Differential expression of moesin in cells of hematopoietic lineage and lymphatic systems
Moesin is a member of the ERM family consisting of ezrin, radixin, and moesin. The protein is located in the plasma membrane similarly to ezrin and radixin, and is thought to regulate cellular movements and morphological changes. Using monoclonal antibody CR-22, the specificity of which against huma...
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Veröffentlicht in: | Histochemistry and cell biology 1998-07, Vol.110 (1), p.33-41 |
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creator | Masumoto, J Sagara, J Hayama, M Hidaka, E Katsuyama, T Taniguchi, S |
description | Moesin is a member of the ERM family consisting of ezrin, radixin, and moesin. The protein is located in the plasma membrane similarly to ezrin and radixin, and is thought to regulate cellular movements and morphological changes. Using monoclonal antibody CR-22, the specificity of which against human moesin was confirmed by immunoprecipitation and western blotting analysis, we immunohistochemically stained various formalin-fixed and paraffin-embedded human tissues, in particular, clots of bone marrow and lymphatic tissues, to examine moesin expression in cells of hematopoietic lineage and lymphatic systems. In the bone marrow, moesin was expressed in myeloid cells, while little staining was detected in erythroid cells. Moesin was highly expressed in both the center and the periphery of mature megakaryocytes. In the lymphatic tissues, moesin was strongly expressed by T-lymphocytes in the paracortex. In the mantle zone, the periphery of the germinal center, moesin was expressed by small lymphocytes which were identified as B-lymphocytes. Furthermore, in areas of inflammation, moesin was expressed in both the center and the periphery of neutrophils, whereas in some neutrophils in distant areas, moesin was localized at the cellular periphery. These results suggest that differential expression of moesin in these cells is involved in their morphology and specialized functions. |
doi_str_mv | 10.1007/s004180050262 |
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The protein is located in the plasma membrane similarly to ezrin and radixin, and is thought to regulate cellular movements and morphological changes. Using monoclonal antibody CR-22, the specificity of which against human moesin was confirmed by immunoprecipitation and western blotting analysis, we immunohistochemically stained various formalin-fixed and paraffin-embedded human tissues, in particular, clots of bone marrow and lymphatic tissues, to examine moesin expression in cells of hematopoietic lineage and lymphatic systems. In the bone marrow, moesin was expressed in myeloid cells, while little staining was detected in erythroid cells. Moesin was highly expressed in both the center and the periphery of mature megakaryocytes. In the lymphatic tissues, moesin was strongly expressed by T-lymphocytes in the paracortex. In the mantle zone, the periphery of the germinal center, moesin was expressed by small lymphocytes which were identified as B-lymphocytes. Furthermore, in areas of inflammation, moesin was expressed in both the center and the periphery of neutrophils, whereas in some neutrophils in distant areas, moesin was localized at the cellular periphery. These results suggest that differential expression of moesin in these cells is involved in their morphology and specialized functions.</description><identifier>ISSN: 0948-6143</identifier><identifier>EISSN: 1432-119X</identifier><identifier>DOI: 10.1007/s004180050262</identifier><identifier>PMID: 9681687</identifier><language>eng</language><publisher>Germany: Springer Nature B.V</publisher><subject>Antibodies, Monoclonal - immunology ; B-Lymphocytes - metabolism ; Blotting, Western ; Bone marrow ; Bone Marrow Cells - metabolism ; Cell Lineage ; Cytology ; Erythroid cells ; Ezrin ; Flow Cytometry ; Hematopoietic Stem Cells - metabolism ; Humans ; Immunohistochemistry ; Immunoprecipitation ; Leukocytes (neutrophilic) ; Lymphocytes ; Lymphocytes B ; Lymphocytes T ; Lymphoid Tissue - cytology ; Lymphoid Tissue - metabolism ; Megakaryocytes ; Microfilament Proteins ; Microscopy, Electron ; Moesin ; Monoclonal antibodies ; Myeloid cells ; Neutrophils ; Neutrophils - metabolism ; Paraffin ; Precipitin Tests ; Protein Biosynthesis ; Proteins - immunology ; Radixin ; T-Lymphocytes - metabolism ; Tissue Fixation ; Western blotting</subject><ispartof>Histochemistry and cell biology, 1998-07, Vol.110 (1), p.33-41</ispartof><rights>Springer-Verlag Berlin Heidelberg 1998.