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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Veröffentlicht in:Journal of endodontics 2011-06, Vol.37 (6), p.781-785
Hauptverfasser: Hatori, Keisuke, DDS, Takeichi, Osamu, DDS, PhD, Ogiso, Bunnai, DDS, PhD, Maeno, Masao, DDS, PhD, Komiyama, Kazuo, DDS, PhD
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container_end_page 785
container_issue 6
container_start_page 781
container_title Journal of endodontics
container_volume 37
creator Hatori, Keisuke, DDS
Takeichi, Osamu, DDS, PhD
Ogiso, Bunnai, DDS, PhD
Maeno, Masao, DDS, PhD
Komiyama, Kazuo, DDS, PhD
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 &amp; 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 &amp; 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 &amp; 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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