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聚蔗糖和植物血凝素对人淋巴细胞的协同作用。

Synergistical effects of ficoll and phytohemagglutinin on human lymphocytes.

作者信息

Baron D, Glaesener J J, Schellinger G, Petres J

出版信息

Arch Dermatol Res. 1978 May 31;261(3):273-9. doi: 10.1007/BF00455296.

Abstract

The influence of increasing concentration of the highly polymerized dectran Ficoll on cultured peripheral human blood lymphocytes stimulated or not stimulated by PHA was studied. The incorporation of 14C-thymidine into acid-insoluble material of unstimulated lymphocytes has not been influenced in the presence of increasing concentrations of Ficoll either pretreated with chelating resin or not pretreated. Ficoll not pretreated with chelating resin potentiates the PHA-induced stimulation by the factor 4.3 at 0.1 mg Ficoll/ml culture medium, and by the factor 3.2 at 1.0 mg/ml when PHA stimulated HPBL were used. Ficoll after pretreatment with chelating resin does not influence the DNA-synthesis at 0.1 mg Ficoll/ml medium, but causes a drop of the incorporation of 14C-thymidine by the factor 2.0 at 1.0 mg/ml. Using 10.0 mg per ml, both Ficoll preparation cause a decrease of the DNA-synthesis by the factor 2.5--3.0--probably a cytotoxic effect. The results obtained with emission spectrographic analysis and conductivity measurements show, that Ficoll after treatment with chelating resin contains about 10 times more ions (Mg, Ca, Na, Si) and has a 3.2-fold higher conductivity then Ficoll without pretreatment. It is possible that phenomena like electrochemical changes on the surface of the lymphocytes and osmotic alterations in the culture medium are responsible for these effects.

摘要

研究了高聚合度葡聚糖Ficoll浓度增加对经PHA刺激或未刺激的人外周血淋巴细胞培养的影响。无论是否用螯合树脂预处理,随着Ficoll浓度增加,未刺激淋巴细胞酸不溶性物质中14C-胸腺嘧啶核苷的掺入均未受到影响。当使用PHA刺激的人外周血淋巴细胞时,未用螯合树脂预处理的Ficoll在0.1mg Ficoll/ml培养基中使PHA诱导的刺激增强4.3倍,在1.0mg/ml时增强3.2倍。用螯合树脂预处理后的Ficoll在0.1mg Ficoll/ml培养基中不影响DNA合成,但在1.0mg/ml时使14C-胸腺嘧啶核苷掺入量下降2.0倍。当使用10.0mg/ml时,两种Ficoll制剂均使DNA合成下降2.5 - 3.0倍——可能是细胞毒性作用。发射光谱分析和电导率测量结果表明,用螯合树脂处理后的Ficoll含有的离子(Mg、Ca、Na、Si)约多10倍,电导率比未预处理的Ficoll高3.2倍。淋巴细胞表面的电化学变化和培养基中的渗透改变等现象可能是造成这些效应的原因。

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