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单核因子对人星形胶质细胞产生粒细胞集落刺激因子和粒细胞巨噬细胞集落刺激因子的调节作用。I. 白细胞介素-1α和白细胞介素-1β的作用

Monokine modulation of human astroglial cell production of granulocyte colony-stimulating factor and granulocyte-macrophage colony-stimulating factor. I. Effects of IL-1 alpha and IL-beta.

作者信息

Tweardy D J, Mott P L, Glazer E W

机构信息

Department of Medicine, University of Pittsburgh School of Medicine, PA.

出版信息

J Immunol. 1990 Mar 15;144(6):2233-41.

PMID:1690240
Abstract

Granulocyte (G)-CSF and granulocyte-macrophage (GM)-CSF enhance phagocyte survival and function and are produced by fibroblasts and endothelial cells after induction by inflammatory mediators such as IL-1. Our ability to detect G-CSF and GM-CSF activity in the conditioned medium of the human astroglial tumor cell line, U87MG, and molecularly clone the cDNA for G-CSF from a U87MG cDNA library raised the possibility that astroglial cells are capable of G-CSF and GM-CSF production within the central nervous system; if so, the production of these CSF by astroglial cells may be inducible by IL-1. We examined the effects of IL-1 alpha and IL-1 beta on the production of G-CSF and GM-CSF by U87MG and U373MG, another astroglial tumor cell line that does not constitutively produce CSF. We demonstrate that both U87MG and U373MG can be induced to produce G-CSF and GM-CSF by exposure to IL-1 alpha and IL-1 beta. This response, measured by accumulation of increased CSF mRNA, is rapid, sensitive and due to the enhanced stability of CSF message following IL-1 exposure. The implications of these findings to the immunopathogenesis of central nervous system infections are discussed.

摘要

粒细胞集落刺激因子(G-CSF)和粒细胞巨噬细胞集落刺激因子(GM-CSF)可提高吞噬细胞的存活率和功能,在诸如白细胞介素-1等炎症介质诱导后,由成纤维细胞和内皮细胞产生。我们能够在人星形胶质细胞瘤细胞系U87MG的条件培养基中检测到G-CSF和GM-CSF活性,并从U87MG cDNA文库中分子克隆G-CSF的cDNA,这增加了星形胶质细胞能够在中枢神经系统内产生G-CSF和GM-CSF的可能性;如果是这样,星形胶质细胞产生这些集落刺激因子可能受白细胞介素-1诱导。我们研究了白细胞介素-1α和白细胞介素-1β对U87MG和U373MG(另一种非组成性产生集落刺激因子的星形胶质细胞瘤细胞系)产生G-CSF和GM-CSF的影响。我们证明,通过暴露于白细胞介素-1α和白细胞介素-1β,U87MG和U373MG均可被诱导产生G-CSF和GM-CSF。通过增加的集落刺激因子mRNA积累来衡量,这种反应迅速、敏感,且是由于白细胞介素-1暴露后集落刺激因子信息的稳定性增强所致。本文讨论了这些发现对中枢神经系统感染免疫发病机制的意义。

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