scholarly journals NF-κB Regulation by IκB Kinase-2 in Rheumatoid Arthritis Synoviocytes

2001 ◽  
Vol 166 (4) ◽  
pp. 2705-2711 ◽  
Author(s):  
Karlfried R. Aupperle ◽  
Brydon L. Bennett ◽  
Zuoning Han ◽  
David L. Boyle ◽  
Anthony M. Manning ◽  
...  
2020 ◽  
Vol 79 (Suppl 1) ◽  
pp. 251.1-251
Author(s):  
J. M. Kim ◽  
H. J. Kang ◽  
S. J. Jung ◽  
B. W. Song ◽  
H. J. Jeong ◽  
...  

Background:Long noncoding RNAs (lncRNAs) have recently emerged as important biological regulators and the aberrant expression of lncRNAs has been reported in various diseases including cancer, cardiovascular disease, and diabetes mellitus. However, the role of lncRNAs in the pathogenesis of rheumatoid arthritis (RA) remains unknown.Objectives:Thus, we studied lncRNAs influenced by IL-1, which is one of the key mediators in the pathogenesis of RA, and also investigated whether regulation of NF-κB activation, which is known to be induced by IL-1, could lead to the changes of expression of those lncRNAs.Methods:Fibroblast-like synoviocytes (FLS) were obtained from the knee joints of the patients with RA. The next-generation sequencing (NGS) data were analyzed to identify differentially expressed lncRNAs between unstimulated RA FLS and IL-1-stimulated RA FLS. The expression levels of the top 5 candidates in NGS data were validated by RT-qPCR using extended number of unstimulated RA FLS and IL-1-stimulated RA FLS. IMD-0560, an inhibitor of IκB kinase (IKK) was used for the regulation of NF-κB activation. Activation and inhibition of NF-κB were confirmed by Western blotting. Changed expressions of the lncRNAs were identified by RT-qPCR.Results:NGS analysis revealed up-regulated 30 lncRNAs and down-regulated 15 lncRNAs in IL-1-treated RA FLS compared with unstimulated RA FLS. Top 5 lncRNAs were selected among 30 lncRNAs up-regulated by IL-1 in RA FLS based on fold-change with P-value cutoff. The up-regulated lncRNAs including NR_046035, NR_027783, NR_033422, NR_003133, and NR_049759 were validated by RT-qPCR. IMD-0560 inhibited phosphorylation of IκBα induced by IL-1 in RA FLS. Overexpression of lncRNAs induced by IL-1 was also inhibited by IMD-0560 in RA FLS.Conclusion:Our study revealed that IL-1 increased the expression of NR_046035, NR_027783, NR_033422, NR_003133, and NR_049759 in RA FLS. In addition, the expression of these lncRNAs was regulated by inhibition of NF-κB activation. Thus, our data suggest that the lncRNAs might be involved in the pathogenesis of RA through NF-κB signaling pathway.References:[1]Long noncoding RNAs and human disease. Trends Cell Biol. 2011 Jun;21(6):354-61.[2]A long noncoding RNA mediates both activation and repression of immune response genes. Science. 2013 Aug 16;341(6147):789-92.[3]Long noncoding RNA expression profile in fibroblast-like synoviocytes from patients with rheumatoid arthritis. Arthritis Res Ther. 2016 Oct 6;18(1):227.Disclosure of Interests:None declared


2014 ◽  
Vol 50 ◽  
pp. 59-66 ◽  
Author(s):  
Sinisa Savic ◽  
Lylia Ouboussad ◽  
Laura J. Dickie ◽  
Janina Geiler ◽  
Chi Wong ◽  
...  

2014 ◽  
Vol 73 (Suppl 1) ◽  
pp. A8.1-A8
Author(s):  
Paola Bonaventura ◽  
Fabien Lavocat ◽  
Giulia Benedetti ◽  
Aline Lambroux ◽  
Francis Albarede ◽  
...  

2002 ◽  
Vol 46 (11) ◽  
pp. 2867-2877 ◽  
Author(s):  
Malini Sen ◽  
Jack Reifert ◽  
Kevin Lauterbach ◽  
Vladimir Wolf ◽  
Jeffrey S. Rubin ◽  
...  

Fitoterapia ◽  
2019 ◽  
Vol 139 ◽  
pp. 104402 ◽  
Author(s):  
Anna Jesionek ◽  
Adam Kokotkiewicz ◽  
Anna Mikosik-Roczynska ◽  
Klaudia Ciesielska-Figlon ◽  
Piotr Luczkiewicz ◽  
...  

2015 ◽  
Vol 2015 ◽  
pp. 1-10 ◽  
Author(s):  
Geng Yin ◽  
Ying Wang ◽  
Xiao-min Cen ◽  
Min Yang ◽  
Yan Liang ◽  
...  

Rheumatoid arthritis (RA) is a systemic autoimmune disease characterized by chronic inflammation of multiple joints. The central pathogenesis of RA is the proliferation of synovial fibroblasts in response to inflammatory cytokines. However, some of the targeted therapies for inflammation reactions do not display significant clinical improvement after initiation of therapy. Thus, the relationship between inflammatory responses and RA therapy is still incompletely understood. In the present study, we proposed to determine whether enhanced inflammations may lead to cell apoptosis in rheumatoid arthritis synoviocytes. Our results indicated that products of lipid peroxidations, 4-HNE, may induce synovial intrinsic inflammations by activating NF-κB pathways and it may lead to cell apoptosis. Pharmacological inhibition of NF-κB activation may reduce the 4-HNE mediated inflammation responses and subsequent cell apoptosis. Our results may help to clarify the role of inflammations on RA development and imply that blocking NF-κB activation may be partly beneficial for human RA therapy. These findings might provide a mechanism-based rationale for developing new strategy to RA clinical therapy.


1996 ◽  
Vol 39 (1) ◽  
pp. 125-136 ◽  
Author(s):  
Carlene Tsai ◽  
Luis A. Diaz ◽  
Nora G. Singer ◽  
Lan Lan Li ◽  
Anita H. Kirsch ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document