The presence of ferric and ferrous iron in the nonheme iron store of resident macrophages in different tissues and organs: histochemical demonstrations by the perfusion-Perls and -Turnbull methods in the rat
We previously developed the highly sensitive perfusion-Perls and -Turnbull methods to visualize nonheme ferric (Fe (III)) and ferrous (Fe (II)) iron, respectively. The present study used these methods to investigate the possible presence of nonheme iron in the redox (ferric/ferrous) state in the non...
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Veröffentlicht in: | Archives of Histology and Cytology 2005, Vol.68(3), pp.171-183 |
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creator | Meguro, Reiko Asano, Yoshiya Odagiri, Saori Li, Chengtai Iwatsuki, Hiroyasu Shoumura, Kazuhiko |
description | We previously developed the highly sensitive perfusion-Perls and -Turnbull methods to visualize nonheme ferric (Fe (III)) and ferrous (Fe (II)) iron, respectively. The present study used these methods to investigate the possible presence of nonheme iron in the redox (ferric/ferrous) state in the noneheme iron store (phagolysosomes and siderosomes) of resident macrophages in the rat. The perfusion-Perls and -Turnbull methods at pH 0.6 supplemented by DAB intensification intensely stained resident macrophages of different tissues and organs of normal and iron-overloaded rats. The perfusion-Turnbull method, which is specific for nonheme Fe (II), partly stained hemosiderin at pH 5.3, but hardly stained it at the physiological pH, suggesting the presence of some iron in the reduced form, free Fe2+ and/or loosely bound Fe (II), at the intravacuolar pH (5.4+/-0.2) of the phagolysosomes of macrophages. Electron microscopy of the splenic and hepatic macrophages treated by the perfusion-Perls or -Turnbull method showed that Fe (II) deposits were largely distributed along the margin of hemosiderin masses while Fe (III) deposits could also be found within hemosiderin masses. |
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The present study used these methods to investigate the possible presence of nonheme iron in the redox (ferric/ferrous) state in the noneheme iron store (phagolysosomes and siderosomes) of resident macrophages in the rat. The perfusion-Perls and -Turnbull methods at pH 0.6 supplemented by DAB intensification intensely stained resident macrophages of different tissues and organs of normal and iron-overloaded rats. The perfusion-Turnbull method, which is specific for nonheme Fe (II), partly stained hemosiderin at pH 5.3, but hardly stained it at the physiological pH, suggesting the presence of some iron in the reduced form, free Fe2+ and/or loosely bound Fe (II), at the intravacuolar pH (5.4+/-0.2) of the phagolysosomes of macrophages. Electron microscopy of the splenic and hepatic macrophages treated by the perfusion-Perls or -Turnbull method showed that Fe (II) deposits were largely distributed along the margin of hemosiderin masses while Fe (III) deposits could also be found within hemosiderin masses.</description><identifier>ISSN: 0914-9465</identifier><identifier>EISSN: 1349-1717</identifier><identifier>DOI: 10.1679/aohc.68.171</identifier><identifier>PMID: 16276023</identifier><language>eng</language><publisher>Japan: International Society of Histology and Cytology</publisher><subject>3,3'-Diaminobenzidine - chemistry ; 3,3'-Diaminobenzidine - metabolism ; Animals ; Female ; Ferric Compounds - metabolism ; Ferrous Compounds - analysis ; Ferrous Compounds - metabolism ; Histocytochemistry - methods ; Hydrogen-Ion Concentration ; Iron - metabolism ; Iron Chelating Agents - metabolism ; Iron Chelating Agents - pharmacology ; Iron Overload ; Kupffer Cells - metabolism ; Liver - cytology ; Liver - metabolism ; Macrophages - chemistry ; Macrophages - cytology ; Macrophages - metabolism ; Oxidation-Reduction ; Perfusion - methods ; Phagosomes ; Rats ; Rats, Wistar ; Silver Nitrate - chemistry ; Silver Nitrate - metabolism ; Spleen - cytology ; Spleen - metabolism</subject><ispartof>Archives of Histology and Cytology, 2005, Vol.68(3), pp.171-183</ispartof><rights>2005 by International Society of Histology and