Extracellular annexin II is associated with divalent cation-dependent tumor cell-endothelial cell adhesion of metastatic RAW117 large-cell lymphoma cells
Using fixed microvessel endothelial cell monolayers the molecules involved in the adhesion of liver‐preferring murine RAW117 large cell lymphoma cells to murine liver‐derived microvessel endothelial cells were identified by affinity isolation. Detergent lysates obtained from poorly (P) or highly (H1...
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Veröffentlicht in: | Journal of cellular biochemistry 1993-11, Vol.53 (3), p.265-276 |
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description | Using fixed microvessel endothelial cell monolayers the molecules involved in the adhesion of liver‐preferring murine RAW117 large cell lymphoma cells to murine liver‐derived microvessel endothelial cells were identified by affinity isolation. Detergent lysates obtained from poorly (P) or highly (H10) liver‐metastatic cells inhibited RAW117‐H10 cell adhesion to hepatic sinusoidal endothelial (HSE) cell monolayers. Allowing detergent lysates of cell surface‐labeled RAW117 cells to bind to fixed HSE cell monolayers and eluting the bound components indicated that several tumor cell surface molecules ( ∼ 70, ∼ 35, ∼ 32, ∼ 22, and ∼ 14 kDa) might be involved in RAW117 cell‐HSE cell adhesion. The ∼ 35 kDa component was cation dependent in its binding to target HSE cells. Increasing detergent concentration had no effect on binding of the ∼ 35 kDa component to HSE cell monolayers, whereas treatment with 0.5 M NaCl resulted in its selective elution from HSE cells. Incubation of the HSE cell monolayers with detergent lysates from cell surface‐labeled RAW117‐H10 cells resulted in selective depletion of the ∼ 35 kDa component, suggesting that the binding is saturable. This divalent cation‐dependent molecule is one of the major tumor cell surface components bound by several types of endothelial cells and murine hepatocytes, whereas there was poor binding of this component to unfixed or fixed human red blood cells. The purified, partially ( ∼ 40%) sequenced molecule had amino acid sequence identity with murine but not bovine annexin II, indicating that it was not bound from the bovine serum used to grow RAW117 cells. Using antibodies specific for annexin II flow cytometery indicated equivalent amounts of annexin II are expressed on RAW117 cell surfaces in the absence or presence of excess EDTA, whereas annexin I was only found in low amounts on the surfaces of RAW117 cells. Annexin II antibodies inhibited by ∼ 40–50% the adhesion of RAW117 tumor cells to live or fixed endothelial cells, and purified tumor cell surface fractions containing the ∼ 35 kDa component partially inhibited ( ∼ 35%) RAW117 cell–HSE cell adhesion. The data indicate that annexin II is expressed on the extracellular surface of RAW117 cells, and cell surface–annexin II mediates a portion of the Ca2+‐dependent RAW117 cell adhesion to liver microvessel endothelial cells. |
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Detergent lysates obtained from poorly (P) or highly (H10) liver‐metastatic cells inhibited RAW117‐H10 cell adhesion to hepatic sinusoidal endothelial (HSE) cell monolayers. Allowing detergent lysates of cell surface‐labeled RAW117 cells to bind to fixed HSE cell monolayers and eluting the bound components indicated that several tumor cell surface molecules ( ∼ 70, ∼ 35, ∼ 32, ∼ 22, and ∼ 14 kDa) might be involved in RAW117 cell‐HSE cell adhesion. The ∼ 35 kDa component was cation dependent in its binding to target HSE cells. Increasing detergent concentration had no effect on binding of the ∼ 35 kDa component to HSE cell monolayers, whereas treatment with 0.5 M NaCl resulted in its selective elution from HSE cells. Incubation of the HSE cell monolayers with detergent lysates from cell surface‐labeled RAW117‐H10 cells resulted in selective depletion of the ∼ 35 kDa component, suggesting that the binding is saturable. This divalent cation‐dependent molecule is one of the major tumor cell surface components bound by several types of endothelial cells and murine hepatocytes, whereas there was poor binding of this component to unfixed or fixed human red blood cells. The purified, partially ( ∼ 40%) sequenced molecule had amino acid sequence identity with murine but not bovine annexin II, indicating that it was not bound from the bovine serum used to grow RAW117 cells. Using antibodies specific for annexin II flow cytometery indicated equivalent amounts of annexin II are expressed on RAW117 cell surfaces in the absence or presence of excess EDTA, whereas annexin I was only found in low amounts on the surfaces of RAW117 cells. Annexin II antibodies inhibited by ∼ 40–50% the adhesion of RAW117 tumor cells to live or fixed endothelial cells, and purified tumor cell surface fractions containing the ∼ 35 kDa component partially inhibited ( ∼ 35%) RAW117 cell–HSE cell adhesion. The data indicate that annexin II is expressed on the extracellular surface of RAW117 cells, and cell surface–annexin II mediates a portion of the Ca2+‐dependent RAW117 cell adhesion to liver microvessel endothelial cells.