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T淋巴细胞与巨噬细胞的特异性结合IV. 对阳离子、温度和细胞松弛素B敏感机制的依赖性

Specific binding of T lymphocytes to macrophages IV. Dependence on cations, temperature and cytochalasin B-sensitive mechanisms.

作者信息

Lipscomb M F, Ben-Sasson S Z, Tucker T F, Uhr J W

出版信息

Eur J Immunol. 1979 Feb;9(2):119-25. doi: 10.1002/eji.1830090205.

Abstract

Peritoneal exudate lymphocytes (PEL) from immune guinea pigs adhere to macrophages carrying the relevant antigen and are thereby stimulated to proliferate in culture. The resultant PEL represent a population highly enriched with regard to their capacity to specifically rebind to antigen-pulsed macrophages. We have studied the mechanisms underlying specific binding of lymphocytes to macrophages by examining the effects of physical and chemical modifications of the two cell types. Specific binding was inhibited by fixation of cells, metabolic inhibitors, low temperatures, cytochalasin B and divalent cation depletion. After specific binding has taken place, cation depletion, but not cytochalasin B or low temperatures, disrupts binding. These observations indicate that specific binding occurs by a series of discrete events that can be operationally distinguished.

摘要

来自免疫豚鼠的腹腔渗出淋巴细胞(PEL)会黏附于携带相关抗原的巨噬细胞,从而在培养中受到刺激而增殖。由此产生的PEL在特异性重结合抗原脉冲巨噬细胞的能力方面高度富集。我们通过研究两种细胞类型的物理和化学修饰的影响,来探究淋巴细胞与巨噬细胞特异性结合的潜在机制。细胞固定、代谢抑制剂、低温、细胞松弛素B和二价阳离子耗竭均可抑制特异性结合。特异性结合发生后,阳离子耗竭而非细胞松弛素B或低温会破坏结合。这些观察结果表明,特异性结合是通过一系列可在操作上区分的离散事件发生的。

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