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通过 Toll 样受体 3 刺激诱导肾上腺皮质细胞中 CXCL10 趋化因子的产生。

Induction of CXCL10 chemokine in adrenocortical cells by stimulation through toll-like receptor 3.

机构信息

Section for Endocrinology, Institute of Medicine, University of Bergen, N-5020 Bergen, Norway.

出版信息

Mol Cell Endocrinol. 2013 Jan 5;365(1):75-83. doi: 10.1016/j.mce.2012.09.004. Epub 2012 Sep 16.

Abstract

Addison's disease is a prototypic organ-specific autoimmune disease affecting the adrenal cortex. The CXC chemokine ligand 10 (CXCL10) is expressed early in viral infections, and is produced by primary adrenocortical cells stimulated by certain cytokines. CXCL10 is also elevated in the serum of Addison's disease patients. We therefore investigated if the viral RNA substitute polyinosine-polycytidylic acid (poly (I:C)) could influence the cytokine induced production of CXCL10 by adrenocortical cells. We found that poly (I:C) could induce CXCL10 in NCI-H295R adrenocortical carcinoma cells, either alone or synergistically along with cytokines interferon-γ and tumor necrosis factor-α. This effect was found to be mediated by toll-like receptor 3 and both nuclear factor κB (NFκB) and signal transducer and activator of transcription-1 (STAT1), but not type I interferons, seemed to be involved. We propose that the combination of environmental and endogenous factors presented here, could contribute to the multifactorial pathogenesis of autoimmune Addison's disease.

摘要

艾迪生病是一种典型的器官特异性自身免疫性疾病,影响肾上腺皮质。趋化因子配体 10(CXCL10)在病毒感染早期表达,并由某些细胞因子刺激的原发性肾上腺皮质细胞产生。艾迪生病患者的血清中也升高了 CXCL10。因此,我们研究了病毒 RNA 替代物聚肌苷酸-聚胞苷酸(poly(I:C))是否会影响细胞因子诱导的肾上腺皮质细胞 CXCL10 的产生。我们发现,poly(I:C)可以单独或与细胞因子干扰素-γ和肿瘤坏死因子-α协同诱导 NCI-H295R 肾上腺皮质癌细胞产生 CXCL10。这种作用是通过 Toll 样受体 3 介导的,涉及核因子 κB(NFκB)和信号转导和转录激活因子 1(STAT1),但似乎不涉及 I 型干扰素。我们提出,这里提出的环境和内源性因素的组合可能有助于自身免疫性艾迪生病的多因素发病机制。

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