Kawana Hidetada, Karaki Hirokazu, Higashi Morihiro, Miyazaki Masaru, Hilberg Frank, Kitagawa Motoo, Harigaya Kenichi
Department of Molecular and Tumor Pathology, Chiba University Graduate School of Medicine, Inohana, Chuo-ku, Chiba, Japan.
J Immunol. 2008 Mar 15;180(6):4235-45. doi: 10.4049/jimmunol.180.6.4235.
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.
细胞粘附分子CD44是主要的透明质酸受体,与透明质酸的结合、内吞作用及代谢有关。以往研究表明,CD44在多种炎症性疾病中起关键作用。近年来,Toll样受体(TLRs)作为古老的微生物模式识别受体,已被证明可启动先天性免疫反应,并与多种炎症性疾病相关。本研究表明,CD44通过激活NF-κB对TLRs介导的体内炎症起负调节作用,这会导致促炎细胞因子的产生。此外,我们的结果显示,当受到TLR2配体酵母聚糖刺激时,CD44直接与TLR2结合,且CD44的胞质结构域对其对TLR信号的调节作用至关重要。本研究表明,CD44在TLR介导的炎症中起保护作用,并且首次证明了CD44与TLR之间存在直接关联。