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Projects

Participation of DC-STAMP in Inflammatory Arthritis

Participation of DC-STAMP in Inflammatory ArthritisBone remodeling is a dynamic and complex process finely orchestrated by cell interactions among osteoblast, T, B and natural killer cells. The first phase of bone remodeling requires activation of monocytes/macrophages by M-CSF and the receptor activator nuclear factor-kappa B ligand (RANKL) to initiate cell-cell contact and induce the formation of multinucleated osteoclasts (OCs).

DC-STAMP, a transmembrane protein, is essential at early stages of cell-cell fusion and OC differentiation. Although osteoclast precursors lacking DC-STAMP form mononuclear osteoclasts (mOCs) in vitro, they are still able to dissolve bone. Despite DC-STAMP being expressed in different cell types including dendritic cells, T cells, mononuclear and stromal cells, there are scarce studies showing its role in the immune response. Thus, the focus our laboratory is to:

  1. Elucidate the contribution of DC-STAMP in bone remodeling in TNF Tg and K/BxN mice, two inflammatory arthritis models
  2. Evaluate the therapeutic effect of neutralizing DC-STAMP antibodies in a humanized mouse model of rheumatoid arthritis and psoriatic arthritis
  3. Investigate whether DC-STAMP modulates tumor immunity using a mouse melanoma model.

Our main goal is to underline the cellular and molecular pathways that are affected by DC-STAMP expression and/or activation during the onset of RA in TNF Tg and NODxKRN mouse model. We recently showed that the absence of DC-STAMP in TNF Tg mouse model decreases bone resorption and migration of osteoclast precursors to inflamed synovium.

TNF Tg mice show visibly swollen jointsAnkle thickness, TNF Tg mice vs DC-STAMP-/-x TNF Tg micePercentage of TRAP+ area, TNF Tg mice vs DC-STAMP-/-x TNF Tg mice

Bone density, TNF Tg mice and DC-STAMP-/-x TNF Tg mice

Figure Legend. The absence of DC-STAMP ameliorates RA in TNF Tg mice.
TNF Tg mice show visibly swollen joints (A-left panels), accumulation of TRAP+ osteoclasts, considerable inflammatory cell infiltration and cartilage damage (A-right panels) compared with DC-STAMP-/-x TNF Tg mice, which correlate with a significant increase of ankle thickness (B), higher percentage of TRAP+ area(C), and low bone density (D). Representative results of 5-month old TNF Tg and DC-STAMP-/-x TNF Tg mice are shown.