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成纤维细胞生长因子4诱导猪滋养外胚层细胞迁移是通过AKT细胞信号通路介导的。

Fibroblast growth factor 4-induced migration of porcine trophectoderm cells is mediated via the AKT cell signaling pathway.

作者信息

Jeong Wooyoung, Lee Jieun, Bazer Fuller W, Song Gwonhwa, Kim Jinyoung

机构信息

Department of Animal Resources Science, Dankook University, Cheonan, Republic of Korea.

Center for Animal Biotechnology and Genomics and Department of Animal Science, Texas A&M University, College Station, TX, USA.

出版信息

Mol Cell Endocrinol. 2016 Jan 5;419:208-16. doi: 10.1016/j.mce.2015.10.020. Epub 2015 Oct 28.

Abstract

During early pregnancy, a well-coordinated communication network between the conceptus and maternal uterus is especially crucial in pigs in which there is a protracted pre-attachment phase prior to implantation. This network is regulated by an astonishing number of molecules such as growth factors. Fibroblast growth factor 4 (FGF4) is a multipotent growth factor that elicits diverse biological actions on various types of cells and tissues. In pigs, FGF4 and its receptors are expressed in the uterine endometrium and conceptus during early pregnancy, but less is known about the FGF4-mediated regulation of conceptus growth during peri-implantation period of pregnancy. Therefore, the aims of the present study were to investigate: 1) expression of endometrial FGF4 mRNA during early pregnancy; 2) up-regulation of FGF receptor expression in porcine trophectoderm (pTr) cells in response to FGF4; and 3) FGF-induced intracellular signaling and cellular activities in pTr cells. In vitro cultured pTr cells incubated with different concentrations of recombinant FGF4 (0-50 ng/ml) responded with a dose-dependent increase in AKT phosphorylation of 2.9-fold at 20 ng/ml FGF4. Within 30 min after treatment with 20 ng/ml FGF4, the abundances of p-AKT, p-P90RSK and p-RPS6 proteins increased 2.1-, 5.2- and 3.2-fold, respectively, and then returned to basal levels by 120 min. To ensure that the stimulatory effect of FGF4 on AKT signaling was p-AKT-dependent, pTr cells were pre-incubated with an AKT inhibitor (LY294002) for 1 h prior to FGF4 treatment. 20 μM of LY294002 decreased FGF4-induced p-AKT, p-P90RSK and p-RPS6 proteins. Immunofluorescence analyses revealed that p-RPS6 proteins were abundant within the cytoplasm of FGF4-treated cells, but present at basal levels in the presence of LY294002. Furthermore, FGF4 increased migration of pTr cells and LY294002 significantly reduced this effect. Results of the present study suggest that activation of the FGF receptor(s) on trophectoderm cells by FGF4 secreted by conceptus/endometrium transduces its signal through the phosphatidylinositol 3-kinase (PI3K)/AKT pathway which is linked to migration of trophectoderm cells that is critical to development of the porcine conceptus.

摘要

在妊娠早期,对于猪而言,在着床前存在一个漫长的未着床期,此时胚胎与母体子宫之间协调良好的通讯网络尤为关键。这个网络受众多分子如生长因子的调控。成纤维细胞生长因子4(FGF4)是一种多能生长因子,对各种类型的细胞和组织会引发多种生物学作用。在猪中,妊娠早期FGF4及其受体在子宫内膜和胚胎中表达,但关于妊娠着床期FGF4介导的胚胎生长调控知之甚少。因此,本研究的目的是探究:1)妊娠早期子宫内膜FGF4 mRNA的表达;2)猪滋养外胚层(pTr)细胞中FGF受体表达对FGF4的上调反应;3)FGF诱导的pTr细胞内信号传导和细胞活性。用不同浓度的重组FGF4(0 - 50 ng/ml)体外培养pTr细胞,在20 ng/ml FGF4时,AKT磷酸化呈剂量依赖性增加2.9倍。用20 ng/ml FGF4处理后30分钟内,p - AKT、p - P90RSK和p - RPS6蛋白丰度分别增加2.1倍、5.2倍和3.2倍,然后在120分钟时恢复到基础水平。为确保FGF4对AKT信号的刺激作用依赖于p - AKT,在FGF4处理前1小时,用AKT抑制剂(LY294002)预孵育pTr细胞。20 μM的LY294002可降低FGF4诱导的p - AKT、p - P90RSK和p - RPS6蛋白。免疫荧光分析显示,p - RPS6蛋白在FGF4处理的细胞胞质内丰富,但在存在LY294002时处于基础水平。此外,FGF4增加了pTr细胞的迁移,而LY294002显著降低了这种作用。本研究结果表明,胚胎/子宫内膜分泌的FGF4激活滋养外胚层细胞上的FGF受体,通过磷脂酰肌醇3 -激酶(PI3K)/AKT途径转导其信号,该途径与滋养外胚层细胞迁移相关,而滋养外胚层细胞迁移对猪胚胎发育至关重要。

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