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淋巴细胞培养基细胞毒性组分不同效应之间的区分。

Differentiation between various effects of cytotoxic fractions of lymphocyte culture medium.

作者信息

Wenzel B, Averdunk R

出版信息

Z Immunitatsforsch Immunobiol. 1977 Dec;153(5):380-94.

PMID:602343
Abstract

This paper describes the partial characterization of supernatants derived from mitogen stimulated lymphocytes by ammonium sulfate precipitation, ultrafiltration on Hollow-Fiber beakers and gelchromatography. Fractions from these purification procedures were tested on FL-target cells and the following target cell alterations were measured: RNA- and protein synthesis, 3H-TdR incorporation, cell number and lysis of target cells. Target cell alterations of control fractions from supernatants of non-stimulated lymphocytes, from culture medium and from FCS were compared to the effects of fractions from activated lymphocytes. 3H-TdR incorporation was not only inhibited by the fractions of activated lymphocyte cultures but also by fractions of various controls. Inhibition of 3H-TdR incorporation disappeared when control fractions were serially diluted. Only fractions of supernatant from activated lymphocytes could lyse target cells. It were the same fractions which still inhibited 3H-TdR incorporation of target cells after serial dilution and which showed stimulating effects on RNA synthesis. MW of fractions which were differentiated from control fractions with respect to target cell lysis were: 90,000, 45,000 and lower than 20,000 d.

摘要

本文描述了通过硫酸铵沉淀、中空纤维烧杯超滤和凝胶色谱法对丝裂原刺激淋巴细胞产生的上清液进行部分表征的过程。对这些纯化程序得到的组分在FL靶细胞上进行测试,并测量了以下靶细胞变化:RNA和蛋白质合成、3H-TdR掺入、细胞数量以及靶细胞裂解。将未刺激淋巴细胞上清液、培养基和胎牛血清的对照组分对靶细胞的影响与活化淋巴细胞组分的作用进行了比较。3H-TdR掺入不仅受到活化淋巴细胞培养物组分的抑制,也受到各种对照组分的抑制。当对照组分进行系列稀释时,3H-TdR掺入的抑制作用消失。只有活化淋巴细胞上清液的组分能够裂解靶细胞。在系列稀释后仍能抑制靶细胞3H-TdR掺入并对RNA合成有刺激作用的是相同的组分。与对照组分在靶细胞裂解方面有差异的组分的分子量为:90,000、45,000和低于20,000 d。

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