Whole-Blood Flow-Cytometric Analysis of Induction of Adhesion Molecules Expression on Eosinophils Stimulated by Phorbol-12-Myristate-13-Acetate/Ionomycin
Background: Activation of eosinophils is closely associated with the pathology of allergic inflammatory disease, especially bronchial asthma. We recently investigated the activation of eosinophils by applying whole blood to a flow cytometer. We measured here β 1 and β 2 integrin on eosinophils stimu...
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Veröffentlicht in: | International archives of allergy and immunology 1999-01, Vol.120 (Suppl 1), p.27-29 |
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creator | Saito, Norihiro Kayaba, Hiroyuki Honda, Kohei Yamada, Yoshiyuki Cui, Chang-Hao Kamada, Yumiko Kuwasaki, Tomoe Oyamada, Hajime Chihara, Junichi |
description | Background: Activation of eosinophils is closely associated with the pathology of allergic inflammatory disease, especially bronchial asthma. We recently investigated the activation of eosinophils by applying whole blood to a flow cytometer. We measured here β 1 and β 2 integrin on eosinophils stimulated by phorbol-12-myristate-13-acetate (PMA)/ionomycin to evaluate eosinophil activation in vitro using whole blood. Methods: Heparinized whole blood was diluted with the same volume of RPMI 1640, then cells were incubated in the presence or absence of PMA and ionomycin for 45 min at 37°C. After hemolyzation with lysing solution, flow-cytometric findings for CR3, LFA1-α, LFA1-β and VLA-4 expression on eosinophils were examined. Results: Mean fluorescent intensity (MFI) of CR3 and LFA1-β stimulated by PMA and ionomycin was significantly higher than that of the unstimulated control. MFI of LFA1-α showed no significant difference from the unstimulated control. On the other hand, MFI of VLA-4 tended to decrease. Conclusions: Our method to distinguish eosinophils from various cell groups in whole blood is simple and time-saving, similar to conditions in vivo and may allow intensive investigation of eosinophils in clinical laboratories as well as in research laboratories. We are currently investigating the influence of different kinds of stimulations, regulation factors or agents on eosinophils using this method. |
doi_str_mv | 10.1159/000053589 |
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We recently investigated the activation of eosinophils by applying whole blood to a flow cytometer. We measured here β 1 and β 2 integrin on eosinophils stimulated by phorbol-12-myristate-13-acetate (PMA)/ionomycin to evaluate eosinophil activation in vitro using whole blood. Methods: Heparinized whole blood was diluted with the same volume of RPMI 1640, then cells were incubated in the presence or absence of PMA and ionomycin for 45 min at 37°C. After hemolyzation with lysing solution, flow-cytometric findings for CR3, LFA1-α, LFA1-β and VLA-4 expression on eosinophils were examined. Results: Mean fluorescent intensity (MFI) of CR3 and LFA1-β stimulated by PMA and ionomycin was significantly higher than that of the unstimulated control. MFI of LFA1-α showed no significant difference from the unstimulated control. On the other hand, MFI of VLA-4 tended to decrease. Conclusions: Our method to distinguish eosinophils from various cell groups in whole blood is simple and time-saving, similar to conditions in vivo and may allow intensive investigation of eosinophils in clinical laboratories as well as in research laboratories. We are currently investigating the influence of different kinds of stimulations, regulation factors or agents on eosinophils using this method.</description><identifier>ISSN: 1018-2438</identifier><identifier>ISBN: 3805569920</identifier><identifier>ISBN: 9783805569927</identifier><identifier>EISSN: 1423-0097</identifier><identifier>EISBN: 9783318005257</identifier><identifier>EISBN: 3318005258</identifier><identifier>DOI: 10.1159/000053589</identifier><identifier>PMID: 10529599</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Allergic diseases ; Biological and medical sciences ; Carcinogens - pharmacology ; Cell Adhesion Molecules - biosynthesis ; Eosinophils - metabolism ; Flow Cytometry ; General aspects ; Humans ; Immunopathology ; Medical sciences ; phorbol 12-myristate 13-acetate ; Tetradecanoylphorbol Acetate - pharmacology</subject><ispartof>International archives of allergy and immunology, 1999-01, Vol.120 (Suppl 1), p.27-29</ispartof><rights>1999 S. Karger AG, Basel</rights><rights>1999 INIST-CNRS</rights><rights>Copyright (c) 1999 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-dc3682de7ef4b2086fcb9217e97c74939e5ef8aa8169b05abf483364514dbb8f3</citedby><cites>FETCH-LOGICAL-c481t-dc3682de7ef4b2086fcb9217e97c74939e5ef8aa8169b05abf483364514dbb8f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>310,311,315,781,785,790,791,2430,4025,4051,4052,23935,23936,25145,27928,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=1996927$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10529599$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Saito, Norihiro</creatorcontrib><creatorcontrib>Kayaba, Hiroyuki</creatorcontrib><creatorcontrib>Honda, Kohei</creatorcontrib><creatorcontrib>Yamada, Yoshiyuki</creatorcontrib><creatorcontrib>Cui, Chang-Hao</creatorcontrib><creatorcontrib>Kamada, Yumiko</creatorcontrib><creatorcontrib>Kuwasaki, Tomoe</creatorcontrib><creatorcontrib>Oyamada, Hajime</creatorcontrib><creatorcontrib>Chihara, Junichi</creatorcontrib><title>Whole-Blood