Objective: To study the effects of PAF, in comparison with OxLDL and IL-1 beta on MCP-1 and IL-6 secretion from U-937 monocytes and to investigate the mechanism of its action. Methods: U-937 cell line was cultured in the presence or absence of PAF or OxLDL or IL-1 beta. Secretion of IL-6 and MCP-1 was measured by ELISA method, mRNA levels of MCP-1 and PAFR was measured using real-time PCR. In order to investigate the mechanism of mediator's action signal transduction appropriate inhibitors was used and oxidant status of cells by measurement the total cellular thiols content and glutathione was determined. Results and conclusion: None of the tested mediators induced the secretion of IL-6. On the other hand PAF and OxLDL caused a short-term while IL-1 beta caused a long-term secretion and expression of MCP-1. Reduced total thiol levels and GSH/GSSG ratio indicate that the above mediators induce oxidative stress. The signal transduction of all mediators is mediated through G-proteins, protein kinases (PKC, serine-threonine kinase and tyrosine kinase) and NF-kappa B activation. In addition, PAF, OxLDL, IL-1 beta activates monocytes leading to increased PAF receptor mRNA levels. These results indicate that PAF and OxLDL, in a different pattern from that of IL-1 beta, regulate MCP-1 expression via pathways that involve changes in cell redox status. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
机构:
Tokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
Tokyo Med & Dent Univ, Global Ctr Excellence Program, Int Res Ctr Mol Sci Tooth & Bone Dis, Bunkyo Ku, Tokyo 1138549, JapanTokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
Aoi, Yoko
Nakahama, Ken-ichi
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Tokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, JapanTokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
Nakahama, Ken-ichi
Morita, Ikuo
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Tokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
Tokyo Med & Dent Univ, Global Ctr Excellence Program, Int Res Ctr Mol Sci Tooth & Bone Dis, Bunkyo Ku, Tokyo 1138549, JapanTokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
Morita, Ikuo
Safronova, Olga
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Tokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
Tokyo Med & Dent Univ, Global Ctr Excellence Program, Int Res Ctr Mol Sci Tooth & Bone Dis, Bunkyo Ku, Tokyo 1138549, JapanTokyo Med & Dent Univ, Dept Cellular Physiol Chem, Bunkyo Ku, Tokyo 1138549, Japan
机构:
China Med Univ, Coll Basic Med Sci, Dept Immunol, Shenyang, Peoples R ChinaChina Med Univ, Coll Basic Med Sci, Dept Immunol, Shenyang, Peoples R China
Li, Shengjun
Wang, Wei
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang, Peoples R ChinaChina Med Univ, Coll Basic Med Sci, Dept Immunol, Shenyang, Peoples R China
Wang, Wei
Zhang, Ning
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang, Peoples R ChinaChina Med Univ, Coll Basic Med Sci, Dept Immunol, Shenyang, Peoples R China
Zhang, Ning
Ma, Tingxian
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang, Peoples R ChinaChina Med Univ, Coll Basic Med Sci, Dept Immunol, Shenyang, Peoples R China
Ma, Tingxian
Zhao, Chenghai
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China Med Univ, Coll Basic Med Sci, Dept Pathophysiol, Shenyang, Peoples R ChinaChina Med Univ, Coll Basic Med Sci, Dept Immunol, Shenyang, Peoples R China
机构:
Andong Natl Univ, Ctr Biomed Mat & Biotechnol, Sch Mat Sci & Engn, Kyungbuk 760749, South KoreaAndong Natl Univ, Ctr Biomed Mat & Biotechnol, Sch Mat Sci & Engn, Kyungbuk 760749, South Korea
Oh, Kyung-Sik
Mastro, Andrea M.
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Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USAAndong Natl Univ, Ctr Biomed Mat & Biotechnol, Sch Mat Sci & Engn, Kyungbuk 760749, South Korea
Mastro, Andrea M.
Vogler, Erwin A.
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Penn State Univ, Dept Mat Sci & Engn, University Pk, PA 16802 USAAndong Natl Univ, Ctr Biomed Mat & Biotechnol, Sch Mat Sci & Engn, Kyungbuk 760749, South Korea