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c316t-3cb07daeeeb0f46c62002507e9104fe884b7703d0f9f21008fbea0dfb09372503</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9681687$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Masumoto, J</creatorcontrib><creatorcontrib>Sagara, J</creatorcontrib><creatorcontrib>Hayama, M</creatorcontrib><creatorcontrib>Hidaka, E</creatorcontrib><creatorcontrib>Katsuyama, T</creatorcontrib><creatorcontrib>Taniguchi, S</creatorcontrib><title>Differential expression of moesin in cells of hematopoietic lineage and lymphatic systems</title><title>Histochemistry and cell biology</title><addtitle>Histochem Cell Biol</addtitle><description>Moesin is a member of the ERM family consisting of ezrin, radixin, and moesin. The protein is located in the plasma membrane similarly to ezrin and radixin, and is thought to regulate cellular movements and morphological changes. Using monoclonal antibody CR-22, the specificity of which against human moesin was confirmed by immunoprecipitation and western blotting analysis, we immunohistochemically stained various formalin-fixed and paraffin-embedded human tissues, in particular, clots of bone marrow and lymphatic tissues, to examine moesin expression in cells of hematopoietic lineage and lymphatic systems. In the bone marrow, moesin was expressed in myeloid cells, while little staining was detected in erythroid cells. Moesin was highly expressed in both the center and the periphery of mature megakaryocytes. In the lymphatic tissues, moesin was strongly expressed by T-lymphocytes in the paracortex. In the mantle zone, the periphery of the germinal center, moesin was expressed by small lymphocytes which were identified as B-lymphocytes. Furthermore, in areas of inflammation, moesin was expressed in both the center and the periphery of neutrophils, whereas in some neutrophils in distant areas, moesin was localized at the cellular periphery. These results suggest that differential expression of moesin in these cells is involved in their morphology and specialized functions.</description><subject>Antibodies, Monoclonal - immunology</subject><subject>B-Lymphocytes - metabolism</subject><subject>Blotting, Western</subject><subject>Bone marrow</subject><subject>Bone Marrow Cells - metabolism</subject><subject>Cell Lineage</subject><subject>Cytology</subject><subject>Erythroid cells</subject><subject>Ezrin</subject><subject>Flow Cytometry</subject><subject>Hematopoietic Stem Cells - metabolism</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Immunoprecipitation</subject><subject>Leukocytes (neutrophilic)</subject><subject>Lymphocytes</subject><subject>Lymphocytes B</subject><subject>Lymphocytes T</subject><subject>Lymphoid Tissue - cytology</subject><subject>Lymphoid Tissue - metabolism</subject><subject>Megakaryocytes</subject><subject>Microfilament Proteins</subject><subject>Microscopy, Electron</subject><subject>Moesin</subject><subject>Monoclonal antibodies</subject><subject>Myeloid cells</subject><subject>Neutrophils</subject><subject>Neutrophils - metabolism</subject><subject>Paraffin</subject><subject>Precipitin Tests</subject><subject>Protein Biosynthesis</subject><subject>Proteins - immunology</subject><subject>Radixin</subject><subject>T-Lymphocytes - metabolism</subject><subject>Tissue Fixation</subject><subject>Western blotting</subject><issn>0948-6143</issn><issn>1432-119X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpdkN1LwzAUxYMoc04ffRQKgm_VmzRLmkeZnzDwRUGfStreuIy2qUkL7r83Y0NQOHDh8ONw7iHknMI1BZA3AYDTHGAOTLADMqU8Yyml6v2QTEHxPBXROSYnIawB6FwxNiETJXIqcjklH3fWGPTYDVY3CX73HkOwrkucSVqHwXZJVIVNE7bWCls9uN5ZHGyVNLZD_YmJ7uqk2bT9Sm_dsAkDtuGUHBndBDzb3xl5e7h_XTyly5fH58XtMq0yKoY0q0qQtUbEEgwXlWAAbA4SFQVuMM95KSVkNRhlWHw4NyVqqE0JKpMRzGbkapfbe_c1YhiK1oZtYd2hG0MRp2Eyi5qRy3_g2o2-i90KxkFypZhQkUp3VOVdCB5N0Xvbar8pKBTbwYs_g0f-Yp86li3Wv_R-4ewHwcR7DA</recordid><startdate>19980701</startdate><enddate>19980701</enddate><creator>Masumoto, J</creator><creator>Sagara, J</creator><creator>Hayama, M</creator><creator>Hidaka, E</creator><creator>Katsuyama, T</creator><creator>Taniguchi, S</creator><general>Springer Nature B.V</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>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>19980701</creationdate><title>Differential expression of moesin in cells of hematopoietic lineage and lymphatic systems</title><author>Masumoto, J ; Sagara, J ; Hayama, M ; Hidaka, E ; Katsuyama, T ; Taniguchi, S</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c316t-3cb07daeeeb0f46c62002507e9104fe884b7703d0f9f21008fbea0dfb09372503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Antibodies, Monoclonal - immunology</topic><topic>B-Lymphocytes - metabolism</topic><topic>Blotting, Western</topic><topic>Bone marrow</topic><topic>Bone Marrow Cells - metabolism</topic><topic>Cell Lineage</topic><topic>Cytology</topic><topic>Erythroid cells</topic><topic>Ezrin</topic><topic>Flow Cytometry</topic><topic>Hematopoietic Stem Cells - metabolism</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Immunoprecipitation</topic><topic>Leukocytes (neutrophilic)</topic><topic>Lymphocytes</topic><topic>Lymphocytes B</topic><topic>Lymphocytes T</topic><topic>Lymphoid Tissue - cytology</topic><topic>Lymphoid Tissue - metabolism</topic><topic>Megakaryocytes</topic><topic>Microfilament Proteins</topic><topic>Microscopy, Electron</topic><topic>Moesin</topic><topic>Monoclonal antibodies</topic><topic>Myeloid cells</topic><topic>Neutrophils</topic><topic>Neutrophils - metabolism</topic><topic>Paraffin</topic><topic>Precipitin Tests</topic><topic>Protein Biosynthesis</topic><topic>Proteins - immunology</topic><topic>Radixin</topic><topic>T-Lymphocytes - metabolism</topic><topic>Tissue Fixation</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Masumoto, J</creatorcontrib><creatorcontrib>Sagara, J</creatorcontrib><creatorcontrib>Hayama, M</creatorcontrib><creatorcontrib>Hidaka, E</creatorcontrib><creatorcontrib>Katsuyama, T</creatorcontrib><creatorcontrib>Taniguchi, S</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Histochemistry and cell biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Masumoto, J</au><au>Sagara, J</au><au>Hayama, M</au><au>Hidaka, E</au><au>Katsuyama, T</au><au>Taniguchi, S</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential expression of moesin in cells of hematopoietic lineage and lymphatic systems</atitle><jtitle>Histochemistry and cell biology</jtitle><addtitle>Histochem Cell Biol</addtitle><date>1998-07-01</date><risdate>1998</risdate><volume>110</volume><issue>1</issue><spage>33</spage><epage>41</epage><pages>33-41</pages><issn>0948-6143</issn><eissn>1432-119X</eissn><abstract>Moesin is a member of the ERM family consisting of ezrin, radixin, and moesin. The protein is located in the plasma membrane similarly to ezrin and radixin, and is thought to regulate cellular movements and morphological changes. Using monoclonal antibody CR-22, the specificity of which against human moesin was confirmed by immunoprecipitation and western blotting analysis, we immunohistochemically stained various formalin-fixed and paraffin-embedded human tissues, in particular, clots of bone marrow and lymphatic tissues, to examine moesin expression in cells of hematopoietic lineage and lymphatic systems. In the bone marrow, moesin was expressed in myeloid cells, while little staining was detected in erythroid cells. Moesin was highly expressed in both the center and the periphery of mature megakaryocytes. In the lymphatic tissues, moesin was strongly expressed by T-lymphocytes in the paracortex. In the mantle zone, the periphery of the germinal center, moesin was expressed by small lymphocytes which were identified as B-lymphocytes. Furthermore, in areas of inflammation, moesin was expressed in both the center and the periphery of neutrophils, whereas in some neutrophils in distant areas, moesin was localized at the cellular periphery. These results suggest that differential expression of moesin in these cells is involved in their morphology and specialized functions.</abstract><cop>Germany</cop><pub>Springer Nature B.V</pub><pmid>9681687</pmid><doi>10.1007/s004180050262</doi><tpages>9</tpages></addata></record> |
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subjects | Antibodies, Monoclonal - immunology B-Lymphocytes - metabolism Blotting, Western Bone marrow Bone Marrow Cells - metabolism Cell Lineage Cytology Erythroid cells Ezrin Flow Cytometry Hematopoietic Stem Cells - metabolism Humans Immunohistochemistry Immunoprecipitation Leukocytes (neutrophilic) Lymphocytes Lymphocytes B Lymphocytes T Lymphoid Tissue - cytology Lymphoid Tissue - metabolism Megakaryocytes Microfilament Proteins Microscopy, Electron Moesin Monoclonal antibodies Myeloid cells Neutrophils Neutrophils - metabolism Paraffin Precipitin Tests Protein Biosynthesis Proteins - immunology Radixin T-Lymphocytes - metabolism Tissue Fixation Western blotting |
title | Differential expression of moesin in cells of hematopoietic lineage and lymphatic systems |
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