Flow-Cytometric Analysis of Induction of Adhesion Molecules Expression on Eosinophils Stimulated by Phorbol-12-Myristate-13-Acetate/Ionomycin</title><title>International archives of allergy and immunology</title><addtitle>Int Arch Allergy Immunol</addtitle><description>Background: Activation of eosinophils is closely associated with the pathology of allergic inflammatory disease, especially bronchial asthma. We recently investigated the activation of eosinophils by applying whole blood to a flow cytometer. We measured here β 1 and β 2 integrin on eosinophils stimulated by phorbol-12-myristate-13-acetate (PMA)/ionomycin to evaluate eosinophil activation in vitro using whole blood. Methods: Heparinized whole blood was diluted with the same volume of RPMI 1640, then cells were incubated in the presence or absence of PMA and ionomycin for 45 min at 37°C. After hemolyzation with lysing solution, flow-cytometric findings for CR3, LFA1-α, LFA1-β and VLA-4 expression on eosinophils were examined. Results: Mean fluorescent intensity (MFI) of CR3 and LFA1-β stimulated by PMA and ionomycin was significantly higher than that of the unstimulated control. MFI of LFA1-α showed no significant difference from the unstimulated control. On the other hand, MFI of VLA-4 tended to decrease. Conclusions: Our method to distinguish eosinophils from various cell groups in whole blood is simple and time-saving, similar to conditions in vivo and may allow intensive investigation of eosinophils in clinical laboratories as well as in research laboratories. We are currently investigating the influence of different kinds of stimulations, regulation factors or agents on eosinophils using this method.</description><subject>Allergic diseases</subject><subject>Biological and medical sciences</subject><subject>Carcinogens - pharmacology</subject><subject>Cell Adhesion Molecules - biosynthesis</subject><subject>Eosinophils - metabolism</subject><subject>Flow Cytometry</subject><subject>General aspects</subject><subject>Humans</subject><subject>Immunopathology</subject><subject>Medical sciences</subject><subject>phorbol 12-myristate 13-acetate</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><issn>1018-2438</issn><issn>1423-0097</issn><isbn>3805569920</isbn><isbn>9783805569927</isbn><isbn>9783318005257</isbn><isbn>3318005258</isbn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNptkV1rFDEUhuMX9sNeeC2UoYjgRWw-JpPkcrpsdaFFQcXLIZNJ3NTMZE1msPNT_Ldmu2sVMQRyct7nvAfOAeA5Rm8wZvIc5cMoE_IBOJFcUIpFThDGH4JDXBIKEZL8ETiiAjFWSUnQ4ywgLCApqTgARyndIJSdRPUUHOBcKpmUh-Dnl3XwBl74ELri0ocfcDGPoTdjdLqoB-Xn5FIRbLEaukmPLgzbT92tTdrG17lYT96kYnm7iSbdJfNdhuSGsFk7n4qPo-snr0bTFe1cfFiH2AYPMYHXc3RpzALEFNbabMPzVRhCP2s3PANPrPLJnOzfY_D5cvlp8Q5evX-7WtRXUJcCj7DTtBKkM9zYsiVIVFa3kmBuJNe8lFQaZqxQSuBKtoip1pZ5elXJcNm1rbD0GLza-W5i-D6ZNDa9S9p4rwYTptRgXmJCCM3g2T_gTZhiHlFqCMEiT5STDL3eQTqGlKKxzSa6XsW5wajZbrK532RmT_eGU9ub7i9yt50MvNwDKmnlbVSDdukPJ2UlCc_Yix32TcWvJt7rv7uc_Vdd1fUd0Gw6S38BrNa2Vg</recordid><startdate>199901</startdate><enddate>199901</enddate><creator>Saito, Norihiro</creator><creator>Kayaba, Hiroyuki</creator><creator>Honda, Kohei</creator><creator>Yamada, Yoshiyuki</creator><creator>Cui, Chang-Hao</creator><creator>Kamada, Yumiko</creator><creator>Kuwasaki, Tomoe</creator><creator>Oyamada, Hajime</creator><creator>Chihara, Junichi</creator><general>Karger</general><general>S. 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We recently investigated the activation of eosinophils by applying whole blood to a flow cytometer. We measured here β 1 and β 2 integrin on eosinophils stimulated by phorbol-12-myristate-13-acetate (PMA)/ionomycin to evaluate eosinophil activation in vitro using whole blood. Methods: Heparinized whole blood was diluted with the same volume of RPMI 1640, then cells were incubated in the presence or absence of PMA and ionomycin for 45 min at 37°C. After hemolyzation with lysing solution, flow-cytometric findings for CR3, LFA1-α, LFA1-β and VLA-4 expression on eosinophils were examined. Results: Mean fluorescent intensity (MFI) of CR3 and LFA1-β stimulated by PMA and ionomycin was significantly higher than that of the unstimulated control. MFI of LFA1-α showed no significant difference from the unstimulated control. On the other hand, MFI of VLA-4 tended to decrease. Conclusions: Our method to distinguish eosinophils from various cell groups in whole blood is simple and time-saving, similar to conditions in vivo and may allow intensive investigation of eosinophils in clinical laboratories as well as in research laboratories. We are currently investigating the influence of different kinds of stimulations, regulation factors or agents on eosinophils using this method.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>10529599</pmid><doi>10.1159/000053589</doi><tpages>3</tpages></addata></record> |
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subjects | Allergic diseases Biological and medical sciences Carcinogens - pharmacology Cell Adhesion Molecules - biosynthesis Eosinophils - metabolism Flow Cytometry General aspects Humans Immunopathology Medical sciences phorbol 12-myristate 13-acetate Tetradecanoylphorbol Acetate - pharmacology |
title | Whole-Blood Flow-Cytometric Analysis of Induction of Adhesion Molecules Expression on Eosinophils Stimulated by Phorbol-12-Myristate-13-Acetate/Ionomycin |
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