Smolinska, Maria J, Page, Theresa H, Urbaniak, Ania M, Mutch, Brenda E and Horwood, Nicole J ORCID: https://orcid.org/0000-0002-6344-1677
(2011)
Hck tyrosine kinase regulates TLR4-induced TNF and IL-6 production via AP-1.
Journal of Immunology, 187 (11).
pp. 6043-6051.
ISSN 0022-1767
Abstract
The TLRs play a key role in host defense against infection and injury, and mounting evidence suggests that these receptors may also play a role in diseases such autoimmunity, atherosclerosis, and cancer. Activation of TLRs on macrophages results in the production of multiple soluble mediators including the key inflammatory cytokines, TNF and IL-6. Thus, the intracellular signaling mechanism by which TLRs signal is a subject of great interest. As well as activating the NF-κB and MAPK pathways, TLR engagement leads to tyrosine kinase activation within minutes. Src family kinases (SFKs) are the largest nonreceptor tyrosine kinase family with nine members: Src, Hck, Lyn, Fyn, Fgr, Blk, Lck, Yes, and Ylk. The role of the SFKs in TLR signaling has been an area of much controversy, with conflicting findings between studies using chemical inhibitors and knockout mice. Using primary human macrophages in combination with adenoviral overexpression and small interfering RNA knockdown studies, we show that the SFK, Hck, has a pre-eminent role in LPS/TLR4-induced TNF and IL-6 production. Hck kinase mediates TLR4-induced transcription of both TNF and IL-6 by a mechanism that involves neither the NF-κB nor the MAPK pathways, but rather leads to AP-1 binding with a complex of c-fos and JunD. These data highlight the importance of Hck as an active component in LPS-induced TLR signaling and suggest the possibility of targeting this kinase for the alleviation of excessive inflammation.
Item Type: | Article |
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Uncontrolled Keywords: | blotting, western,cells, cultured,electrophoretic mobility shift assay,enzyme-linked immunosorbent assay,genetics,genetics,humans,biosynthesis,immunology,genetics,rna interference,real-time polymerase chain reaction,immunology,genetics,genetics,biosynthesis,sdg 3 - good health and well-being ,/dk/atira/pure/sustainabledevelopmentgoals/good_health_and_well_being |
Faculty \ School: | Faculty of Medicine and Health Sciences > Norwich Medical School |
UEA Research Groups: | Faculty of Medicine and Health Sciences > Research Centres > Metabolic Health |
Depositing User: | LivePure Connector |
Date Deposited: | 06 Mar 2019 10:30 |
Last Modified: | 24 Jul 2024 09:49 |
URI: | https://ueaeprints.uea.ac.uk/id/eprint/70141 |
DOI: | 10.4049/jimmunol.1100967 |
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