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    Please use this identifier to cite or link to this item: http://ir.cnu.edu.tw/handle/310902800/32176


    標題: Importance of PLC-Dependent PI3K/AKT and AMPK Signaling in RANTES/CCR5 Mediated Macrophage Chemotaxis
    作者: Chien, Hung-Che
    Chan, Pei-Chi
    Tu, Chuan-Chou
    Day, Yuan-Ji
    Hung, Li-Man
    Juan, Chi-Chang
    Tian, Yu-Feng
    Hsieh, Po-Shiuan
    貢獻者: Natl Def Med Ctr, Dept Physiol & Biophys
    Armed Forces Taichung Gen Hosp, Dept Internal Med
    Chang Gung Mem Hosp, Dept Anesthesia
    Chang Gang Univ, Coll Med, Dept & Grad Inst Biomed Sci
    Chang Gang Univ, Coll Med, Hlth Aging Res Ctr
    Natl Yang Ming Univ, Sch Med, Inst Physiol
    Chi Mei Med Ctr, Div Gen Surg, Dept Surg, Yung Kung Campus
    Chia Nan Univ Pharm & Sci
    Natl Def Med Ctr, Inst Prevent Med
    Triserv Gen Hosp, Dept Med Res
    關鍵字: CCR5
    macrophage chemotaxis
    phospholipase C
    RANTES
    日期: 2018-10-31
    上傳時間: 2019-11-15 15:43:51 (UTC+8)
    出版者: CHINESE PHYSIOLOGICAL SOC
    摘要: Regulated upon activation, normal T cell expressed, and secreted (RANTES), also known as chemokine ligand 5 (CCL5), has been reported to facilitate macrophage migration, which plays a crucial role in tissue inflammation. The aim of this study is to investigate the characteristics and underlying mechanism of RANTES on macrophage chemotaxis under physiological and pathological conditions. The study was conducted on macrophage RAW264.7 cell and bone marrow-derived macrophages (BNIDM) isolated from CCL receptor 5 (CCR5) knockout mice. The macrophage migration and glucose uptake was assessed in time and dose dependent manners. Moreover, reverse transcription-polymerase chain reaction (RT-PCR) and western blot analysis were used to characterize mRNA and protein level related to the underlying mechanism. The present result showed that the maraviroc, a selective CCR5 inhibitor, dose-dependently suppressed RANTES-induced rapid increases in glucose uptake and cell migration in RAW264.7 cells. Similar effects were observed in the BMDM isolated from CCR5 knockout mice compared with wild type control. RANTES treatment promptly enhanced membrane glucose transporter 1 (GLUT1) expression, glucose uptake as well as phosphorylation of AKT on Thr308, Ser473 within min and has prolonged effect on phosphorylation of AMP-activated protein kinase (AMPK) on Thr172, which were abrogated by maraviroc, CCR5 siRNA or phospholipase C (PLC) inhibitor in RAW264.7 cells. Inhibition of PI3K and AMPK by LY294002 and Compound C significantly suppress RANTES-stimulated macrophage glucose uptake and migration, respectively. RANTES has biphasic effect on activating PLC signaling including prompt action on PI3K/AKT phosphorylation and prolong action on AMPK phosphorylation via CCR5 which leads to increased GLUT1-mediated glucose uptake and macrophage migration under physiopathological states.
    link: http://dx.doi.org/10.4077/CJP.2018.BAG584
    關聯: Infection and Drug Resistance, v.61, n.5, pp.266-279
    Appears in Collections:[保健營養系(所) ] 期刊論文

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