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Semi-vioxanthin isolated from marine-derived fungus regulates tumor necrosis factor-alpha, cluster of differentiation (CD) 80, CD86, and major histocompatibility complex class II expression in RAW264.7 cells via nuclear factor-kappaB and mitogen-activated protein kinase signaling pathways

Semi-vioxanthin isolated from marine-derived fungus was assessed for immunoregulatory activity in mouse RAW264.7 macrophages. In the present study, the facilitative effects of semi-vioxanthin on tumor necrosis factor-alpha (TNF-alpha) and its mRNA expression and on expression of the co-stimulatory m...

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Published in:Biological & pharmaceutical bulletin 2008, Vol.31 (12), p.2228-2233
Main Authors: Yang, Xin-Ying, Cai, Sheng-Xin, Zhang, Wen-Ji, Tang, Xue-Lian, Shin, Hye-Young, Lee, Joo-Young, Gu, Qian-Qun, Park, Hyun
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container_title Biological & pharmaceutical bulletin
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creator Yang, Xin-Ying
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description Semi-vioxanthin isolated from marine-derived fungus was assessed for immunoregulatory activity in mouse RAW264.7 macrophages. In the present study, the facilitative effects of semi-vioxanthin on tumor necrosis factor-alpha (TNF-alpha) and its mRNA expression and on expression of the co-stimulatory molecules, cluster of differentiation (CD) 80, CD86 and major histocompatibility complex class II (MHC II), as well as the molecular mechanism underlying the immunologic enhancement properties of semi-vioxanthin were studied. Our results clearly indicated that semi-vioxanthin treatment resulted in the degradation of IkappaB alpha, which led to the activation and nuclear translocation of the p65 subunit of nuclear factor-kappaB (NF-kappaB), as determined by immunoblotting, immunofluorescence and electrophoretic mobility shift assays (EMSA). Moreover, TNF-alpha production was prevented by NF-kappaB and mitogen-activated protein kinase (MAPK) inhibitors. Inhibition of NF-kappaB and extracellular signal regulated kinases (ERK1/2) activity by specific inhibitors blunted the effect of semi-vioxanthin on the up-regulation of CD80, CD86 and MHCII expression, but neither p38 MAPK nor c-Jun N-terminal kinase (JNK) inhibitor had this effect. Thus, we demonstrate that semi-vioxanthin regulates TNF-alpha production through NF-kappaB and MAPK signaling pathways. Activation of NF-kappaB and ERK1/2 were necessary for CD80, CD86 and MHCII expression induced by semi-vioxanthin. These data suggest that semi-vioxanthin has immunoregulatory effects.
doi_str_mv 10.1248/bpb.31.2228
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pharmaceutical bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Xin-Ying</au><au>Cai, Sheng-Xin</au><au>Zhang, Wen-Ji</au><au>Tang, Xue-Lian</au><au>Shin, Hye-Young</au><au>Lee, Joo-Young</au><au>Gu, Qian-Qun</au><au>Park, Hyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Semi-vioxanthin isolated from marine-derived fungus regulates tumor necrosis factor-alpha, cluster of differentiation (CD) 80, CD86, and major histocompatibility complex class II expression in RAW264.7 cells via nuclear factor-kappaB and mitogen-activated protein kinase signaling pathways</atitle><jtitle>Biological &amp; pharmaceutical bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2008</date><risdate>2008</risdate><volume>31</volume><issue>12</issue><spage>2228</spage><epage>2233</epage><pages>2228-2233</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>Semi-vioxanthin isolated from marine-derived fungus was assessed for immunoregulatory activity in mouse RAW264.7 macrophages. In the present study, the facilitative effects of semi-vioxanthin on tumor necrosis factor-alpha (TNF-alpha) and its mRNA expression and on expression of the co-stimulatory molecules, cluster of differentiation (CD) 80, CD86 and major histocompatibility complex class II (MHC II), as well as the molecular mechanism underlying the immunologic enhancement properties of semi-vioxanthin were studied. Our results clearly indicated that semi-vioxanthin treatment resulted in the degradation of IkappaB alpha, which led to the activation and nuclear translocation of the p65 subunit of nuclear factor-kappaB (NF-kappaB), as determined by immunoblotting, immunofluorescence and electrophoretic mobility shift assays (EMSA). Moreover, TNF-alpha production was prevented by NF-kappaB and mitogen-activated protein kinase (MAPK) inhibitors. Inhibition of NF-kappaB and extracellular signal regulated kinases (ERK1/2) activity by specific inhibitors blunted the effect of semi-vioxanthin on the up-regulation of CD80, CD86 and MHCII expression, but neither p38 MAPK nor c-Jun N-terminal kinase (JNK) inhibitor had this effect. Thus, we demonstrate that semi-vioxanthin regulates TNF-alpha production through NF-kappaB and MAPK signaling pathways. Activation of NF-kappaB and ERK1/2 were necessary for CD80, CD86 and MHCII expression induced by semi-vioxanthin. These data suggest that semi-vioxanthin has immunoregulatory effects.</abstract><cop>Japan</cop><pmid>19043204</pmid><doi>10.1248/bpb.31.2228</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Animals
B7-1 Antigen - biosynthesis
B7-1 Antigen - genetics
B7-2 Antigen - biosynthesis
B7-2 Antigen - genetics
Blotting, Western
Cell Line
Electrophoretic Mobility Shift Assay
Flow Cytometry
Fluorescent Antibody Technique
Gene Expression - drug effects
Genes, MHC Class II - genetics
Macrophages - drug effects
Macrophages - metabolism
Macrophages - physiology
Mice
Mitogen-Activated Protein Kinases - genetics
Mitogen-Activated Protein Kinases - physiology
Naphthols - isolation & purification
Naphthols - pharmacology
NF-kappa B - genetics
NF-kappa B - physiology
Pyrones - isolation & purification
Pyrones - pharmacology
Reverse Transcriptase Polymerase Chain Reaction
RNA - biosynthesis
RNA - genetics
Signal Transduction - physiology
Tumor Necrosis Factor-alpha - biosynthesis
Tumor Necrosis Factor-alpha - genetics
Up-Regulation - drug effects
title Semi-vioxanthin isolated from marine-derived fungus regulates tumor necrosis factor-alpha, cluster of differentiation (CD) 80, CD86, and major histocompatibility complex class II expression in RAW264.7 cells via nuclear factor-kappaB and mitogen-activated protein kinase signaling pathways
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