Midkine Expression in Human Periapical Granulomas
Abstract Introduction The expression of midkine (MK), a heparin-binding growth factor, is increased in various human tumors, making it a promising tumor marker and target for tumor therapy. MK is also related to the regulation of the development and etiology of chronic or autoimmune diseases; howeve...
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description | Abstract Introduction The expression of midkine (MK), a heparin-binding growth factor, is increased in various human tumors, making it a promising tumor marker and target for tumor therapy. MK is also related to the regulation of the development and etiology of chronic or autoimmune diseases; however, the involvement of MK in apical periodontitis has never been examined. This study compared the localization of MK-expressing cells and MK messenger RNA expression in periapical granulomas with healthy gingival tissues. Methods Periapical lesions were removed surgically from chronic apical periodontitis patients, and serial tissue sections were stained with hematoxylin-eosin. The lesions diagnosed as periapical granulomas pathologically were examined by immunohistochemistry using human MK monoclonal antibodies. MK messenger RNA expression was also detected using real-time polymerase chain reaction analysis. Healthy gingival tissues were analyzed in the same manner. Results MK was expressed by inflammatory cells, such as macrophages, lymphocytes, and neutrophils, as well as by endothelial cells in periapical granulomas but not in healthy gingival tissues. The MK-expressing inflammatory cells were seen adjacent to blood vessels, which contained MK-expressing endothelial cells, suggesting the interaction of MK among these cells during the process of inflammatory cell infiltration. Quantitative analysis of MK messenger RNA expression revealed that periapical granulomas expressed significantly more MK than healthy gingival tissues. Conclusions These findings suggest that MK is involved in the pathogenesis of periapical granulomas. |
doi_str_mv | 10.1016/j.joen.2011.03.009 |
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MK is also related to the regulation of the development and etiology of chronic or autoimmune diseases; however, the involvement of MK in apical periodontitis has never been examined. This study compared the localization of MK-expressing cells and MK messenger RNA expression in periapical granulomas with healthy gingival tissues. Methods Periapical lesions were removed surgically from chronic apical periodontitis patients, and serial tissue sections were stained with hematoxylin-eosin. The lesions diagnosed as periapical granulomas pathologically were examined by immunohistochemistry using human MK monoclonal antibodies. MK messenger RNA expression was also detected using real-time polymerase chain reaction analysis. Healthy gingival tissues were analyzed in the same manner. Results MK was expressed by inflammatory cells, such as macrophages, lymphocytes, and neutrophils, as well as by endothelial cells in periapical granulomas but not in healthy gingival tissues. The MK-expressing inflammatory cells were seen adjacent to blood vessels, which contained MK-expressing endothelial cells, suggesting the interaction of MK among these cells during the process of inflammatory cell infiltration. Quantitative analysis of MK messenger RNA expression revealed that periapical granulomas expressed significantly more MK than healthy gingival tissues. Conclusions These findings suggest that MK is involved in the pathogenesis of periapical granulomas.</description><identifier>ISSN: 0099-2399</identifier><identifier>EISSN: 1878-3554</identifier><identifier>DOI: 10.1016/j.joen.2011.03.009</identifier><identifier>PMID: 21787488</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antibodies, Monoclonal ; Chronic apical periodontitis ; Cytokines - analysis ; Cytokines - genetics ; Dentistry ; Endocrinology & Metabolism ; endothelial cells ; Endothelial Cells - pathology ; Endothelium, Vascular - pathology ; Female ; Gingiva - cytology ; Humans ; Immunohistochemistry ; Lymphocytes - pathology ; Macrophages - pathology ; Male ; Middle Aged ; midkine ; Nerve Growth Factors - analysis ; Nerve Growth Factors - genetics ; Neutrophils - pathology ; Periapical Granuloma - pathology ; periapical granulomas ; Real-Time Polymerase Chain Reaction ; RNA, Messenger - analysis ; Young Adult</subject><ispartof>Journal of endodontics, 2011-06, Vol.37 (6), p.781-785</ispartof><rights>American Association of Endodontists</rights><rights>2011 American Association of Endodontists</rights><rights>Copyright © 2011 American Association of Endodontists. