Tosca Lucie, Chabrolle Christine, Crochet Sabine, Tesseraud Sophie, Dupont Joëlle
INRA, UMR 6175, Unité de physiologie de la Reproduction et des Comportements, 37380 Nouzilly, France.
Domest Anim Endocrinol. 2008 Feb;34(2):204-16. doi: 10.1016/j.domaniend.2007.03.001. Epub 2007 Apr 9.
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.
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。