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A8.14 The Anti-Proliferative Function of RSK2 in Synovial Fibroblasts Protects Against TNF-α-Induced Joint Destruction in Inflammatory Arthritis
  1. Anja Derer1,*,
  2. Christina Böhm1,*,
  3. Bettina Herbort1,
  4. Sybille Böhm2,
  5. Kirsten Neubert3,
  6. Michael Stock1,
  7. Christine Zech1,
  8. Georg Schett1,
  9. Axel J Hueber1,*,
  10. Jean-Pierre David1,4,*
  1. 1Department of Internal Medicine 3, Rheumatology and Immunology, University Hospital, Erlangen, Germany
  2. 2Department of Biology, University of Erlangen-Nuremberg
  3. 3Department of Dermatology, Research Modul II, University Hospital, Erlangen
  4. 4Institute for Osteology and Biomechanics, University Medical Center Hamburg-Eppendorf, Hamburg, Germany,


Background/Objectives The pro-inflammatory cytokine Tumor Necrosis Factor alpha (TNF-α) directly activates the ribosomal S6 kinase RSK2 in vitro. We recently demonstrated the protective effect of RSK2 against TNF-induced bone loss. Interestingly, we found an increased activation of RSK2 in the joints of arthritis patients as well as in the inflamed joints of mice overexpressing the human TNF-α (hTNFtg). These observations prompted us to investigate the function of RSK2 in the development of TNF-α-induced inflammatory arthritis.

Materials and Methods hTNFtg mice were crossed with RSK2-deficient (Rsk2y/-) mice. Clinical scoring and histomorphometry of the joints were assessed. We compared the levels of circulating pro-inflammatory cytokines as well as the cellularity of myeloid lineages in the spleen. The expression of cytokines and mesenchymal markers in the joints was determined via QPCR. Bone marrow transfer of Rsk2y/- and wild-type littermates into hTNFtg mice was performed and clinical scoring as well as histomorphometry of the joints was assessed. Primary fibroblast-like synoviocytes (FLS) from hTNFtg and hTNFtg; Rsk2y/ mice were isolated to analyse their expression of inflammatory cytokines and metalloproteinases as well as their proliferation and apoptosis in vitro.

Results RSK2 deficiency in hTNFtg mice resulted in an early onset of clinical signs of arthritis as well as a drastic exacerbation of inflammation, increased cartilage destruction and increased local bone destruction. Increased levels of circulating pro-inflammatory cytokines and the increased proportion of all myeloid lineages in the spleen confirmed the enhanced inflammation in the hTNFtg mice lacking RSK2. Increased activation of synovial fibroblasts and macrophages in the joints of hTNFtg; Rsk2 y/- mice was demonstrated by the locally increased expression of pro-inflammatory cytokines and matrix metalloproteinases (MMPs). Importantly, the phenotype could not be transmitted by the transfer of Rsk2 y/- bone marrow into hTNFtg mice that demonstrated the essential role for RSK2 expression in mesenchymal cells driving the pathogenesis. In agreement, although no difference in the expression of pro-inflammatory cytokines or MMPs nor a change in apoptosis was detected in synovial fibroblasts isolated from hTNFtg; Rsk2 y/- , these cells displayed an increased proliferation rate.

Conclusions The anti-proliferative function of RSK2 controls a cell autonomous negative feed-back against the activation of synovial fibroblasts by TNF-α, therefore limiting joint destruction in arthritis. Thus, activation of RSK2 is a potential target for the treatment of both local and systemic bone destruction in RA.

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