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My laboratory is interested in the role cell-matrix interactions play in tissue homeostasis. In particular, our research has focused on cell-matrix interactions that relate to the matrix macromolecule hyaluronan. Changes in hyaluronan metabolism may underlie the cartilage degeneration associated with osteoarthritis. To better understand the metabolism of hyaluronan in cartilage, we have focused on the enzymes that synthesize hyaluronan (hyaluronan synthases), cellular hyaluronidases and, the principal hyaluronan receptor, CD44. We were the first laboratory to identify HAS2 as the primary hyaluronan synthase used by articular chondrocytes. We have cloned two of three critical lysosomal hyaluronidases HYAL1, HYAL2, examined their function and distribution, inhibited their expression by siRNA and antisense and, characterized the promoter of region of the HYAL2 hyaluronidase. We have shown that changes in CD44 receptor occupancy in chondrocytes affect signaling events such as p38 MAPK pathways and NF-kB resulting in increases in the matrix metalloproteinases, MMP-3 and MMP-13 as well as ADAMTS-4 and ADAMTS-5. We have also demonstrated the role of CD44 as an endocytosis receptor for hyaluronan and have generated point mutations within full length CD44 that block internalization but do interfere with hyaluronan binding. We have determined that the internalization of aggrecan G1 domains that remain bound to hyaluronan after aggrecanolysis require CD44. CD44 expression was knocked down by siRNA or function by CD44-DN. Both approaches prevented the retention and internalization of G1-ITEGE. Inhibition of CD44 transit into lipid rafts blocked the endocytosis of G1-ITEGE but not the retention at the cell surface. Additionally, chondrocytes or fibroblasts derived from Cd44-/- mice exhibited little capacity for retention and internalization of exogenous G1-ITEGE. The consequence of a lack of chondrocyte-mediated endocytosis of these domains in cartilage of the CD44 null mice was the accumulation of the degradation fragments within the tissue. Our current work focuses on the transfer of HAS and CD44 transgenes into cartilage and chondrocytes. These strategies allow us to elucidate the functional role of hyaluronan and CD44 in maintaining cartilage homeostasis. Quite unexpectedly however, we recently determined that overexpression of HAS2 transgenes into osteoarthritic chondrocytes did more that affect hyaluronan levels but rather, resulted in the reversion of an aberrant energy metabolism of these cells, due in part to shifts in usage of UDP-GlcUA and UDP-GlcNAc precursors. We identified other agents that provide the same anti-catabolic, anti-inflammatory effects as HAS2 overexpression which led us to define new intriguing mechanisms on how to limit the effects of osteoarthritis by manipulating metabolism. Moreover one of our agents, namely 4-methyumbelliferone, successfully blocked osteoarthritis in vivo in mice following medial meniscus transection.
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