(9):627-36. doi: 10.1002/jez.1953. Epub 2015 Jul 14.
This study sought to characterize the rapid intraovarian mRNA response of key folliculogenic factors that may contribute to the restoration of folliculogenesis during 2-10 days of photostimulation in Siberian hamsters. Adult hamsters were exposed to short photoperiod (8L:16D) for 14 weeks (SD). A subset were then transferred to long photoperiod (16L:8D) for 2 (PT day-2), 4 (PT day-4), or 10 days (PT day-10). Quantitative real-time PCR was used to measure intraovarian mRNA expression of: gonadotropin releasing hormone (GnRH), follicle stimulating hormone β-subunit (FSHβ-subunit), luteinizing hormone β-subunit (LHβ-subunit), FSH and LH receptors, estrogen receptors α and β (Esr1 and Esr2), matrix metalloproteinase (MMP)-2 and -9, anti-Müllerian hormone (AMH), inhibin-α subunit, fibroblast growth factor-2 (FGF-2) and proliferating cell nuclear antigen (PCNA). Compared to SD, plasma FSH concentrations increased on PT day-4 and the number of antral follicles and corpora lutea increased on PT day-10. FSHR and inhibin-α mRNA expression also increased on PT day-4, whereas LHR and proliferation marker PCNA both increased on PT day-10 as compared to SD. Esr1 mRNA increased on PT day-2 and remained significantly increased as compared to SD, whereas Esr1 mRNA increased only on PT day-2, similar to FGF-2 and MMP-2 results. No differences were observed in mRNA expression in ovarian GnRH, FSHβ- and LHβ-subunits, AMH, and MMP-9 mRNA with 2-10 days of photostimulation. Rapid increases in intraovarian FSHR and inhibin-α mRNA and antral follicle/corpora lutea numbers suggest that the ovary is primed to react quickly to the FSH released in response to brief periods of photostimulation.
本研究旨在描述关键卵泡生成因子在西伯利亚仓鼠光刺激2至10天期间卵巢内mRNA的快速反应,这些因子可能有助于卵泡生成的恢复。成年仓鼠暴露于短光照周期(8小时光照:16小时黑暗)14周(短日照组)。然后将一部分仓鼠转移至长光照周期(16小时光照:8小时黑暗)2天(转移后第2天)、4天(转移后第4天)或10天(转移后第10天)。采用定量实时PCR检测卵巢内以下基因的mRNA表达:促性腺激素释放激素(GnRH)、促卵泡激素β亚基(FSHβ亚基)、促黄体生成素β亚基(LHβ亚基)、FSH和LH受体、雌激素受体α和β(Esr1和Esr2)、基质金属蛋白酶(MMP)-2和-9、抗苗勒管激素(AMH)、抑制素α亚基、成纤维细胞生长因子-2(FGF-2)和增殖细胞核抗原(PCNA)。与短日照组相比,转移后第4天血浆FSH浓度升高,转移后第10天窦状卵泡和黄体数量增加。与短日照组相比,转移后第4天FSHR和抑制素α mRNA表达也增加,而转移后第10天LHR和增殖标志物PCNA均增加。Esr1 mRNA在转移后第2天增加,与短日照组相比仍显著升高,而Esr2 mRNA仅在转移后第2天增加,与FGF-2和MMP-2结果相似。在光刺激2至10天期间,卵巢GnRH、FSHβ和LHβ亚基、AMH和MMP-9 mRNA表达未观察到差异。卵巢内FSHR和抑制素α mRNA以及窦状卵泡/黄体数量的快速增加表明,卵巢已做好准备,对因短暂光刺激而释放的FSH做出快速反应。