Author/Authors :
Liu، نويسنده , , Junhong and Hong، نويسنده , , Suli and Feng، نويسنده , , Zhiyong and Xin، نويسنده , , Yinqiang and Wang، نويسنده , , Qi and Fu، نويسنده , , Jin and Zhang، نويسنده , , Chao and Li، نويسنده , , Guilan and Luo، نويسنده , , Lan and Yin، نويسنده , , Zhimin، نويسنده ,
Abstract :
HSP27 is a member of the small HSP family which has been linked to different signaling pathways regulating critical cellular functions. But the role of HSP27 in LPS-induced inflammatory signaling pathways is still unclear. In the present study, both overexpression and RNA interference experiments indicated that HSP27 increased LPS-induced expression of iNOS and COX-2 and release of NO/PGE2 through enhancing NF-κB but not MAPK activation. The effects of HSP27 on LPS-induced iNOS/COX-2 expression and relative signaling cascade were closely related with the phosphorylation of HSP27. Further studies have shown that HSP27-regulated LPS-induced activation of NF-κB by interacting with TRAF6 and increasing the association of TRAF6-IKKγ. This could be a probable mechanism by which HSP27 modulates LPS-induce inflammatory signaling pathways. Thus, HSP27 may play a potential role in regulating inflammatory responses in immunologic system.
Keywords :
hsp27 , TRAF6 , LPS , COX-2 , NF-?B , iNOS