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   The amelioration of phagocytic ability in microglial cells by curcumin through the inhibition of EMF-induced pro-inflammatory responses  
   
نویسنده he g.-l. ,liu y. ,li m. ,chen c.-h. ,gao p. ,yu z.-p. ,yang x.-s.
منبع journal of neuroinflammation - 2014 - دوره : 11 - شماره : 0
چکیده    Background: insufficient clearance by microglial cells,prevalent in several neurological conditions and diseases,is intricately intertwined with mfg-e8 expression and inflammatory responses. electromagnetic field (emf) exposure can elicit the pro-inflammatory activation and may also trigger an alteration of the clearance function in microglial cells. curcumin has important roles in the anti-inflammatory and phagocytic process. here,we evaluated the ability of curcumin to ameliorate the phagocytic ability of emf-exposed microglial cells (n9 cells) and documented relative pathways.methods: n9 cells were pretreated with or without recombinant murine mfg-e8 (rmmfg-e8),curcumin and an antibody of toll-like receptor 4 (anti-tlr4),and subsequently treated with emf or a sham exposure. their phagocytic ability was evaluated using phosphatidylserine-containing fluorescent bioparticles. the pro-inflammatory activation of microglia was assessed via cd11b immunoreactivity and the production of tumor necrosis factor-α (tnf-α),interleukin-6 (il-6),interleukin-1β (il-1β) and nitric oxide (no) via the enzyme-linked immunosorbent assay or the griess test. we evaluated the ability of curcumin to ameliorate the phagocytic ability of emf-exposed n9 cells,including checking the expression of mfg-e8,αvβ3 integrin,tlr4,nuclear factor-κb (nf-κb) and signal transducer and activator of transcription 3 (stat3) using western blotting.results: emf exposure dramatically enhanced the expression of cd11b and depressed the phagocytic ability of n9 cells. rmmfg-e8 could clearly ameliorate the phagocytic ability of n9 cells after emf exposure. we also found that emf exposure significantly increased the secretion of pro-inflammatory cytokines (tnf-α,il-6 and il-1β) and the production of no; however,these increases were efficiently chilled by the addition of curcumin to the culture medium. this reduction led to the amelioration of the phagocytic ability of emf-exposed n9 cells. western blot analysis revealed that curcumin and naloxone restored the expression of mfg-e8 but had no effect on tlr4 and cytosolic stat3. moreover,curcumin significantly reduced the expression of nf-κb p65 in nuclei and phospho-stat3 (p-stat3) in cytosols and nuclei.conclusions: this study indicates that curcumin ameliorates the depressed mfg-e8 expression and the attenuated phagocytic ability of emf-exposed n9 cells,which is attributable to the inhibition of the pro-inflammatory response through the nf-κb and stat3 pathways. © 2014 he et al.; licensee biomed central ltd.
آدرس key laboratory of medical protection for electromagnetic radiation ministry of education,third military medical university,30 gaotanyan street,chongqing 400038,china,institute of tropical medicine,third military medical university,chongqing 400038, China, southwest eye hospital,southwest hospital,third military medical university,chongqing 400038, China, key laboratory of medical protection for electromagnetic radiation ministry of education,third military medical university,30 gaotanyan street,chongqing 400038, China, key laboratory of medical protection for electromagnetic radiation ministry of education,third military medical university,30 gaotanyan street,chongqing 400038, China, key laboratory of medical protection for electromagnetic radiation ministry of education,third military medical university,30 gaotanyan street,chongqing 400038, China, key laboratory of medical protection for electromagnetic radiation ministry of education,third military medical university,30 gaotanyan street,chongqing 400038, China, key laboratory of medical protection for electromagnetic radiation ministry of education,third military medical university,30 gaotanyan street,chongqing 400038,china,institute of tropical medicine,third military medical university,chongqing 400038, China
 
     
   
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