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活化淋巴细胞可溶性因子的生物化学与体外活性

The biochemistry and in vitro activity of soluble factors of activated lymphocytes.

作者信息

Sorg C

出版信息

Mol Cell Biochem. 1979 Dec 14;28(1-3):149-67. doi: 10.1007/BF00223364.

Abstract

Activated lymphocytes release numerous products which are either synthesized de novo or in increased amounts; some of these products play a role in the regulation of the immune response and are designated as mediators of cellular immune reactions or lymphokines. The first lymphokine described was the macrophage migration inhibitory factor (MIF) which has been studied most extensively with regard to its chemical and biological properties. Using sensitive radiolabelling techniques and an antiserum against highly purified fractions of MIF we were able to identify several products of activated guinea pig lymphocytes with different molecular weights of 15.000, 30.000, 45.000, 60.000 which all had an isoelectric point of 5.2 and were all inhibitory to macrophage migration. It is suggested, that these molecules are oligomers of a common subunit of molecular weight 15.000. It was further shown, that molecules of the same physical-chemical and serological characteristics are produced by activated B-cells, L2C leukemia cells and growing fibroblasts, thus further substantiating earlier reports on the production of MIF by lymphoid and non-lymphoid cells. The described molecules were also shown not to contain determinants of the major histocompatibility complex and to be distinct from lymphotoxin, another lymphocyte activation product. It is concluded, that MIF is not a single molecule but rather a system of structurally related molecules. Their interaction with macrophages and possible relationships to macrophage activating factor is discussed.

摘要

活化的淋巴细胞会释放大量产物,这些产物要么是重新合成的,要么是产量增加的;其中一些产物在免疫反应调节中发挥作用,被称为细胞免疫反应介质或淋巴因子。最早被描述的淋巴因子是巨噬细胞移动抑制因子(MIF),就其化学和生物学特性而言,它得到了最广泛的研究。利用灵敏的放射性标记技术和针对高度纯化的MIF组分的抗血清,我们能够鉴定出活化的豚鼠淋巴细胞产生的几种分子量不同的产物,分别为15,000、30,000、45,000、60,000,它们的等电点均为5.2,且都能抑制巨噬细胞移动。有人提出,这些分子是分子量为15,000的共同亚基的寡聚体。进一步的研究表明,具有相同物理化学和血清学特征的分子也由活化的B细胞、L2C白血病细胞和正在生长的成纤维细胞产生,从而进一步证实了早期关于淋巴细胞和非淋巴细胞产生MIF的报道。所描述的分子还被证明不包含主要组织相容性复合体的决定簇,并且与另一种淋巴细胞活化产物淋巴毒素不同。得出的结论是,MIF不是单一分子,而是一个结构相关分子的系统。文中讨论了它们与巨噬细胞的相互作用以及与巨噬细胞活化因子可能的关系。

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