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c410t-7651ed485b7f3784116e76bfdc6e0030e1d70213feea6d1a4f8fa64806085d13</citedby><cites>FETCH-LOGICAL-c410t-7651ed485b7f3784116e76bfdc6e0030e1d70213feea6d1a4f8fa64806085d13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0099239911003670$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21787488$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hatori, Keisuke, DDS</creatorcontrib><creatorcontrib>Takeichi, Osamu, DDS, PhD</creatorcontrib><creatorcontrib>Ogiso, Bunnai, DDS, PhD</creatorcontrib><creatorcontrib>Maeno, Masao, DDS, PhD</creatorcontrib><creatorcontrib>Komiyama, Kazuo, DDS, PhD</creatorcontrib><title>Midkine Expression in Human Periapical Granulomas</title><title>Journal of endodontics</title><addtitle>J Endod</addtitle><description>Abstract Introduction The expression of midkine (MK), a heparin-binding growth factor, is increased in various human tumors, making it a promising tumor marker and target for tumor therapy. MK is also related to the regulation of the development and etiology of chronic or autoimmune diseases; however, the involvement of MK in apical periodontitis has never been examined. This study compared the localization of MK-expressing cells and MK messenger RNA expression in periapical granulomas with healthy gingival tissues. Methods Periapical lesions were removed surgically from chronic apical periodontitis patients, and serial tissue sections were stained with hematoxylin-eosin. The lesions diagnosed as periapical granulomas pathologically were examined by immunohistochemistry using human MK monoclonal antibodies. MK messenger RNA expression was also detected using real-time polymerase chain reaction analysis. Healthy gingival tissues were analyzed in the same manner. Results MK was expressed by inflammatory cells, such as macrophages, lymphocytes, and neutrophils, as well as by endothelial cells in periapical granulomas but not in healthy gingival tissues. The MK-expressing inflammatory cells were seen adjacent to blood vessels, which contained MK-expressing endothelial cells, suggesting the interaction of MK among these cells during the process of inflammatory cell infiltration. Quantitative analysis of MK messenger RNA expression revealed that periapical granulomas expressed significantly more MK than healthy gingival tissues. Conclusions These findings suggest that MK is involved in the pathogenesis of periapical granulomas.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antibodies, Monoclonal</subject><subject>Chronic apical periodontitis</subject><subject>Cytokines - analysis</subject><subject>Cytokines - genetics</subject><subject>Dentistry</subject><subject>Endocrinology & Metabolism</subject><subject>endothelial cells</subject><subject>Endothelial Cells - pathology</subject><subject>Endothelium, Vascular - pathology</subject><subject>Female</subject><subject>Gingiva - cytology</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Lymphocytes - pathology</subject><subject>Macrophages - pathology</subject><subject>Male</subject><subject>Middle Aged</subject><subject>midkine</subject><subject>Nerve Growth Factors - analysis</subject><subject>Nerve Growth Factors - genetics</subject><subject>Neutrophils - pathology</subject><subject>Periapical Granuloma - pathology</subject><subject>periapical granulomas</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>RNA, Messenger - analysis</subject><subject>Young Adult</subject><issn>0099-2399</issn><issn>1878-3554</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcFq3DAQhkVpaTZJX6CH4ltPdmYsW5IhFEpIk0BKAsldaKUxyLHlrbQuzdtXZpMceuhpYPj-H-Ybxj4jVAgozoZqmClUNSBWwCuA7h3boJKq5G3bvGebvOnKmnfdETtOaQBAybn8yI5qlEo2Sm0Y_vTuyQcqLv_sIqXk51D4UFwvkwnFPUVvdt6asbiKJizjPJl0yj70Zkz06WWesMcfl48X1-Xt3dXNxffb0jYI-1KKFsk1qt3KnkvVIAqSYts7KwiAA6GTUCPviYxwaJpe9UY0CgSo1iE_YV8Ptbs4_1oo7fXkk6VxNIHmJWkluwy3nGeyPpA2zilF6vUu-snEZ42gV1F60KsovYrSwHXWkkNfXuqX7UTuLfJqJgPnB4Dyjb89RZ2sp2DJ-Uh2r93s_9__7Z-4HX1YVT7RM6VhXmLI9jTqVGvQD-ur1k8hZjlCAv8Lv4aNFQ</recordid><startdate>20110601</startdate><enddate>20110601</enddate><creator>Hatori, Keisuke, DDS</creator><creator>Takeichi, Osamu, DDS, PhD</creator><creator>Ogiso, Bunnai, DDS, PhD</creator><creator>Maeno, Masao, DDS, PhD</creator><creator>Komiyama, Kazuo, DDS, PhD</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20110601</creationdate><title>Midkine Expression in Human Periapical Granulomas</title><author>Hatori, Keisuke, DDS ; Takeichi, Osamu, DDS, PhD ; Ogiso, Bunnai, DDS, PhD ; Maeno, Masao, DDS, PhD ; Komiyama, Kazuo, DDS, PhD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c410t-7651ed485b7f3784116e76bfdc6e0030e1d70213feea6d1a4f8fa64806085d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antibodies, Monoclonal</topic><topic>Chronic apical periodontitis</topic><topic>Cytokines - analysis</topic><topic>Cytokines - genetics</topic><topic>Dentistry</topic><topic>Endocrinology & Metabolism</topic><topic>endothelial cells</topic><topic>Endothelial Cells - pathology</topic><topic>Endothelium, Vascular - pathology</topic><topic>Female</topic><topic>Gingiva - cytology</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Lymphocytes - pathology</topic><topic>Macrophages - pathology</topic><topic>Male</topic><topic>Middle Aged</topic><topic>midkine</topic><topic>Nerve Growth Factors - analysis</topic><topic>Nerve Growth Factors - genetics</topic><topic>Neutrophils - pathology</topic><topic>Periapical Granuloma - pathology</topic><topic>periapical granulomas</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>RNA, Messenger - analysis</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hatori, Keisuke, DDS</creatorcontrib><creatorcontrib>Takeichi, Osamu, DDS, PhD</creatorcontrib><creatorcontrib>Ogiso, Bunnai, DDS, PhD</creatorcontrib><creatorcontrib>Maeno, Masao, DDS, PhD</creatorcontrib><creatorcontrib>Komiyama, Kazuo, DDS, PhD</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of endodontics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hatori, Keisuke, DDS</au><au>Takeichi, Osamu, DDS, PhD</au><au>Ogiso, Bunnai, DDS, PhD</au><au>Maeno, Masao, DDS, PhD</au><au>Komiyama, Kazuo, DDS, PhD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Midkine Expression in Human Periapical Granulomas</atitle><jtitle>Journal of endodontics</jtitle><addtitle>J Endod</addtitle><date>2011-06-01</date><risdate>2011</risdate><volume>37</volume><issue>6</issue><spage>781</spage><epage>785</epage><pages>781-785</pages><issn>0099-2399</issn><eissn>1878-3554</eissn><abstract>Abstract Introduction The expression of midkine (MK), a heparin-binding growth factor, is increased in various human tumors, making it a promising tumor marker and target for tumor therapy. MK is also related to the regulation of the development and etiology of chronic or autoimmune diseases; however, the involvement of MK in apical periodontitis has never been examined. This study compared the localization of MK-expressing cells and MK messenger RNA expression in periapical granulomas with healthy gingival tissues. Methods Periapical lesions were removed surgically from chronic apical periodontitis patients, and serial tissue sections were stained with hematoxylin-eosin. The lesions diagnosed as periapical granulomas pathologically were examined by immunohistochemistry using human MK monoclonal antibodies. MK messenger RNA expression was also detected using real-time polymerase chain reaction analysis. Healthy gingival tissues were analyzed in the same manner. Results MK was expressed by inflammatory cells, such as macrophages, lymphocytes, and neutrophils, as well as by endothelial cells in periapical granulomas but not in healthy gingival tissues. The MK-expressing inflammatory cells were seen adjacent to blood vessels, which contained MK-expressing endothelial cells, suggesting the interaction of MK among these cells during the process of inflammatory cell infiltration. Quantitative analysis of MK messenger RNA expression revealed that periapical granulomas expressed significantly more MK than healthy gingival tissues. Conclusions These findings suggest that MK is involved in the pathogenesis of periapical granulomas.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>21787488</pmid><doi>10.1016/j.joen.2011.03.009</doi><tpages>5</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antibodies, Monoclonal Chronic apical periodontitis Cytokines - analysis Cytokines - genetics Dentistry Endocrinology & Metabolism endothelial cells Endothelial Cells - pathology Endothelium, Vascular - pathology Female Gingiva - cytology Humans Immunohistochemistry Lymphocytes - pathology Macrophages - pathology Male Middle Aged midkine Nerve Growth Factors - analysis Nerve Growth Factors - genetics Neutrophils - pathology Periapical Granuloma - pathology periapical granulomas Real-Time Polymerase Chain Reaction RNA, Messenger - analysis Young Adult |
title | Midkine Expression in Human Periapical Granulomas |
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