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趋化因子基因表达的细胞类型及刺激特异性调控。

Cell type and stimulus specific regulation of chemokine gene expression.

作者信息

Ohmori Y, Hamilton T A

机构信息

Department of Immunology, Research Institute, Cleveland Clinic Foundation, Ohio 44195.

出版信息

Biochem Biophys Res Commun. 1994 Jan 28;198(2):590-6. doi: 10.1006/bbrc.1994.1086.

Abstract

The pattern of chemoattractant cytokine gene (IP-10, JE, KC) expression has been examined in BALB/c 3T3 fibroblasts and MC3T3-E1 osteoblasts in response to a variety of different inflammatory stimuli, including IFN gamma, TNF alpha, IL-1 alpha, and IL-6. Both cell types expressed JE and IP-10 mRNAs but the response pattern varied in a stimulus- and gene-dependent fashion. KC mRNA was only expressed in BALB/c 3T3 cells stimulated by IL-1 alpha. The time dependence for expression was distinctive for each gene but was comparable despite different forms of stimulation. Nevertheless, the mechanisms involved in the induction of each gene varied with the stimulus and involved both transcriptional and post-transcriptional components. These findings reflect the diversity of chemokine gene expression in vivo and may be important in mechanistic understanding of the diversity of inflammatory response patterns.

摘要

在BALB/c 3T3成纤维细胞和MC3T3-E1成骨细胞中,研究了趋化因子细胞因子基因(IP-10、JE、KC)在多种不同炎症刺激(包括IFNγ、TNFα、IL-1α和IL-6)作用下的表达模式。两种细胞类型均表达JE和IP-10 mRNA,但反应模式因刺激因素和基因而异。KC mRNA仅在受IL-1α刺激的BALB/c 3T3细胞中表达。每个基因表达的时间依赖性各不相同,但尽管刺激形式不同,其时间依赖性具有可比性。然而,每个基因诱导所涉及的机制随刺激因素而变化,涉及转录和转录后成分。这些发现反映了体内趋化因子基因表达的多样性,可能对从机制上理解炎症反应模式的多样性具有重要意义。

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