Kniep E M, Strelow I, Lohmann-Matthes M L
Abteilung für Immunobiologie, Fraunhofer Institut für Toxikologie, Hannover, Germany.
Immunology. 1992 Feb;75(2):299-304.
Stimulation with lipopolysaccharide (LPS) initiated monocytes to produce interleukin-2 receptor light chain (p55 IL-2R). After stimulation with LPS for 48 hr, considerable quantities of soluble IL-2R were found in the supernatants of monocytes, exceeding even the amount of soluble IL-2R produced by activated T lymphocytes. Cell-associated p55 IL-2R was also increased during the first 24 hr of stimulation, after which time it remained constant. Fractionation of cells and analysis of cytoplasm, mitochondria, plasma membranes and nuclei for the presence of p55 IL-2R revealed that the main portion of receptor was present in the cytoplasm. This led to the conclusion that in monocytes cell-associated p55 IL-2R is not necessarily attached to membranes but is present in a soluble form in the cytoplasm, presumably freshly produced with the aim of being secreted. Stimulation of monocytes with pure recombinant interferon-gamma did not lead to augmentation of p55 IL-2R, as shown by enzyme-linked immunosorbent assay, binding of antibodies directed against the receptor (anti-Tac, CD25) and analysis of p55 IL-2R gene expression.
用脂多糖(LPS)刺激可促使单核细胞产生白细胞介素-2受体轻链(p55 IL-2R)。在用LPS刺激48小时后,在单核细胞的上清液中发现了大量可溶性IL-2R,其数量甚至超过了活化T淋巴细胞产生的可溶性IL-2R的量。在刺激的最初24小时内,细胞相关的p55 IL-2R也有所增加,此后其保持恒定。对细胞进行分级分离,并分析细胞质、线粒体、质膜和细胞核中p55 IL-2R的存在情况,结果显示受体的主要部分存在于细胞质中。由此得出结论,在单核细胞中,细胞相关的p55 IL-2R不一定附着于膜上,而是以可溶性形式存在于细胞质中,推测是为了分泌而新产生的。如酶联免疫吸附测定、针对该受体的抗体结合(抗Tac,CD25)以及p55 IL-2R基因表达分析所示,用纯重组干扰素-γ刺激单核细胞不会导致p55 IL-2R增加。