Chabrolle Christine, Tosca Lucie, Dupont Joélle
Unité de Physiologie de la Reproduction et des Comportements, Institut National de la Recherche Agronomique, 37380 Nouzilly, France.
Reproduction. 2007 Apr;133(4):719-31. doi: 10.1530/REP-06-0244.
In mammals, adiponectin and its receptors (AdipoR1 and AdipoR2) mRNAs are expressed in various tissues. However, the cellular expression and the role of adiponectin system have never been investigated in rat ovary. Here, we report the presence of adiponectin, AdipoR1 and AdipoR2 in rat ovaries, and we have investigated its role in granulosa cells. Using RT-PCR and western blot, we show that the mRNAs and proteins for adiponectin, AdipoR1 and AdipoR2 are found in the ovaries. Immunohistochemistry localized adiponectin, AdipoR1 and AdipoR2 in theca-interstitial T-I cells, corpus luteum, oocyte and less abundantly in granulosa cells. In the KGN human granulosa cell line, adiponectin mRNA and protein were undetectable; AdipoR2 was weakly expressed, whereas AdipoR1 was clearly present. Human chorionic gonadotrophin (hCG) injection (48 h) after pregnant mare serum gonadotrophin (PMSG) injection (24 h) in immature rats increased the level of adiponectin (protein) by about threefold (P < 0.05) and those of AdipoR1 by threefold (mRNA, P < 0.05) and 1.5-fold (protein, P < 0.05) in ovary, whereas the mRNA and protein levels of AdipoR2 were unchanged. Interestingly, hCG injection (48 h) after the PMSG treatment (24 h) decreased plasma adiponectin levels and increased insulin plasma levels. In vitro in primary rat granulosa cells, human adiponectin recombinant (5 microg/ml) in the presence or absence of follicle-stimulating hormone (10(-8) M, 48 h) had no effect on the steroidogenesis. However, it increased progesterone secretion (P < 0.05) by about twofold and oestradiol production (P < 0.05) by about 1.6-fold in response to insulin-like growth factor-I (IGF-I) (10(-8) M). Furthermore, it improved IGF-I-induced IGF-I receptor-beta subunit tyrosine phosphorylation and ERK1/2 phosphorylation. In basal state, human adiponectin recombinant also increased rapidly but transiently the ERK1/2, p38 and Akt phosphorylations, whereas it increased more lately the adenosine 5'-monophosphate-activated protein kinase (AMPK) phosphorylation. Thus, AdipoR1 and AdipoR2 are regulated by hCG treatment in rat ovary and adiponectin enhances IGF-I-induced steroidogenesis in granulosa cells.
在哺乳动物中,脂联素及其受体(AdipoR1和AdipoR2)的mRNA在多种组织中表达。然而,脂联素系统在大鼠卵巢中的细胞表达及作用尚未得到研究。在此,我们报告了大鼠卵巢中存在脂联素、AdipoR1和AdipoR2,并研究了其在颗粒细胞中的作用。通过逆转录聚合酶链反应(RT-PCR)和蛋白质印迹法,我们发现卵巢中存在脂联素、AdipoR1和AdipoR2的mRNA及蛋白质。免疫组织化学显示脂联素、AdipoR1和AdipoR2定位于卵泡膜间质(T-I)细胞、黄体、卵母细胞,在颗粒细胞中表达较少。在KGN人颗粒细胞系中,未检测到脂联素的mRNA和蛋白质;AdipoR2表达较弱,而AdipoR1明显存在。对未成熟大鼠先注射孕马血清促性腺激素(PMSG,24小时),然后注射人绒毛膜促性腺激素(hCG,48小时),可使卵巢中脂联素(蛋白质)水平升高约3倍(P<0.05),AdipoR1的mRNA水平升高3倍(P<0.05),蛋白质水平升高1.5倍(P<0.05),而AdipoR2的mRNA和蛋白质水平未发生变化。有趣的是,PMSG处理(24小时)后注射hCG(48小时)可降低血浆脂联素水平,升高血浆胰岛素水平。在原代大鼠颗粒细胞体外实验中,无论有无促卵泡激素(10-8M,48小时),人重组脂联素(5μg/ml)对类固醇生成均无影响。然而,在胰岛素样生长因子-I(IGF-I,10-8M)作用下,它可使孕酮分泌增加约2倍(P<0.05),雌二醇生成增加约1.6倍(P<0.05)。此外,它还可增强IGF-I诱导的IGF-I受体β亚基酪氨酸磷酸化和ERK1/2磷酸化。在基础状态下,人重组脂联素也可迅速但短暂地增加ERK1/2、p38和Akt的磷酸化,而较晚增加腺苷5'-单磷酸激活蛋白激酶(AMPK)的磷酸化。因此,在大鼠卵巢中,AdipoR1和AdipoR2受hCG处理的调控,脂联素可增强颗粒细胞中IGF-I诱导的类固醇生成。