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Lanosterol 14alpha-demethylase expression in the mouse ovary and its participation in cumulus-enclosed oocyte spontaneous meiotic maturation in vitro

机译:羊毛甾醇14α-脱甲基酶在小鼠卵巢中的表达及其参与卵丘封闭卵母细胞自发减数分裂成熟的作用

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The expression of lanosterol 14alpha-demethylase (LDM) in the mouse ovary after gonadotrophin administration was examined and the action of follicle fluid meiosis activating sterol (FF-MAS), derived from lanosterol by the action of LDM, on oocyte spontaneous maturation was also evaluated in cumulus cell enclosed oocytes (CEOs). Expression of LDM was primarily in oocytes in primordial and secondary follicles prior to administration of gonadotrophins, but obvious LDM expression was apparent in ovarian somatic cells 48 h after administration of equine chorionic gonadotrophin (eCG), especially in luteal and cumulus cells 54 h after eCG or 48 h after eCG plus 6 h after human chorionic gonadotrophin (hCG). The LDM expression in oocytes was only slightly elevated in larger growing follicles after eCG treatment. On the contrary, 48 h after hCG treatment, the elevated expression of LDM was only detected in interstitial cells. Therefore, eCG may be the primary gonadotrophin for LDM expression, and furthermore for production of FF-MAS in mouse cumulus cells (which are indispensable for oocyte maturation in vivo). Conversely, inhibitors of LDM, either 40 microM azalanstat or 50 microM RS-21745, significantly inhibited oocyte germinal vesicle breakdown (GVB) after 4h of in vitro culture; GVB rates decreased to 14 or 20%, compared to 90% in spontaneous maturation, respectively. There was no significant increase in GVB in CEOs following specific inhibitor of sterol Delta14-reductase and Delta7-reductase, AY9944-A-7 (5-100 microM), until marked oocytes degeneration appeared (50 microM). The phenomena may be ascribed to slow, passive accumulation of FF-MAS by AY9944-A-7, which cannot be associated with fast spontaneous progression. Furthermore, in spontaneous-matured CEOs, LDM was expressed preferentially in cumulus cells instead of oocytes. Therefore, FF-MAS may have a positive role in the spontaneous maturation of CEOs. In conclusion, there was an eCG-dependent dual LDM expression pattern on both oocytes and somatic cells in growing follicles in vivo, which may increase LDM expression and FF-MAS production in cumulus cells for oocyte maturation. For the first time, the inhibitory effect of LDM inhibitors on spontaneous maturation, together with the strong LDM expression in spontaneous matured CEOs, indicated that FF-MAS produced by cumulus cells might participate in spontaneous maturation of mouse CEOs.
机译:检查了促性腺激素给药后小鼠卵巢中羊毛甾醇14α-脱甲基酶(LDM)的表达,并评估了通过LDM作用衍生自羊毛甾醇的卵泡液减数分裂活化固醇(FF-MAS)对卵母细胞自然成熟的作用。在卵丘细胞封闭的卵母细胞(CEO)中。 LDM的表达主要在促性腺激素给药前的原始卵和次级卵泡中的卵母细胞中表达,但是在给予马绒毛膜促性腺激素(eCG)48小时后的卵巢体细胞中,尤其是在eCG产生54 h的黄体和卵丘细胞中,LDM表达明显或eCG后48小时加上人绒毛膜促性腺激素(hCG)后6小时。 eCG处理后,卵母细胞中LDM的表达在较大的生长卵泡中仅略有升高。相反,在hCG处理后48小时,仅在间质细胞中检测到LDM表达升高。因此,eCG可能是LDM表达的主要促性腺激素,并且可能是在小鼠卵丘细胞(体内卵母细胞成熟必不可少)中产生FF-MAS的主要促性腺激素。相反,LDM抑制剂,无论是40 microM的azalanstat还是50 microM的RS-21745,在体外培养4h后均能显着抑制卵母细胞生小囊泡分解(GVB)。 GVB率下降至14%或20%,而自然成熟时分别为90%。固醇Delta14-还原酶和Delta7-还原酶的特定抑制剂AY9944-A-7(5-100 microM)后,CEO的GVB没有显着增加,直到出现明显的卵母细胞变性(50 microM)。这种现象可能归因于AY9944-A-7对FF-MAS的缓慢,被动积累,而这与快速的自发进展无关。此外,在自发成熟的CEO中,LDM优先在卵丘细胞而不是卵母细胞中表达。因此,FF-MAS可能在CEO的自然成长中发挥积极作用。总之,在体内生长的卵泡中,卵母细胞和体细胞上均存在依赖eCG的双重LDM表达模式,这可能会增加卵母细胞成熟的卵丘细胞中LDM表达和FF-MAS产生。 LDM抑制剂对自发成熟的抑制作用,以及在自发成熟的CEO中强烈的LDM表达,首次表明,卵丘细胞产生的FF-MAS可能参与了小鼠CEO的自发成熟。

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