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A9.17 Targeting the Expression of miR-146a in Mouse Inflammatory Ly6Chigh Monocyte Subset for Therapeutic Intervention in Arthritis
  1. M Ammari1,2,
  2. I Duroux-Richard1,2,
  3. J Presumey1,2,
  4. C Roubert3,
  5. V Escriou4,5,
  6. C Jorgensen1,2,6,
  7. F Apparailly1,2,6
  1. 1Inserm, U 844, 80 rue Augustin Fliche, F-34295 Montpellier, France
  2. 2University of Medicine, F-34000 Montpellier, France
  3. 3Exploratory Unit, Sanofi-Aventis R & D, 371 rue du professeur J Blayac, 34184 Montpellier, France
  4. 4Inserm, U 1022, UFR des Sciences Pharmaceutiques et Biologiques; 4Avenue de l’Observatoire, 75006 Paris, France
  5. 5CNRS, UMR8151, 75006 Paris, France
  6. 6University hospital of Montpellier, clinical unit for osteoarticular diseases, F-34295 Montpellier, France

Abstract

Background and Objectives Monocytes can give rise to different cell types including osteoclasts (OC), which play an important role in maintaining bone homeostasis by resorbing bone matrix. Circulating monocytes consist of at least two main functional subsets of immune cells, Ly6Chigh and Ly6Clow monocytes, arising from a common progenitor in the bone marrow. Excessive and prolonged activation of inflammatory LyC6high monocytes is a hallmark of many inflammatory diseases including arthritis. Among key molecular rheostats, micro (mi) RNAs are a class of regulatory RNAs that control basic biological functions and orchestrate inflammatory responses. Among master miRNAs of innate immunity, miR-146a exerts a negative retro-control on inflammation transduction signals and inhibits osteoclastogenesis. Despite aberrant increased expression in rheumatoid arthritis (RA), miR-146a is unable to properly down regulate inflammation, leading to prolonged TNF production and increased OC, two arthritis hallmarks. Here, we investigated whether miR-146a was differentially regulated in both Ly6Chigh and Ly6Clow monocyte subsets in healthy and arthritic conditions. Moreover, we developed techniques to deliver siRNA to LyC6high monocytes in vivo and thus determined the specific impact of miR-146a overexpression in this particular monocyte subset on inflammation and osteoclastogenesis, in the context of arthritis.

Materials and Methods Subset monocytes were isolated from peripheral blood of arthritic and healthy mice by FACS sorting following membrane stainings. Transcriptomic analyses for miRNA expression were performed (n = 6) and differential miRNA expression levels were validated on individual samples using multiplex RT-qPCR (n = 13). Collagen-induced arthritic (CIA) mice were injected intravenously at disease onset with lipoplex containing either control or miR-146a mimic (0.5 mg/kg). Arthritis severity was monitored and OC differentiation was performed by stimulating bone marrow-derived monocytes (BMDM) with M-CSF and RANK-L miR-146a expression levels measured during OC differentiation. TRAP activity, OC numbers and nuclei per OC were quantified.

Results Transcriptomic analyses showed higher expression of miR-146a in Ly6Clow monocytes when compared to Ly6Chigh monocytes, in both healthy and arthritis mice. In arthritis mice, expression of miR-146a in Ly6Chigh monocytes is down-regulated as compared to healthy controls. During differentiation of BMDM into OC, miR-146a expression levels are down-regulated on day 2. Enforced expression of miR-146a in Ly6Chigh monocytes upon intravenous injection of miR-146a-containing lipoplex leads to decreased bone erosion in mouse CIA. This effect was associated with a decreased number of mature OC and TRAP activity, as well as a reduced number of nuclei per OC.

Conclusions Overall, our results show that specific over-expression of miR-146a in Ly6Chigh monocytes alters OC differentiation and decreased bone erosion in mouse CIA. These data also suggest that Ly6Chigh monocytes might be the monocyte subset precursor of OC, and that targeting this specific monocyte subset might represent a therapeutic option in the context of arthritis to inhibit bone loss.

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