Center for Reproductive Biology and Health, and the Department of Animal Science, The Pennsylvania State University, University Park, PA 16802, USA.
Poult Sci. 2018 Oct 1;97(10):3755-3761. doi: 10.3382/ps/pey224.
Similar to the domestic hen ovary, entry of a follicle into the preovulatory hierarchy in the turkey hen represents a process in which a single follicle initiates rapid growth and final maturation prior to ovulation. Published data derived from the laying hen support the proposal that differentiation of the follicle granulosa cell (GC) layer begins coincident with entry into the rapid growth phase and is characterized by the initial capacity for follicle stimulating hormone (FSH)-mediated cell signaling. The present studies were conducted with photostimulated B.U.T. Big 6 turkey hens to compare follicle dynamics and cellular mechanisms to those in the laying hen. The measurement and weights of turkey ovarian follicles greater than 1 mm in diameter revealed a discrete size hierarchy that was maintained throughout follicle development. GC layers collected from the single follicle initiating rapid growth (at the 11 to 13 mm stage of development) and incubated, in vitro, for 3 h with recombinant human (rh) FSH (10 ng/mL) responded with significantly increased steroidogenic acute regulatory protein (STAR) mRNA expression and progesterone production. The same treatment induced minimal STAR expression and no significant progesterone accumulation in GCs from 8 to 9 mm follicles (prior to the rapid growth phase). By comparison, dispersed GCs from 8 to 9 mm follicles pre-cultured for 18 h followed by a 3 h challenge with rhFSH resulted in significantly increased STAR expression plus progesterone production. Significantly, such cultured GCs pretreated for 15 min with transforming growth factor alpha (TGFα; 10 ng/mL) completely prevented both rhFSH-induced STAR expression and progesterone production. Culture of GCs from 8 to 9 mm follicles for 21 h with Bone Morphogenetic Protein 6 (BMP6) increased both cholesterol side-chain cleavage enzyme (CYP11A1) and FSH receptor mRNA (FSHR) expression. BMP6 also enhanced rhFSH-induced STAR expression, and this effect was blocked by TGFα. Collectively, these results support a conservation of mechanisms that maintain a hierarchy of follicles throughout development plus initiate FSH-responsiveness and GC differentiation as the recruited follicle enters the rapid growth phase in these closely related species.
类似于国内母鸡的卵巢,火鸡母鸡的卵泡进入预排卵等级代表了一个过程,即单个卵泡在排卵前开始快速生长和最终成熟。来自产蛋母鸡的已发表数据支持这样的提议,即卵泡颗粒细胞 (GC) 层的分化始于进入快速生长阶段,并以初始卵泡刺激素 (FSH) 介导的细胞信号传导能力为特征。本研究使用光刺激的 B.U.T. Big 6 火鸡母鸡进行,以比较卵泡动力学和细胞机制与产蛋母鸡的卵泡动力学和细胞机制。大于 1 毫米直径的火鸡卵巢卵泡的测量和重量显示出一个离散的大小等级,在整个卵泡发育过程中保持不变。从开始快速生长的单个卵泡(在发育的 11 到 13 毫米阶段)中收集的 GC 层,在体外与重组人 (rh) FSH(10ng/mL)孵育 3 小时,类固醇生成急性调节蛋白 (STAR) mRNA 表达和孕酮产生显著增加。相同的处理在 8 到 9 毫米卵泡(快速生长阶段之前)的 GC 中诱导最小的 STAR 表达和无显著孕酮积累。相比之下,预先培养 18 小时的 8 到 9 毫米卵泡的分散 GC,然后用 rhFSH 进行 3 小时的挑战,导致 STAR 表达加上孕酮产生显著增加。重要的是,预处理 15 分钟的转化生长因子 alpha (TGFα;10ng/mL) 完全阻止了 rhFSH 诱导的 STAR 表达和孕酮产生。用骨形态发生蛋白 6 (BMP6) 培养 8 到 9 毫米卵泡的 GC 21 小时,增加了胆固醇侧链裂解酶 (CYP11A1) 和 FSH 受体 mRNA (FSHR) 的表达。BMP6 还增强了 rhFSH 诱导的 STAR 表达,这种作用被 TGFα 阻断。总的来说,这些结果支持了在这些密切相关的物种中,维持卵泡等级的机制以及启动 FSH 反应性和 GC 分化的机制的保守性,因为被募集的卵泡进入快速生长阶段。