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Antibodies to tubulin and actin bind to the surface of a human monocytic cell line, U937
Intermittent reports of cytoskeleton proteins (actin and tubulin) on the cell surface have appeared over the last 13 years. Whereas most have concentrated on lymphocytes, this study provides evidence for the presence of these proteins on the surface of a human cultured monocyte-like cell line, U937....
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Published in: | The journal of histochemistry and cytochemistry 1991-07, Vol.39 (7), p.981-985 |
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creator | Por, SB Cooley, MA Breit, SN Penny, R French, PW |
description | Intermittent reports of cytoskeleton proteins (actin and tubulin) on the cell surface have appeared over the last 13 years. Whereas most have concentrated on lymphocytes, this study provides evidence for the presence of these proteins on the surface of a human cultured monocyte-like cell line, U937. Both actin and tubulin were detected on the surface of U937 cells by flow cytometry, using an indirect staining procedure based on biotin-streptavidin-phycoerythrin, chosen for greater sensitivity. By use of this procedure, the majority of viable unstimulated U937 cells stained positively for actin and tubulin, although the level of fluorescence intensity was low. With an antibody specific for tyrosine-tubulin, most of the surface tubulin was also found to be tyrosinylated. For vimentin, an intermediate filament protein abundantly present in the cytoplasm of U937 cells, no staining could be detected. Confirmation of the flow cytometry data for surface actin and tubulin on unstimulated U937 cells was achieved by direct vesualization using a confocal laser scanning microscope. When U937 cells were activated with PMA and LPS, a marked reduction in the level of cell surface actin and tubulin occurred. The role of cell surface actin and tubulin on unstimulated U937 cells, in terms of monocyte function, remains to be elucidated. |
doi_str_mv | 10.1177/39.7.1865114 |
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Whereas most have concentrated on lymphocytes, this study provides evidence for the presence of these proteins on the surface of a human cultured monocyte-like cell line, U937. Both actin and tubulin were detected on the surface of U937 cells by flow cytometry, using an indirect staining procedure based on biotin-streptavidin-phycoerythrin, chosen for greater sensitivity. By use of this procedure, the majority of viable unstimulated U937 cells stained positively for actin and tubulin, although the level of fluorescence intensity was low. With an antibody specific for tyrosine-tubulin, most of the surface tubulin was also found to be tyrosinylated. For vimentin, an intermediate filament protein abundantly present in the cytoplasm of U937 cells, no staining could be detected. Confirmation of the flow cytometry data for surface actin and tubulin on unstimulated U937 cells was achieved by direct vesualization using a confocal laser scanning microscope. When U937 cells were activated with PMA and LPS, a marked reduction in the level of cell surface actin and tubulin occurred. The role of cell surface actin and tubulin on unstimulated U937 cells, in terms of monocyte function, remains to be elucidated.</description><identifier>ISSN: 0022-1554</identifier><identifier>EISSN: 1551-5044</identifier><identifier>DOI: 10.1177/39.7.1865114</identifier><identifier>PMID: 1865114</identifier><identifier>CODEN: JHCYAS</identifier><language>eng</language><publisher>Los Angeles, CA: Histochemical Soc</publisher><subject>Actins - analysis ; Actins - immunology ; Antibodies, Monoclonal ; Biological and medical sciences ; Cell Line ; Cell structures and functions ; Flow Cytometry ; Fundamental and applied biological sciences. Psychology ; Humans ; Immunoblotting ; Lipopolysaccharides - pharmacology ; Microscopy, Electron, Scanning ; Molecular and cellular biology ; Monocytes - chemistry ; Monocytes - physiology ; Monocytes - ultrastructure ; Tetradecanoylphorbol Acetate - pharmacology ; Tubulin - analysis ; Tubulin - immunology</subject><ispartof>The journal of histochemistry and cytochemistry, 1991-07, Vol.39 (7), p.981-985</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c379t-d46b26ee1cb2faf9f2da0242dc19f44e6bbad90117e1602c62045db83e8c02883</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=5327271$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1865114$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Por, SB</creatorcontrib><creatorcontrib>Cooley, MA</creatorcontrib><creatorcontrib>Breit, SN</creatorcontrib><creatorcontrib>Penny, R</creatorcontrib><creatorcontrib>French, PW</creatorcontrib><title>Antibodies to tubulin and actin bind to the surface of a human monocytic cell line, U937</title><title>The journal of histochemistry and cytochemistry</title><addtitle>J Histochem Cytochem</addtitle><description>Intermittent reports of cytoskeleton proteins (actin and tubulin) on the cell surface have appeared over the last 13 years. Whereas most have concentrated on lymphocytes, this study provides evidence for the presence of these proteins on the surface of a human cultured monocyte-like cell line, U937. Both actin and tubulin were detected on the surface of U937 cells by flow cytometry, using an indirect staining procedure based on biotin-streptavidin-phycoerythrin, chosen for greater sensitivity. By use of this procedure, the majority of viable unstimulated U937 cells stained positively for actin and tubulin, although the level of fluorescence intensity was low. With an antibody specific for tyrosine-tubulin, most of the surface tubulin was also found to be tyrosinylated. For vimentin, an intermediate filament protein abundantly present in the cytoplasm of U937 cells, no staining could be detected. Confirmation of the flow cytometry data for surface actin and tubulin on unstimulated U937 cells was achieved by direct vesualization using a confocal laser scanning microscope. When U937 cells were activated with PMA and LPS, a marked reduction in the level of cell surface actin and tubulin occurred. The role of cell surface actin and tubulin on unstimulated U937 cells, in terms of monocyte function, remains to be elucidated.