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Publication : CD44 suppresses TLR-mediated inflammation.

First Author  Kawana H Year  2008
Journal  J Immunol Volume  180
Issue  6 Pages  4235-45
PubMed ID  18322236 Mgi Jnum  J:132955
Mgi Id  MGI:3777232 Doi  10.4049/jimmunol.180.6.4235
Citation  Kawana H, et al. (2008) CD44 Suppresses TLR-Mediated Inflammation. J Immunol 180(6):4235-45
abstractText  The cell adhesion molecule CD44, which is the major hyaluronan receptor, has been implicated in the binding, endocytosis, and metabolism of hyaluronan. Previous studies have revealed that CD44 plays crucial roles in a variety of inflammatory diseases. In recent years, TLRs, which are ancient microbial pattern recognition receptors, have been shown to initiate an innate immune response and have been linked to a variety of inflammatory diseases. The present study shows that CD44 negatively regulates in vivo inflammation mediated by TLRs via NF-kappaB activation, which leads to proinflammatory cytokine production. Furthermore, our results show that CD44 directly associates with TLR2 when stimulated by the TLR2 ligand zymosan and that the cytoplasmic domain of CD44 is crucial for its regulatory effect on TLR signaling. This study indicates that CD44 plays a protective role in TLR-mediated inflammation and is the first to demonstrate a direct association between CD44 and a TLR.
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