Department of Animal Science, Oklahoma State University, Stillwater, USA.
Biol Reprod. 2012 Oct 4;87(4):79. doi: 10.1095/biolreprod.111.096735. Print 2012 Oct.
Hedgehog signaling is involved in regulation of ovarian function in Drosophila, but its role in regulating mammalian ovarian folliculogenesis is less clear. Therefore, gene expression of Indian hedgehog (IHH) and its type 1 receptor, patched 1 (PTCH1), were quantified in bovine granulosa (GC) or theca (TC) cells of small (1-5 mm) antral follicles by in situ hybridization and of larger (5-17 mm) antral follicles by real-time RT-PCR from ovaries of cyclic cows genetically selected (Twinner) or not selected (control) for twin ovulations. Expression of IHH mRNA was localized to GC and cumulus cells, whereas PTCH1 mRNA was greater in TC than in GC. Estrogen-active (E-A; follicular fluid concentration of estradiol > progesterone) versus estrogen-inactive follicles had a greater abundance of mRNA for IHH in GC and PTCH1 in TC. Abundance of IHH mRNA in GC was not affected by cow genotype, whereas TC PTCH1 mRNA was less in large E-A follicles of Twinners than in controls. In vitro, estradiol and wingless-type (WNT) 3A increased IHH mRNA in IGF1-treated GC. IGF1 and BMP4 treatments decreased PTCH1 mRNA in small TC. Estradiol and LH increased PTCH1 mRNA in IGF1-treated TC from large and small follicles, respectively. In summary, functional status of ovarian follicles was associated with differences in hedgehog signaling in GC and TC. We hypothesize that as follicles grow and develop, increased free IGF1 may suppress expression of IHH mRNA by GC and PTCH1 mRNA by TC, and these effects are regulated in a paracrine way by estradiol and other intra- and extragonadal factors.
Hedgehog 信号通路参与了果蝇卵巢功能的调控,但它在调节哺乳动物卵巢卵泡发生中的作用尚不清楚。因此,通过原位杂交技术,检测了来自具有双胎排卵遗传选择(Twinner)或无选择(对照)的循环奶牛卵巢中小(1-5mm)窦卵泡的颗粒细胞(GC)或膜细胞(TC),以及大(5-17mm)窦卵泡中印度 Hedgehog(IHH)及其 1 型受体 patched 1(PTCH1)的基因表达;通过实时 RT-PCR 检测了具有双胎排卵遗传选择(Twinner)或无选择(对照)的循环奶牛卵巢中小(1-5mm)窦卵泡和大(5-17mm)窦卵泡中 IHH 和 PTCH1 的基因表达。IHH mRNA 定位于 GC 和卵丘细胞,而 PTCH1 mRNA 在 TC 中比在 GC 中更为丰富。与雌激素不活跃(E-A;卵泡液中雌二醇浓度>孕酮)相比,雌激素活跃(E-A)卵泡的 GC 中 IHH 和 TC 中 PTCH1 的 mRNA 丰度更高。GC 中 IHH mRNA 的丰度不受奶牛基因型的影响,而大型 E-A 卵泡中 Twinner 的 TC PTCH1 mRNA 少于对照组。体外实验中,雌二醇和 wingless-type(WNT)3A 增加了 IGF1 处理的 GC 中 IHH mRNA 的表达。IGF1 和 BMP4 处理降低了小 TC 中 PTCH1 mRNA 的表达。雌二醇和 LH 分别增加了 IGF1 处理的大、小卵泡 TC 中 PTCH1 mRNA 的表达。总之,卵巢卵泡的功能状态与 GC 和 TC 中 Hedgehog 信号的差异有关。我们假设,随着卵泡的生长和发育,增加的游离 IGF1 可能会抑制 GC 中 IHH mRNA 和 TC 中 PTCH1 mRNA 的表达,而这些效应受到雌二醇和其他内外源因子的旁分泌调节。