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系统性红斑狼疮患者B细胞产生B细胞刺激因子的情况。

Production of B cell-stimulating factors by B cells in patients with systemic lupus erythematosus.

作者信息

Tanaka Y, Saito K, Shirakawa F, Ota T, Suzuki H, Eto S, Yamashita U

机构信息

First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan.

出版信息

J Immunol. 1988 Nov 1;141(9):3043-9.

PMID:3262675
Abstract

The production of B cell-stimulating factors (BSF) by B cells in patients with systemic lupus erythematosus (SLE) was studied in vitro. B cells from SLE patients markedly proliferated and differentiated into Ig-producing cells by in vitro culture without any stimulation. The culture supernatant of these B cells contained BSF activity that stimulated Staphylococcus aureus Cowan I-treated normal B cells to proliferate and differentiate into Ig-producing cells. By a Percoll gradient density centrifugation, BSF-producing cells were enriched in the higher density fraction, but were reduced in the lower density fraction. The BSF also stimulated the proliferation and the differentiation of SLE B cells. By a Percoll gradient density centrifugation, SLE B cells responsive to the BSF were enriched in the higher density fraction, but were reduced in the lower density fraction. The Mr of the BSF was estimated as about 18,000 Da by Sephacryl S-200 column chromatography. The BSF fraction did not possess IL-2 and IFN activity, but possessed IL-1 activity, which stimulated murine thymocyte proliferative responses. The BSF activity was partially, but not completely, absorbed by an anti-IL-1 alpha antibody. Furthermore, the BSF possessed IL-4 activity, which induced not only the proliferative responses of normal B cells stimulated with B cell mitogens, but also the expression of low affinity Fc epsilon R/CD23 on normal B cells. The BSF also possessed IL-6 activity, which induced the proliferative responses of IL-6-dependent hybridoma cells, MH-60 BSF2. Moreover, human rIL-1, rIL-4, and rIL-6 stimulated SLE B cells. These results suggest that SLE B cells spontaneously produce the BSF such as IL-1 alpha, IL-4, and IL-6 and express their receptors on their surface, and the interaction between the BSF and their receptors stimulates SLE B cells to spontaneously proliferate and differentiate into Ig-producing cells as an autocrine mechanism.

摘要

对系统性红斑狼疮(SLE)患者B细胞产生B细胞刺激因子(BSF)进行了体外研究。SLE患者的B细胞在无任何刺激的体外培养中显著增殖并分化为产生Ig的细胞。这些B细胞的培养上清液含有BSF活性,可刺激经金黄色葡萄球菌考恩I处理的正常B细胞增殖并分化为产生Ig的细胞。通过Percoll梯度密度离心,产生BSF的细胞在较高密度组分中富集,而在较低密度组分中减少。该BSF也刺激SLE B细胞的增殖和分化。通过Percoll梯度密度离心,对BSF有反应的SLE B细胞在较高密度组分中富集,而在较低密度组分中减少。通过Sephacryl S - 200柱层析估计BSF的Mr约为18,000 Da。BSF组分不具有IL - 2和IFN活性,但具有IL - 1活性,可刺激小鼠胸腺细胞增殖反应。BSF活性被抗IL - 1α抗体部分但不完全吸收。此外,该BSF具有IL - 4活性,不仅可诱导被B细胞有丝分裂原刺激的正常B细胞的增殖反应,还可诱导正常B细胞上低亲和力FcεR/CD23的表达。该BSF还具有IL - 6活性,可诱导IL - 6依赖性杂交瘤细胞MH - 60 BSF2的增殖反应。此外,人重组IL - 1、重组IL - 4和重组IL - 6刺激SLE B细胞。这些结果表明,SLE B细胞自发产生诸如IL - 1α、IL - 4和IL - 6等BSF,并在其表面表达它们的受体,并且BSF与其受体之间的相互作用作为一种自分泌机制刺激SLE B细胞自发增殖并分化为产生Ig的细胞。

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