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[细胞因子或脂多糖激活的培养人单核细胞诱导纤连蛋白生成]

[Cultured human monocytes activated by cytokines or lipopolysaccharide induce fibronectin].

作者信息

Kitamura N, Nishinarita S, Takizawa T, Tomita Y, Hayama T, Horie T

机构信息

First Department of Internal Medicine, Nihon University School of Medicine.

出版信息

Nihon Rinsho Meneki Gakkai Kaishi. 1995 Apr;18(2):178-87. doi: 10.2177/jsci.18.178.

Abstract

We studied the effects of cytokines such as IL-1 alpha, IL-6 and TNF alpha, and lipopolysaccharide (LPS) on cultured human monocytes. Increased fibronectin (FN) production, as a indicator of the activation of monocytes, was observed with any cytokines or LPS stimulation those were added in the culture medium. These increased FN production by cytokines showed a dose dependent fashion, and 4 hours culture with these cytokines was enough to obtain the amount of FN measured with radioimmunoassay. The combination of sub-optimal dose of cytokines (IL-1 alpha + IL-6, IL-1 alpha, IL-6 + TNF alpha), that could not induce substantial amount of FN with any single cytokine, also could induce FN by cultured monocytes. The specificity of cytokines for the FN production by cultured monocytes was confirmed by the neutralization using monoclonal antibodies specific for each monokines. Northern blot analysis with cDNA specific for FN confirmed the expression of FN mRNA in cultured monocytes stimulated with cytokines or LPS. Cytokine network plays an essential role for immune and inflammatory reaction, and FN has been shown to induce monokines through VLA-5 receptor on cultured monocytes. Our data suggests that monocytes may not always require high concentration of cytokines for the activation of monocytes in vitro, and that the synergistic action of low concentration of cytokines for the activation was enough for the progression of immune or inflammatory reaction.

摘要

我们研究了白细胞介素 -1α、白细胞介素 -6 和肿瘤坏死因子α等细胞因子以及脂多糖(LPS)对培养的人单核细胞的影响。作为单核细胞活化指标的纤连蛋白(FN)产生增加,在向培养基中添加任何细胞因子或 LPS 刺激时均有观察到。这些细胞因子导致的 FN 产生增加呈剂量依赖性,用这些细胞因子培养 4 小时就足以获得用放射免疫测定法测得的 FN 量。次优剂量的细胞因子组合(白细胞介素 -1α + 白细胞介素 -6、白细胞介素 -1α、白细胞介素 -6 + 肿瘤坏死因子α),单独使用任何一种细胞因子都不能诱导产生大量的 FN,但也能诱导培养的单核细胞产生 FN。通过使用针对每种单核因子的单克隆抗体进行中和,证实了细胞因子对培养的单核细胞产生 FN 的特异性。用 FN 特异性 cDNA 进行的 Northern 印迹分析证实了在细胞因子或 LPS 刺激的培养单核细胞中 FN mRNA 的表达。细胞因子网络在免疫和炎症反应中起重要作用,并且已经表明 FN 通过培养单核细胞上的 VLA -5 受体诱导单核因子。我们的数据表明,在体外单核细胞激活可能并不总是需要高浓度的细胞因子,低浓度细胞因子的协同作用足以促进免疫或炎症反应的进展。

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