Data in support of NF kappa B and JNK pathways involvement in TLR3-mediated HIV-1 transactivation, expression of IL-6 and transcription factors associated with HIV-1 replication

被引:3
作者
Bhargavan, Biju [1 ]
Woollard, Shawna M. [1 ]
Kanmogne, Georgette D. [1 ]
机构
[1] Univ Nebraska Med Ctr, Dept Pharmacol & Expt Neurosci, Omaha, NE 68198 USA
基金
美国国家卫生研究院;
关键词
TLR3; HIV transactivation; transcription factors; IL-6; human macrophages;
D O I
10.1016/j.dib.2015.12.022
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In the present article, using human monocyte-derived macrophages and cell lines containing integrated copies of the HIV-1 promoter, we show the effects of TLR3 ligands on the pro-inflammatory cytokine IL-6. We further show the effects of TLR3 ligands on HIV-1 transactivation and transcription factors involved in HIV-1 replication. This article complements the data reported by the authors, "Toll-Like receptor-3 mediates HIV-1 transactivation via NF kappa B and JNK pathways, and histone acetylation, but prolonged activation suppresses Tat and HIV-1 replication" (Bhargavan et al., 2015) [1], and the interpretation of these data can be found in the research article published by the authors in Cellular Signaling in 2015 (Bhargavan et al., 2015) [1]. (C) 2015 The Authors. Published by Elsevier Inc. This is an open access article under the CC BY license
引用
收藏
页码:345 / 351
页数:7
相关论文
共 4 条
[1]   Toll-like receptor-3 mediates HIV-1 transactivation via NFκB and JNK pathways and histone acetylation, but prolonged activation suppresses Tat and HIV-1 replication [J].
Bhargavan, Biju ;
Woollard, Shawna M. ;
Kanmogne, Georgette D. .
CELLULAR SIGNALLING, 2016, 28 (02) :7-22
[2]   HIV-1 activates proinflammatory and interferon-inducible genes in human brain microvascular endothelial cells: putative mechanisms of blood-brain barrier dysfunction [J].
Chaudhuri, Anathbandhu ;
Duan, Fenghai ;
Morsey, Brenda ;
Persidsky, Yuri ;
Kanmogne, Georgette D. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2008, 28 (04) :697-711
[3]  
Gorantla Santhi, 2005, Methods Mol Biol, V304, P35
[4]  
Schuitemaker Hanneke, 2005, Methods Mol Biol, V304, P17, DOI 10.1385/1-59259-907-9:017