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星形胶质细胞条件培养基和生长因子调节原代培养星形胶质细胞的增殖和分化。

Astroglial-conditioned media and growth factors modulate proliferation and differentiation of astrocytes in primary culture.

作者信息

Bramanti Vincenzo, Campisi Agata, Tomassoni Daniele, Costa Antonino, Fisichella Alfredo, Mazzone Venera, Denaro Luca, Avitabile Marcello, Amenta Francesco, Avola Roberto

机构信息

Section of Biochemistry and Molecular Biology, Department of Chemical Sciences, University of Catania, Viale Andrea Doria, 6, Catania, Italy.

出版信息

Neurochem Res. 2007 Jan;32(1):49-56. doi: 10.1007/s11064-006-9224-6. Epub 2006 Dec 7.

Abstract

Astroglial conditioned media (ACM) influence the development and maturation of cultured nerve cells and modulate neuron-glia interaction. To clarify mechanisms of astroglial cell proliferation/differentiation in culture, incorporation of [methyl-3H]-thymidine or [5,6-3H]-uridine in cultured astrocytes was assessed. Cultures were pre-treated with epidermal growth factor (EGF), insulin (INS), insulin-like growth factor-I (IGF-I), and basic fibroblast growth factor (bFGF) and subsequently with ACM. DNA labeling revealed a marked stimulatory effect of ACM from 15 days in vitro (DIV) cultures in 30 DIV astrocytes after 12 h pre-treatment with growth factors. The main effects were found after INS or EGF pre-treatment in 30 DIV cultures. ACM collected from 15 or 60 or 90 DIV increased RNA labeling of 15 and 30 DIV astrocyte cultures, being the highest value that of 30 DIV cultures added with ACM from 90 DIV. The findings of increased DNA labeling after EGF or INS pre-treatment in 30 DIV cultures, followed by addition of ACM from 15 DIV cultures, suggest that these phenomena may depend by extra cellular signal-regulated kinase 1 (ERK1) activation.

摘要

星形胶质细胞条件培养基(ACM)影响培养的神经细胞的发育和成熟,并调节神经元与胶质细胞的相互作用。为了阐明培养中星形胶质细胞增殖/分化的机制,评估了[甲基 - 3H] - 胸腺嘧啶核苷或[5,6 - 3H] - 尿苷掺入培养的星形胶质细胞中的情况。培养物先用表皮生长因子(EGF)、胰岛素(INS)、胰岛素样生长因子 - I(IGF - I)和碱性成纤维细胞生长因子(bFGF)预处理,随后用ACM处理。DNA标记显示,在用生长因子预处理12小时后,来自体外15天(DIV)培养物的ACM对30 DIV星形胶质细胞有显著的刺激作用。主要作用在30 DIV培养物经INS或EGF预处理后发现。从15或60或90 DIV收集的ACM增加了15和30 DIV星形胶质细胞培养物的RNA标记,其中最高值是添加了来自90 DIV的ACM的30 DIV培养物的值。在30 DIV培养物中经EGF或INS预处理后,再添加来自15 DIV培养物的ACM后DNA标记增加的结果表明,这些现象可能依赖于细胞外信号调节激酶1(ERK1)的激活。

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