</description><subject>Actins - analysis</subject><subject>Actins - immunology</subject><subject>Antibodies, Monoclonal</subject><subject>Biological and medical sciences</subject><subject>Cell Line</subject><subject>Cell structures and functions</subject><subject>Flow Cytometry</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Immunoblotting</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Microscopy, Electron, Scanning</subject><subject>Molecular and cellular biology</subject><subject>Monocytes - chemistry</subject><subject>Monocytes - physiology</subject><subject>Monocytes - ultrastructure</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>Tubulin - analysis</subject><subject>Tubulin - immunology</subject><issn>0022-1554</issn><issn>1551-5044</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><recordid>eNp1kElLA0EQhRtRYozevAp90IOQib3NdgzBDQJeDHhrek06zBKmZxjy7-04g548VVHvq-UVALcYLTBO0yeaL9IFzpIYY3YGpjiOcRQjxs7BFCFColBgl-DK-z1CmLE4m4DJiE_B17Jqnay1Mx62NWw72RWugqLSUKg2ZNKF9KTsDPRdY4UysLZQwF1XigqWdVWrY-sUVKYoYOg1c7jJaXoNLqwovLkZ4wxsXp4_V2_R-uP1fbVcR4qmeRtplkiSGIOVJFbY3BItEGFEK5xbxkwipdA5CkYNThBRCUEs1jKjJlOIZBmdgfkwVzW1942x_NC4UjRHjhE__YfTnKd8NBzwuwE_dLI0-g_-1e9HXXglCtuISjn_i8WUpCTFAXscMC-2hu_rrqmCyf9WPgzszm13vWsM96UoinAA5n3f_7B5huk3nB-FGw</recordid><startdate>19910701</startdate><enddate>19910701</enddate><creator>Por, SB</creator><creator>Cooley, MA</creator><creator>Breit, SN</creator><creator>Penny, R</creator><creator>French, PW</creator><general>Histochemical Soc</general><general>SAGE Publications</general><general>Histochemical Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19910701</creationdate><title>Antibodies to tubulin and actin bind to the surface of a human monocytic cell line, U937</title><author>Por, SB ; Cooley, MA ; Breit, SN ; Penny, R ; French, PW</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c379t-d46b26ee1cb2faf9f2da0242dc19f44e6bbad90117e1602c62045db83e8c02883</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Actins - analysis</topic><topic>Actins - immunology</topic><topic>Antibodies, Monoclonal</topic><topic>Biological and medical sciences</topic><topic>Cell Line</topic><topic>Cell structures and functions</topic><topic>Flow Cytometry</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Immunoblotting</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Microscopy, Electron, Scanning</topic><topic>Molecular and cellular biology</topic><topic>Monocytes - chemistry</topic><topic>Monocytes - physiology</topic><topic>Monocytes - ultrastructure</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>Tubulin - analysis</topic><topic>Tubulin - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Por, SB</creatorcontrib><creatorcontrib>Cooley, MA</creatorcontrib><creatorcontrib>Breit, SN</creatorcontrib><creatorcontrib>Penny, R</creatorcontrib><creatorcontrib>French, PW</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>The journal of histochemistry and cytochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Por, SB</au><au>Cooley, MA</au><au>Breit, SN</au><au>Penny, R</au><au>French, PW</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Antibodies to tubulin and actin bind to the surface of a human monocytic cell line, U937</atitle><jtitle>The journal of histochemistry and cytochemistry</jtitle><addtitle>J Histochem Cytochem</addtitle><date>1991-07-01</date><risdate>1991</risdate><volume>39</volume><issue>7</issue><spage>981</spage><epage>985</epage><pages>981-985</pages><issn>0022-1554</issn><eissn>1551-5044</eissn><coden>JHCYAS</coden><abstract>Intermittent reports of cytoskeleton proteins (actin and tubulin) on the cell surface have appeared over the last 13 years. Whereas most have concentrated on lymphocytes, this study provides evidence for the presence of these proteins on the surface of a human cultured monocyte-like cell line, U937. Both actin and tubulin were detected on the surface of U937 cells by flow cytometry, using an indirect staining procedure based on biotin-streptavidin-phycoerythrin, chosen for greater sensitivity. By use of this procedure, the majority of viable unstimulated U937 cells stained positively for actin and tubulin, although the level of fluorescence intensity was low. With an antibody specific for tyrosine-tubulin, most of the surface tubulin was also found to be tyrosinylated. For vimentin, an intermediate filament protein abundantly present in the cytoplasm of U937 cells, no staining could be detected. Confirmation of the flow cytometry data for surface actin and tubulin on unstimulated U937 cells was achieved by direct vesualization using a confocal laser scanning microscope. When U937 cells were activated with PMA and LPS, a marked reduction in the level of cell surface actin and tubulin occurred. The role of cell surface actin and tubulin on unstimulated U937 cells, in terms of monocyte function, remains to be elucidated.</abstract><cop>Los Angeles, CA</cop><pub>Histochemical Soc</pub><pmid>1865114</pmid><doi>10.1177/39.7.1865114</doi><tpages>5</tpages></addata></record> |
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subjects | Actins - analysis Actins - immunology Antibodies, Monoclonal Biological and medical sciences Cell Line Cell structures and functions Flow Cytometry Fundamental and applied biological sciences. Psychology Humans Immunoblotting Lipopolysaccharides - pharmacology Microscopy, Electron, Scanning Molecular and cellular biology Monocytes - chemistry Monocytes - physiology Monocytes - ultrastructure Tetradecanoylphorbol Acetate - pharmacology Tubulin - analysis Tubulin - immunology |
title | Antibodies to tubulin and actin bind to the surface of a human monocytic cell line, U937 |
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