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肺炎克雷伯菌糖蛋白提取物RU-41740的免疫活性。III. 类脂多糖和与脂多糖无关分子的作用。

Immunological activities of RU-41740, a glycoprotein extract from Klebsiella pneumoniae. III. Role of LPS-like and LPS-non-related molecules.

作者信息

Vacheron F, Périn S, Kodari E, Smets P, Zalisz R, Guenounou M

机构信息

Laboratoire de Microbiologie, UFR de Médicine, Paris-Ouest, Garches, France.

出版信息

Res Immunol. 1989 Feb;140(2):159-72. doi: 10.1016/0923-2494(89)90080-1.

Abstract

RU-41740, a glycoprotein complex extracted from Klebsiella pneumoniae, is an immunomodulating agent which acts on B cells and macrophages. It has been shown that RU-41740 is composed mainly of two macromolecular fractions, F1, having an LPS-related structure, and P1, with a proteoglycan structure. In the present paper, the effects of these molecules on B cells and on IL-1 and tumour necrosis factor (TNF), production by macrophages were compared. Data reveal that both fractions were mitogenic for murine B cells and induced IL-1 and TNF production by macrophages. The LPS-like fraction (F1) was sensitive to polymyxin B and was unable to activate macrophages and spleen cells from LPS non-responder mice. The P1 fraction was mitogenic for B cells and induced the production of IL-1 and TNF activities by macrophages from LPS non-responder C3H/HeJ mice. The cytotoxic activity was due to TNF alpha, since treatment with anti-TNF alpha antiserum abrogated the lytic activity of supernatants from stimulated macrophages. The differences observed between P1 and F1 fractions in terms of sensitivity to polymyxin B and activity towards C3H/HeJ spleen cells and macrophages suggest that the two structurally distinct molecules isolated from RU-41740 could act at different sites on immunocompetent cells.

摘要

RU - 41740是一种从肺炎克雷伯菌中提取的糖蛋白复合物,是一种作用于B细胞和巨噬细胞的免疫调节剂。已表明RU - 41740主要由两个大分子组分组成,即具有脂多糖相关结构的F1和具有蛋白聚糖结构的P1。在本文中,比较了这些分子对B细胞以及对巨噬细胞产生白细胞介素 - 1(IL - 1)和肿瘤坏死因子(TNF)的影响。数据显示,这两个组分对小鼠B细胞均有促有丝分裂作用,并诱导巨噬细胞产生IL - 1和TNF。脂多糖样组分(F1)对多粘菌素B敏感,且不能激活来自脂多糖无反应小鼠的巨噬细胞和脾细胞。P1组分对B细胞有促有丝分裂作用,并诱导来自脂多糖无反应的C3H/HeJ小鼠的巨噬细胞产生IL - 1和TNF活性。细胞毒性活性归因于TNFα,因为用抗TNFα抗血清处理可消除受刺激巨噬细胞上清液的裂解活性。在对多粘菌素B的敏感性以及对C3H/HeJ脾细胞和巨噬细胞的活性方面,P1和F1组分之间观察到的差异表明,从RU - 41740中分离出的这两个结构不同的分子可能在免疫活性细胞的不同位点起作用。

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