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Expression of Insulin-like Growth Factor Binding Protein-3 and Regulation of the Insulin-like Growth Factor-Ⅰ Axis in Pig Testis

机译:猪睾丸中胰岛素样生长因子结合蛋白3的表达及胰岛素样生长因子Ⅰ轴的调控

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The stem cell niche is a complex unit comprising key components, such as the extracellular matrix and various paracrine factors, which regulate the differentiation of adult stem cells. In our previous study, we established pig spermatogonial stem cells (pSSCs) in culture and identified the expression of insulin-like growth factor binding protein-3 (IGFBP-3) in pSSCs. The present study investigated not only the expression of IGFBP-3, but also its possible role in pSSCs. In this study, IGFBP-3-expressing cells responded positively to protein gene product 9.5 (PGP9.5), which is a marker for pig spermatogonia. IGFBP-3 expression was significantly increased in 60-day-old pig testes. Additionally, the expression levels of insulin-like growth factor I (IGF-I) and its receptor (IGF-IR) were observed in pSSCs and pig Sertoli cells (pSCs). Furthermore, IGF-I treatment enhanced the proliferation of pSCs and pSSCs when they were co-cultured. Blocking the IGF-I pathway using a specific IGF-IR inhibitor dramatically reduced the proliferation of pSCs. In addition, when heparan sulfate was used to sequester IGFBP-3 from IGF-I binding, a significant increase in the proliferation of pSCs was observed. Exogenous IGF-I treatment also increased the expression level of IGFBP-3 in cultured pSSCs. Furthermore, pSSCs grew well in IGF-I-treated pSC conditioned media. In summary, IGF-I and IGF-IR signaling are important for the proliferation of pSCs, and the germ cell-derived IGFBP-3 had an inhibitory effect on the mitotic activity of IGF-I in pSCs.
机译:干细胞小生境是一个复杂的单元,包含调节成体干细胞分化的关键成分,例如细胞外基质和各种旁分泌因子。在我们之前的研究中,我们在培养物中建立了猪精原干细胞(pSSCs),并鉴定了pSSCs中胰岛素样生长因子结合蛋白3(IGFBP-3)的表达。本研究不仅研究了IGFBP-3的表达,还研究了其在pSSCs中的可能作用。在这项研究中,表达IGFBP-3的细胞对蛋白基因产物9.5(PGP9.5)呈阳性反应,而蛋白基因产物9.5是猪精原细胞的标志物。在60天大的猪睾丸中,IGFBP-3表达显着增加。另外,在pSSCs和猪支持细胞(pSCs)中观察到胰岛素样生长因子I(IGF-1)及其受体(IGF-1R)的表达水平。此外,IGF-I处理在共培养时增强了pSC和pSSC的增殖。使用特定的IGF-1R抑制剂阻断IGF-1途径可显着降低pSC的增殖。另外,当使用硫酸乙酰肝素从IGF-1结合中隔离IGFBP-3时,观察到了pSCs增殖的显着增加。外源IGF-I处理也可提高培养的pSSC中IGFBP-3的表达水平。此外,pSSC在经过IGF-I处理的pSC条件培养基中生长良好。总之,IGF-1和IGF-1R信号传导对于pSCs的增殖是重要的,并且生殖细胞衍生的IGFBP-3对IGC-1在pSCs中的有丝分裂活性具有抑制作用。

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