He Pei Jian, Fujimoto Yasunori, Yamauchi Nobuhiko, Hattori Masa-Aki
Department of Animal and Marine Bioresource Sciences, Faculty of Agriculture Graduate School, Kyushu University, 6-10-1 Hakozaki, Higashi-ku, Fukuoka 812-8581, Japan.
Mol Cell Biochem. 2006 Oct;290(1-2):177-84. doi: 10.1007/s11010-006-9185-8. Epub 2006 Apr 22.
The present study was performed to establish a real-time monitoring of the cAMP response element binding protein (CREB) signalling using granulosa cells, and to assess the modulation of CREB activity by potential ovarian autocrine/paracrine and oocyte-derived factors. Granulosa cells were isolated from porcine follicles and cultured for 2 days, and then transfected with CRE-containing pGL3. The cells were directly stimulated or cultured with FSH, LH, forskolin, or a permeable cAMP analog, and/or IGF-I, EGF, bFGF, TGF-beta2 or TNF-alpha, or cumulus-oocyte complex (COCs) for the real-time monitoring of CREB signaling. The activation pattern of CREB signaling consisted of three distinct phases, i.e., burst, attenuation and refractory. In contrast to FSH, LH, and forskolin, a cAMP analog induced the prolonged activation, although three distinct phases were observed at its high concentration. Of all the autocrine/paracrine factors, only IGF-I slightly induced CREB activity. On the other hand, TGF-beta2 and TNF-alpha significantly repressed FSH-stimulated transcriptional activation of CREB by 30% (P < 0.05) and 45% (P < 0.05), respectively. Additionally, coculture with COCs caused a significant suppression of transcriptional activation of CREB signaling stimulated by FSH. These results indicate that ovarian autocrine/paracrine factors such as IGF-I, TGF-beta2, TNF-alpha and oocyte-derived factors modulate the CREB signaling. The present study provides a new approach for direct signaling study on transcription factors under the influences of potential factors.
本研究旨在利用颗粒细胞建立环磷酸腺苷反应元件结合蛋白(CREB)信号通路的实时监测体系,并评估潜在的卵巢自分泌/旁分泌因子及卵母细胞衍生因子对CREB活性的调节作用。从猪卵泡中分离出颗粒细胞并培养2天,然后用含CRE的pGL3进行转染。直接用促卵泡激素(FSH)、促黄体生成素(LH)、福斯可林或可渗透的环磷酸腺苷类似物,和/或胰岛素样生长因子-I(IGF-I)、表皮生长因子(EGF)、碱性成纤维细胞生长因子(bFGF)、转化生长因子-β2(TGF-β2)或肿瘤坏死因子-α(TNF-α),或卵丘-卵母细胞复合体(COCs)刺激或培养这些细胞,以实时监测CREB信号通路。CREB信号通路的激活模式包括三个不同阶段,即爆发期、衰减期和不应期。与FSH、LH和福斯可林不同,环磷酸腺苷类似物诱导了持续的激活,尽管在高浓度时也观察到三个不同阶段。在所有自分泌/旁分泌因子中,只有IGF-I轻微诱导了CREB活性。另一方面,TGF-β2和TNF-α分别显著抑制FSH刺激的CREB转录激活30%(P<0.05)和45%(P<0.05)。此外,与COCs共培养导致FSH刺激的CREB信号通路转录激活显著受到抑制。这些结果表明,卵巢自分泌/旁分泌因子如IGF-I、TGF-β2、TNF-α以及卵母细胞衍生因子可调节CREB信号通路。本研究为在潜在因子影响下对转录因子进行直接信号研究提供了一种新方法。