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The promoting effect of retinoic acid on proliferation of chicken primordial germ cells by increased expression of cadherin and catenins

机译:视黄酸通过增加钙黏着蛋白和连环蛋白的表达来促进鸡原始生殖细胞的增殖

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摘要

Proliferation and cellular aggregation are both crucial features for survival and self-renewal of primordial germ cells (PGCs). Adhesive proteins play pivotal roles in cell–cell adhesion and signal exchanges under the influence of cytokines, growth factors and bioactive metabolites such as retinoic acid (RA). In this study, proliferation-promoting effect of RA on chicken PGCs was investigated by revealing changes in adhesive proteins E-cadherin and α/β catenins. PGCs were isolated from the genital ridge of 4-day-old chicken embryos and cultured on embryonic fibroblast feeder. RA (10−7–10−5 M) increased PGCs aggregation and mRNA expression of E-cadherin and α/β-catenins. Furthermore, E-cadherin and β-catenin protein expression levels were increased by RA treatment. However, RA-elicited effect was significantly attenuated by a PKC inhibitor H7. In addition, the number and area of PGC colonies were increased by RA treatment at 10−7–10−5 M. Again, this increase was reduced by combined treatment of H7. The proliferating effect of RA on PGCs was further confirmed by increased mRNA expression of cyclins, CCND1 and CCNE1, and cyclin-dependent kinases 6 and 2, which are critical for G1–S progression in cell cycle. Moreover, flow cytometry analysis confirmed that RA-treated PGC populations displayed a significant increase in the proportion of S and G2 phase cells. Likewise, this stimulating action was hindered by combined H7 treatment. These results indicate that RA, as a bioactive metabolite of vitamin A, may promote PGC proliferation and increase intercellular aggregation of PGCs via E-cadherin and α/β-catenins expression through the PKC signaling pathway.
机译:增殖和细胞聚集都是原始生殖细胞(PGC)存活和自我更新的关键特征。粘附蛋白在细胞因子,生长因子和视黄酸(RA)等生物活性代谢物的影响下,在细胞间粘附和信号交换中起关键作用。在这项研究中,通过揭示粘附蛋白E-钙粘蛋白和α/β连环蛋白的变化,研究了RA对鸡PGC的增殖促进作用。从4天大的鸡胚的生殖脊中分离出PGC,并在胚胎成纤维细胞饲养器上培养。 RA(10 −7 –10 −5 M)增加E-钙粘蛋白和α/β-连环蛋白的PGC聚集和mRNA表达。此外,RA处理可增加E-cadherin和β-catenin蛋白的表达水平。然而,PKC抑制剂H 7 显着减弱了RA引起的作用。此外,RA处理在10 −7 –10 −5 M时增加了PGC菌落的数量和面积。再次,通过联合处理H减少了这种增加 7 。细胞周期蛋白,CCND1和CCNE1以及细胞周期蛋白依赖性激酶6和2的mRNA表达增加,进一步证实了RA对PGC的增殖作用,这对细胞周期中G1–S进程至关重要。此外,流式细胞仪分析证实,RA处理的PGC群体显示S和G2期细胞的比例显着增加。同样,H 7 联合治疗也阻碍了这种刺激作用。这些结果表明,RA是维生素A的一种生物活性代谢产物,可通过E-钙粘蛋白和通过PKC信号通路表达α/β-catenins促进PGC增殖并增加PGC的细胞间聚集。

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