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一种新型神经节苷脂,去-N-乙酰基-GM3(II3NeuNH2LacCer),作为表皮生长因子受体激酶的强启动子和细胞生长的刺激剂。

A novel ganglioside, de-N-acetyl-GM3 (II3NeuNH2LacCer), acting as a strong promoter for epidermal growth factor receptor kinase and as a stimulator for cell growth.

作者信息

Hanai N, Dohi T, Nores G A, Hakomori S

机构信息

Department of Biochemical Oncology, Fred Hutchinson Cancer Center, Seattle, Washington.

出版信息

J Biol Chem. 1988 May 5;263(13):6296-301.

PMID:2834372
Abstract

A novel ganglioside, de-N-acetyl-GM3 (neuraminyllactosylceramide, II3NeuNH2LacCer), was found in the monosialoganglioside fraction of A431 cells and B16 melanoma cells by high-performance liquid chromatography, thin-layer chromatography, and immunoblotting with its specific monoclonal antibody DH5. This novel type of membrane ganglioside strongly enhanced the kinase activity associated with the epidermal growth factor (EGF) receptor, and it showed 32, 35, and 12% growth stimulation as compared with control cultures of A431, Swiss 3T3, and B16 melanoma cells, respectively. Exogenously added de-N-acetyl-GM3 did not alter the affinity of EGF binding to its receptor. These properties of de-N-acetyl-GM3 are in striking contrast to those of GM3 and its lyso derivative (lyso-GM3) which were previously shown to inhibit EGF receptor kinase activity and to inhibit growth in the same cells. These data indicate that de-N-acetylation at the sialic acid moiety of GM3 ganglioside is an important mechanism for modulation of EGF-dependent cell growth. The mechanism is antagonistic to that of GM3-dependent modulation of receptor function.

摘要

通过高效液相色谱、薄层色谱以及用其特异性单克隆抗体DH5进行免疫印迹分析,在A431细胞和B16黑色素瘤细胞的单唾液酸神经节苷脂组分中发现了一种新型神经节苷脂,即去N-乙酰基-GM3(神经氨酸乳糖基神经酰胺,II3NeuNH2LacCer)。这种新型膜神经节苷脂强烈增强了与表皮生长因子(EGF)受体相关的激酶活性,与A431、瑞士3T3和B16黑色素瘤细胞的对照培养物相比,它分别显示出32%、35%和12%的生长刺激作用。外源添加的去N-乙酰基-GM3并未改变EGF与其受体结合的亲和力。去N-乙酰基-GM3的这些特性与GM3及其溶血衍生物(溶血-GM)的特性形成鲜明对比,先前研究表明GM3及其溶血衍生物可抑制EGF受体激酶活性并抑制相同细胞的生长。这些数据表明,GM3神经节苷脂唾液酸部分的去N-乙酰化是调节EGF依赖性细胞生长中的一个重要机制。该机制与GM3依赖性受体功能调节机制相反。

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