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细胞培养和亨廷顿病转基因小鼠模型以及亨廷顿病患者纹状体组织中,细胞因子和内源性大麻素系统受 NF-κB p65/RelA 共同调控。

The cytokine and endocannabinoid systems are co-regulated by NF-κB p65/RelA in cell culture and transgenic mouse models of Huntington's disease and in striatal tissue from Huntington's disease patients.

机构信息

Department of Pharmacology, Dalhousie University, 6th Fl. Sir Charles Tupper Medical Bldg, 5850 College St, Halifax, NS B3H 4R2, Canada.

Department of Pathology, Dalhousie University, 11th Fl. Sir Charles Tupper Medical Bldg, 5850 College St, Halifax, NS B3H 4R2, Canada.

出版信息

J Neuroimmunol. 2014 Feb 15;267(1-2):61-72. doi: 10.1016/j.jneuroim.2013.12.008. Epub 2013 Dec 12.

Abstract

Transcriptional dysregulation is a major pathological feature of Huntington's disease (HD). The goal of this study was to understand how p65/RelA co-regulated genes, specifically those of the cytokine and endocannabinoid systems, were affected in HD. p65/RelA levels were lower in human HD tissue and R6/2 HD mice, as were the levels of the type 1 cannabinoid receptor (CB1), IL-1β, IL-8, CCL5, GM-CSF, MIP-1β, and TNFα, all of which may be regulated by p65/RelA. Activation of p65/RelA restored CB1 and CCL5 expression in STHdh cell models of HD. Therefore, p65/RelA activation may normalize the expression of some genes in HD.

摘要

转录失调是亨廷顿病 (HD) 的主要病理特征。本研究的目的是了解 p65/RelA 共同调控的基因,特别是细胞因子和内源性大麻素系统的基因,在 HD 中是如何受到影响的。在人类 HD 组织和 R6/2 HD 小鼠中,p65/RelA 水平较低,1 型大麻素受体 (CB1)、IL-1β、IL-8、CCL5、GM-CSF、MIP-1β 和 TNFα 的水平也较低,这些都可能受 p65/RelA 调控。p65/RelA 的激活恢复了 STHdh 细胞模型中 HD 中 CB1 和 CCL5 的表达。因此,p65/RelA 的激活可能使 HD 中一些基因的表达正常化。

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