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肿瘤坏死因子-α和白细胞介素-6调节人单核细胞中脑源性神经营养因子的分泌。

Tumor necrosis factor-alpha and interleukin-6 regulate secretion of brain-derived neurotrophic factor in human monocytes.

作者信息

Schulte-Herbrüggen Olaf, Nassenstein Christina, Lommatzsch Marek, Quarcoo David, Renz Harald, Braun Armin

机构信息

Department of Neurology, Charité, Humboldt University, Berlin, Germany.

出版信息

J Neuroimmunol. 2005 Mar;160(1-2):204-9. doi: 10.1016/j.jneuroim.2004.10.026. Epub 2004 Dec 22.

Abstract

Activated macrophages have been shown to produce brain-derived neurotrophic factor (BDNF) in diseases such as multiple sclerosis (MS) or allergic bronchial asthma (BA). However, there is little data on BDNF regulation in these cells. We demonstrate that unstimulated human peripheral blood monocytes, but not lymphocytes, constitutively secrete BDNF. IL-6 and TNF-alpha specifically enhanced BDNF secretion in monocytes, whereas typical Th1- and Th2-cytokines did not show any effect. None of the cytokines induced BDNF secretion in T- or B-cells. Thus, our data provide evidence that IL-6 and TNF-alpha represent a specific link between monocyte infiltration and neuronal changes in inflammatory diseases.

摘要

在诸如多发性硬化症(MS)或过敏性支气管哮喘(BA)等疾病中,已证明活化的巨噬细胞可产生脑源性神经营养因子(BDNF)。然而,关于这些细胞中BDNF调节的资料很少。我们证明,未受刺激的人外周血单核细胞而非淋巴细胞可组成性分泌BDNF。白细胞介素-6(IL-6)和肿瘤坏死因子-α(TNF-α)可特异性增强单核细胞中BDNF的分泌,而典型的Th1和Th2细胞因子则无任何作用。没有一种细胞因子能诱导T细胞或B细胞分泌BDNF。因此,我们的数据表明,IL-6和TNF-α代表了炎症性疾病中单核细胞浸润与神经元变化之间的特定联系。

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