Journal article
Catabolic cytokines disrupt the circadian clock and the expression of clock-controlled genes in cartilage via an NFkB-dependent pathway
B Guo, N Yang, E Borysiewicz, M Dudek, JL Williams, J Li, ES Maywood, A Adamson, MH Hastings, JF Bateman, MRH White, RP Boot-Handford, QJ Meng
Osteoarthritis and Cartilage | ELSEVIER SCI LTD | Published : 2015
Abstract
Objective: To define how the catabolic cytokines (Interleukin 1 (IL-1) and tumor necrosis factor alpha (TNFα)) affect the circadian clock mechanism and the expression of clock-controlled catabolic genes within cartilage, and to identify the downstream pathways linking the cytokines to the molecular clock within chondrocytes. Methods: Ex vivo cartilage explants were isolated from the Cry1-luc or PER2::LUC clock reporter mice. Clock gene dynamics were monitored in real-time by bioluminescence photon counting. Gene expression changes were studied by qRT-PCR. Functional luc assays were used to study the function of the core Clock/BMAL1 complex in SW-1353 cells. NFkB pathway inhibitor and fluores..
View full abstractGrants
Awarded by European Commission
Funding Acknowledgements
This work has been funded by the following grants: a Medical Research Council (MRC) Career Development Award (G0900414 to QJM), a MRC grant (MR/K019392/1 to QJM and RPBH). MRW is funded by a BBSRC SABR (BB/F005938/2) and sLOLA (BB/K003097/1), a MRC (MR/K015885/1) and an EU FP7 (FP7/305564) grant. JL is funded by the National Natural Science Foundation of China (81450044, 81171253 and 31200889). We thank Dr. Dharshika Pathiranage for technical support.