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促胃液素(ghrelin)通过 ERK1/2 和 PI-3K 信号通路调控猪卵巢颗粒细胞增殖和凋亡

ERK 1/2 and PI-3 kinase pathways as a potential mechanism of ghrelin action on cell proliferation and apoptosis in the porcine ovarian follicular cells.

机构信息

Department of Physiology and Toxicology of Reproduction, Animal Physiology, Institute of Zoology, Jagiellonian University, Cracow, Poland.

出版信息

J Physiol Pharmacol. 2010 Aug;61(4):451-8.

PMID:20814073
Abstract

Recently, we reported the stimulatory effect of ghrelin on ovarian cell proliferation in parallel with the inhibitory action of ghrelin on cell apoptosis. The aim of the presented data propose local activation of extracellular signal-regulated protein kinase 1 and 2 (ERK 1/2) and phosphoinositide-3 (PI-3) kinase pathways as a mechanism of ghrelin effect in the porcine ovary. To test this hypothesis, action of ghrelin on levels of ERK 1/2 with PI-3 kinase activity and protein expression using ELISA and western blot analysis, respectively, was examined. Additionally, to determine which pathways (ERK 1/2 or PI-3 kinase) are the potential signals of ghrelin-mediated cell proliferation and apoptosis in ovarian cells, we used PD098059 (50 microM) and wortmannin (200 microM), well-known inhibitors of these kinases. Treatment of ovarian coculture cells with ghrelin (100, 250, 500 and 1000 pg/ml) showed stimulation of phospho-ERK 1/2 levels and PI-3 kinase activity, with the maximum effect observed after 15 min of cell incubation. Additionally, western blot analysis indicated that ghrelin increased expression of both kinases. Moreover, ghrelin used in combination with PD098059 or wortmannin significantly decreased cell proliferation, which was measured by the Alamar Blue assay and increased apoptosis, which was measured by caspase - 3 activity and DNA fragmentation. In conclusion, these results suggest that the ERK 1/2 and PI-3 kinase pathways may be potential signals of ghrelin mediate the cell proliferation and apoptosis of ovary cells.

摘要

最近,我们报道了生长激素释放肽对卵巢细胞增殖的刺激作用,同时生长激素释放肽对细胞凋亡具有抑制作用。本研究数据旨在提出细胞外信号调节蛋白激酶 1 和 2(ERK 1/2)和磷酸肌醇-3(PI-3)激酶通路的局部激活作为生长激素在猪卵巢中作用的机制。为了验证这一假设,我们使用 ELISA 和 Western blot 分析分别检测了生长激素对 ERK 1/2 水平、PI-3 激酶活性和蛋白表达的影响。此外,为了确定哪些途径(ERK 1/2 或 PI-3 激酶)是生长激素介导的卵巢细胞增殖和凋亡的潜在信号,我们使用了 PD098059(50μM)和wortmannin(200μM),这两种激酶的已知抑制剂。用生长激素(100、250、500 和 1000pg/ml)处理卵巢共培养细胞显示出磷酸化 ERK 1/2 水平和 PI-3 激酶活性的刺激作用,在细胞孵育 15 分钟后观察到最大效应。此外,Western blot 分析表明生长激素增加了两种激酶的表达。此外,生长激素与 PD098059 或 wortmannin 联合使用可显著降低细胞增殖,这可通过 Alamar Blue 测定法测量,并且增加细胞凋亡,这可通过 caspase-3 活性和 DNA 片段化来测量。总之,这些结果表明 ERK 1/2 和 PI-3 激酶途径可能是生长激素介导卵巢细胞增殖和凋亡的潜在信号。

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