Cytology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c572t-420e677f768f16f768fecc5c143b2538e9cf53a70566064db8ad914a6d392fbb3</citedby><cites>FETCH-LOGICAL-c572t-420e677f768f16f768fecc5c143b2538e9cf53a70566064db8ad914a6d392fbb3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,1877,4010,27900,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16276023$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Meguro, Reiko</creatorcontrib><creatorcontrib>Asano, Yoshiya</creatorcontrib><creatorcontrib>Odagiri, Saori</creatorcontrib><creatorcontrib>Li, Chengtai</creatorcontrib><creatorcontrib>Iwatsuki, Hiroyasu</creatorcontrib><creatorcontrib>Shoumura, Kazuhiko</creatorcontrib><title>The presence of ferric and ferrous iron in the nonheme iron store of resident macrophages in different tissues and organs: histochemical demonstrations by the perfusion-Perls and -Turnbull methods in the rat</title><title>Archives of Histology and Cytology</title><addtitle>Arch. Histol. Cytol.</addtitle><description>We previously developed the highly sensitive perfusion-Perls and -Turnbull methods to visualize nonheme ferric (Fe (III)) and ferrous (Fe (II)) iron, respectively. The present study used these methods to investigate the possible presence of nonheme iron in the redox (ferric/ferrous) state in the noneheme iron store (phagolysosomes and siderosomes) of resident macrophages in the rat. The perfusion-Perls and -Turnbull methods at pH 0.6 supplemented by DAB intensification intensely stained resident macrophages of different tissues and organs of normal and iron-overloaded rats. The perfusion-Turnbull method, which is specific for nonheme Fe (II), partly stained hemosiderin at pH 5.3, but hardly stained it at the physiological pH, suggesting the presence of some iron in the reduced form, free Fe2+ and/or loosely bound Fe (II), at the intravacuolar pH (5.4+/-0.2) of the phagolysosomes of macrophages. Electron microscopy of the splenic and hepatic macrophages treated by the perfusion-Perls or -Turnbull method showed that Fe (II) deposits were largely distributed along the margin of hemosiderin masses while Fe (III) deposits could also be found within hemosiderin masses.</description><subject>3,3'-Diaminobenzidine - chemistry</subject><subject>3,3'-Diaminobenzidine - metabolism</subject><subject>Animals</subject><subject>Female</subject><subject>Ferric Compounds - metabolism</subject><subject>Ferrous Compounds - analysis</subject><subject>Ferrous Compounds - metabolism</subject><subject>Histocytochemistry - methods</subject><subject>Hydrogen-Ion Concentration</subject><subject>Iron - metabolism</subject><subject>Iron Chelating Agents - metabolism</subject><subject>Iron Chelating Agents - pharmacology</subject><subject>Iron Overload</subject><subject>Kupffer Cells - metabolism</subject><subject>Liver - cytology</subject><subject>Liver - metabolism</subject><subject>Macrophages - chemistry</subject><subject>Macrophages - cytology</subject><subject>Macrophages - metabolism</subject><subject>Oxidation-Reduction</subject><subject>Perfusion - methods</subject><subject>Phagosomes</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Silver Nitrate - chemistry</subject><subject>Silver Nitrate - metabolism</subject><subject>Spleen - cytology</subject><subject>Spleen - metabolism</subject><issn>0914-9465</issn><issn>1349-1717</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkcFu1DAQhi0EokvhxB35xKXKEseJnXACVaUgVaKH7TlynHHjKrGD7Rz6lLwSk82yvXhGM9__254h5CPL90zI5ovyg96Les8ke0V2jJdNhql8TXZ5w8qsKUV1Qd7F-JTnvOAFe0sumCikyAu-I38PA9A5QASngXpDDYRgNVWuP6Z-idQG76h1NCHqvBtggq0Wkw9HEeptDy7RSeng50E9QlwVvTVosjaSjXHB4urrw6Ny8SsdLBpotLNajbSHybuYgkoWI-2ej_fNEMwSsZLdQxg3fXZYguuWcaQTpMH38f_jUPuevDFqjPDhFC_Jw4-bw_XP7O737a_r73eZrmSRsrLIQUhppKgNE8cAWlealbwrKl5Do03FlcwrIXJR9l2tehymEj1vCtN1_JJ83nzn4P_gx1I72ahhHJUDnFkrainrStYIXm0gDibGAKadg51UeG5Z3q77a9f9Id_i0pD-dLJdugn6F_a0MAS-bcBTTDjlM6BCsnqEsxnfDvQ8t_SgQguO_wMwlbOE</recordid><startdate>2005</startdate><enddate>2005</enddate><creator>Meguro, Reiko</creator><creator>Asano, Yoshiya</creator><creator>Odagiri, Saori</creator><creator>Li, Chengtai</creator><creator>Iwatsuki, Hiroyasu</creator><creator>Shoumura, Kazuhiko</creator><general>International Society of Histology and Cytology</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>2005</creationdate><title>The presence of ferric and ferrous iron in the nonheme iron store of resident macrophages in different tissues and organs: histochemical demonstrations by the perfusion-Perls and -Turnbull methods in the rat</title><author>Meguro, Reiko ; Asano, Yoshiya ; Odagiri, Saori ; Li, Chengtai ; Iwatsuki, Hiroyasu ; Shoumura, Kazuhiko</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c572t-420e677f768f16f768fecc5c143b2538e9cf53a70566064db8ad914a6d392fbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>3,3'-Diaminobenzidine - chemistry</topic><topic>3,3'-Diaminobenzidine - metabolism</topic><topic>Animals</topic><topic>Female</topic><topic>Ferric Compounds - metabolism</topic><topic>Ferrous Compounds - analysis</topic><topic>Ferrous Compounds - metabolism</topic><topic>Histocytochemistry - methods</topic><topic>Hydrogen-Ion Concentration</topic><topic>Iron - metabolism</topic><topic>Iron Chelating Agents - metabolism</topic><topic>Iron Chelating Agents - pharmacology</topic><topic>Iron Overload</topic><topic>Kupffer Cells - metabolism</topic><topic>Liver - cytology</topic><topic>Liver - metabolism</topic><topic>Macrophages - chemistry</topic><topic>Macrophages - cytology</topic><topic>Macrophages - metabolism</topic><topic>Oxidation-Reduction</topic><topic>Perfusion - methods</topic><topic>Phagosomes</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Silver Nitrate - chemistry</topic><topic>Silver Nitrate - metabolism</topic><topic>Spleen - cytology</topic><topic>Spleen - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Meguro, Reiko</creatorcontrib><creatorcontrib>Asano, Yoshiya</creatorcontrib><creatorcontrib>Odagiri, Saori</creatorcontrib><creatorcontrib>Li, Chengtai</creatorcontrib><creatorcontrib>Iwatsuki, Hiroyasu</creatorcontrib><creatorcontrib>Shoumura, Kazuhiko</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>Archives of Histology and Cytology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Meguro, Reiko</au><au>Asano, Yoshiya</au><au>Odagiri, Saori</au><au>Li, Chengtai</au><au>Iwatsuki, Hiroyasu</au><au>Shoumura, Kazuhiko</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The presence of ferric and ferrous iron in the nonheme iron store of resident macrophages in different tissues and organs: histochemical demonstrations by the perfusion-Perls and -Turnbull methods in the rat</atitle><jtitle>Archives of Histology and Cytology</jtitle><addtitle>Arch. Histol. Cytol.</addtitle><date>2005</date><risdate>2005</risdate><volume>68</volume><issue>3</issue><spage>171</spage><epage>183</epage><pages>171-183</pages><issn>0914-9465</issn><eissn>1349-1717</eissn><abstract>We previously developed the highly sensitive perfusion-Perls and -Turnbull methods to visualize nonheme ferric (Fe (III)) and ferrous (Fe (II)) iron, respectively. The present study used these methods to investigate the possible presence of nonheme iron in the redox (ferric/ferrous) state in the noneheme iron store (phagolysosomes and siderosomes) of resident macrophages in the rat. The perfusion-Perls and -Turnbull methods at pH 0.6 supplemented by DAB intensification intensely stained resident macrophages of different tissues and organs of normal and iron-overloaded rats. The perfusion-Turnbull method, which is specific for nonheme Fe (II), partly stained hemosiderin at pH 5.3, but hardly stained it at the physiological pH, suggesting the presence of some iron in the reduced form, free Fe2+ and/or loosely bound Fe (II), at the intravacuolar pH (5.4+/-0.2) of the phagolysosomes of macrophages. Electron microscopy of the splenic and hepatic macrophages treated by the perfusion-Perls or -Turnbull method showed that Fe (II) deposits were largely distributed along the margin of hemosiderin masses while Fe (III) deposits could also be found within hemosiderin masses.</abstract><cop>Japan</cop><pub>International Society of Histology and Cytology</pub><pmid>16276023</pmid><doi>10.1679/aohc.68.171</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3,3'-Diaminobenzidine - chemistry 3,3'-Diaminobenzidine - metabolism Animals Female Ferric Compounds - metabolism Ferrous Compounds - analysis Ferrous Compounds - metabolism Histocytochemistry - methods Hydrogen-Ion Concentration Iron - metabolism Iron Chelating Agents - metabolism Iron Chelating Agents - pharmacology Iron Overload Kupffer Cells - metabolism Liver - cytology Liver - metabolism Macrophages - chemistry Macrophages - cytology Macrophages - metabolism Oxidation-Reduction Perfusion - methods Phagosomes Rats Rats, Wistar Silver Nitrate - chemistry Silver Nitrate - metabolism Spleen - cytology Spleen - metabolism |
title | The presence of ferric and ferrous iron in the nonheme iron store of resident macrophages in different tissues and organs: histochemical demonstrations by the perfusion-Perls and -Turnbull methods in the rat |
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