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PI3K/Akt pathway is involved in the activation of RAW 264.7 cells induced by hydroxypropyltrimethyl ammonium chloride chitosan
作者姓名:YANG Yue  XING Rong’e  LIU Song  QIN Yukun  LI Kecheng  YU Huahua  LI Pengcheng
作者单位:Key Laboratory of Experimental Marine Biology;Laboratory for Marine Drugs and Bioproducts of Qingdao National Laboratory for Marine Science and Technology;University of Chinese Academy of Sciences
基金项目:Supported by the National Key R&D Program of China(No.2018YFC0311305);the Key Research and Development Program of Shandong Province(Nos.2019GHY112015,2019YYSP028)。
摘    要:We previously demonstrated that 2-hydroxypropyltrimethyl ammonium chloride chitosan(HACC)promoted the production of nitric oxide(NO)and proinflammatory cytokines by activating the mitogen-activated protein kinases(MAPK)and Janus kinase(JAK)/STAT pathways in RAW 264.7 cells,indicating good immunomodulatory activity of HACC.In this study,to further investigate the immunomodulatory mechanisms of HACC,we determined the roles of phosphatidylinositol 3-kinase(PI3K)/Akt,activating protein(AP-1)and nuclear factor kappa B(NF-κB)in HACC-induced activation of RAW 264.7 cells by the western blotting.The results suggest that HACC promoted the phosphorylation of p85 and Akt.Furthermore,c-Jun and p65 were also increased after the treatment of RAW 264.7 cells with HACC,indicating the translocation of NF-κB and AP-1 from cytoplasm to nucleus.In addition,as scanning electron microscopy(SEM)analysis shows,the cell morphology changed after HACC treatment.These findings indicate that HACC activated MAPK,JAK/STAT,and PI3K/Akt signaling pathways dependent on AP-1 and NF-κB activation in RAW 264.7 cells,ultimately leading to the increase of NO and cytokines.

关 键 词:hydroxypropyltrimethyl  AMMONIUM  chloride  CHITOSAN  RAW  264.7  CELLS  PI3K/Akt  pathway  nuclear  factor-κB  ACTIVATING  protein  1
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