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IGF-1受体信号通路以及AMPK激活对母鸡颗粒细胞中IGF-1诱导的孕酮分泌的影响。

IGF-1 receptor signaling pathways and effects of AMPK activation on IGF-1-induced progesterone secretion in hen granulosa cells.

作者信息

Tosca Lucie, Chabrolle Christine, Crochet Sabine, Tesseraud Sophie, Dupont Joëlle

机构信息

INRA, UMR 6175, Unité de physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France.

出版信息

Domest Anim Endocrinol. 2008 Feb;34(2):204-16. doi: 10.1016/j.domaniend.2007.03.001. Epub 2007 Apr 9.

Abstract

IGF-1 plays a key role in the proliferation and differentiation of granulosa cells. However, the molecular mechanism of IGF-1 action in avian granulosa cells during follicle maturation is unclear. Here, we first studied IGF-1 receptor (IGF-1R) expression, IGF-1-induced progesterone production and some IGF-1R signaling pathways in granulosa cells from different follicles. IGF-1R (mRNA and protein) was higher in fresh or cultured granulosa cells from the largest follicles (F1 or F2) than in those from smaller follicles (F3 or F4). In vitro, IGF-1 treatment (10(-8)M, 36h) increased progesterone secretion by four-fold in mixed F3 and F4 (F3/4) granulosa cells and by 1.5-fold in F1 granulosa cells. IGF-1 (10(-8)M, 30min)-induced increases in tyrosine phosphorylation of IGF-1R beta subunit and phosphorylation of ERK were higher in F1 than in F3/4 granulosa cells. Interestingly, IGF-1 stimulation (10(-8)M, 10min) decreased the level of AMPK Thr172 phosphorylation in F1 and F3/4 granulosa cells. We have recently showed that AMPK (AMP-activated protein kinase) is a protein kinase involved in the steroidogenesis in chicken granulosa cells. We then studied the effects of AMPK activation by AICAR (5-aminoimidazole-4-carboxamide ribonucleoside), an activator of AMPK, on IGF-1-induced progesterone secretion by F3/4 and F1 granulosa cells. AICAR treatment (1mM, 36h) increased IGF-1-induced progesterone secretion, StAR protein levels and decreased ERK phosphorylation in F1 granulosa cells. Opposite data were observed in F3/4 granulosa cells. Adenovirus-mediated expression of dominant negative AMPK totally reversed the effects of AICAR on IGF-1-induced progesterone secretion, StAR protein production and ERK phosphorylation in both F3/4 and F1 granulosa cells. Thus, a variation of energy metabolism through AMPK activation could modulate differently IGF-1-induced progesterone production in F1 and F3/4 granulosa cells.

摘要

胰岛素样生长因子-1(IGF-1)在颗粒细胞的增殖和分化中起关键作用。然而,在卵泡成熟过程中IGF-1作用于禽类颗粒细胞的分子机制尚不清楚。在此,我们首先研究了不同卵泡颗粒细胞中IGF-1受体(IGF-1R)的表达、IGF-1诱导的孕酮产生以及一些IGF-1R信号通路。来自最大卵泡(F1或F2)的新鲜或培养颗粒细胞中的IGF-1R(mRNA和蛋白质)水平高于来自较小卵泡(F3或F4)的颗粒细胞。在体外,IGF-1处理(10^(-8)M,36小时)使混合的F3和F4(F3/4)颗粒细胞中的孕酮分泌增加了四倍,使F1颗粒细胞中的孕酮分泌增加了1.5倍。IGF-1(10^(-8)M,30分钟)诱导的IGF-1Rβ亚基酪氨酸磷酸化增加和ERK磷酸化在F1颗粒细胞中高于F3/4颗粒细胞。有趣的是,IGF-1刺激(10^(-8)M,10分钟)降低了F1和F3/4颗粒细胞中AMPK Thr172的磷酸化水平。我们最近发现,AMPK(AMP激活的蛋白激酶)是一种参与鸡颗粒细胞类固醇生成的蛋白激酶。然后,我们研究了AMPK激活剂AICAR(5-氨基咪唑-4-甲酰胺核苷)激活AMPK对F3/4和F1颗粒细胞中IGF-1诱导的孕酮分泌的影响。AICAR处理(1mM,36小时)增加了IGF-1诱导的孕酮分泌、类固醇生成急性调节蛋白(StAR)蛋白水平,并降低了F1颗粒细胞中的ERK磷酸化。在F3/4颗粒细胞中观察到相反的数据。腺病毒介导的显性负性AMPK表达完全逆转了AICAR对F3/4和F1颗粒细胞中IGF-1诱导的孕酮分泌、StAR蛋白产生和ERK磷酸化的影响。因此,通过激活AMPK引起的能量代谢变化可能对F1和F3/4颗粒细胞中IGF-1诱导的孕酮产生产生不同的调节作用。

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