</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.240530311</identifier><identifier>PMID: 8263043</identifier><identifier>CODEN: JCEBD5</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Amino Acid Sequence ; Animals ; Annexin A2 - chemistry ; Annexin A2 - metabolism ; Biological and medical sciences ; Calcium - pharmacology ; calpactin ; Cations, Divalent ; Cattle ; Cell Adhesion ; cell surface ; Cholic Acids ; Endothelium, Vascular - pathology ; Extracellular Space - metabolism ; Flow Cytometry ; General aspects (metabolism, cell proliferation, established cell line...) ; Humans ; lipocortin ; Liver - blood supply ; liver endothelium ; Liver Neoplasms - secondary ; Lymphoma, Large B-Cell, Diffuse - pathology ; Magnesium - pharmacology ; Medical sciences ; Mice ; Microcirculation - pathology ; Molecular Sequence Data ; Sequence Homology, Amino Acid ; Tumor cell ; tumor cell implantation ; Tumor Cells, Cultured ; tumor metastasis ; Tumors</subject><ispartof>Journal of cellular biochemistry, 1993-11, Vol.53 (3), p.265-276</ispartof><rights>Copyright © 1993 Wiley‐Liss, Inc.</rights><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4031-510f84fc8e0f26c7166c03b2aa1b71936d2f44662802bd660f4a0a4fe4a90ebc3</citedby><cites>FETCH-LOGICAL-c4031-510f84fc8e0f26c7166c03b2aa1b71936d2f44662802bd660f4a0a4fe4a90ebc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjcb.240530311$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjcb.240530311$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=3913330$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8263043$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tressler, Robert J.</creatorcontrib><creatorcontrib>Updyke, Timothy V.</creatorcontrib><creatorcontrib>Yeatman, Timothy</creatorcontrib><creatorcontrib>Nicolson, Garth L.</creatorcontrib><title>Extracellular annexin II is associated with divalent cation-dependent tumor cell-endothelial cell adhesion of metastatic RAW117 large-cell lymphoma cells</title><title>Journal of cellular biochemistry</title><addtitle>J. Cell. Biochem</addtitle><description>Using fixed microvessel endothelial cell monolayers the molecules involved in the adhesion of liver‐preferring murine RAW117 large cell lymphoma cells to murine liver‐derived microvessel endothelial cells were identified by affinity isolation. Detergent lysates obtained from poorly (P) or highly (H10) liver‐metastatic cells inhibited RAW117‐H10 cell adhesion to hepatic sinusoidal endothelial (HSE) cell monolayers. Allowing detergent lysates of cell surface‐labeled RAW117 cells to bind to fixed HSE cell monolayers and eluting the bound components indicated that several tumor cell surface molecules ( ∼ 70, ∼ 35, ∼ 32, ∼ 22, and ∼ 14 kDa) might be involved in RAW117 cell‐HSE cell adhesion. The ∼ 35 kDa component was cation dependent in its binding to target HSE cells. Increasing detergent concentration had no effect on binding of the ∼ 35 kDa component to HSE cell monolayers, whereas treatment with 0.5 M NaCl resulted in its selective elution from HSE cells. Incubation of the HSE cell monolayers with detergent lysates from cell surface‐labeled RAW117‐H10 cells resulted in selective depletion of the ∼ 35 kDa component, suggesting that the binding is saturable. This divalent cation‐dependent molecule is one of the major tumor cell surface components bound by several types of endothelial cells and murine hepatocytes, whereas there was poor binding of this component to unfixed or fixed human red blood cells. The purified, partially ( ∼ 40%) sequenced molecule had amino acid sequence identity with murine but not bovine annexin II, indicating that it was not bound from the bovine serum used to grow RAW117 cells. Using antibodies specific for annexin II flow cytometery indicated equivalent amounts of annexin II are expressed on RAW117 cell surfaces in the absence or presence of excess EDTA, whereas annexin I was only found in low amounts on the surfaces of RAW117 cells. Annexin II antibodies inhibited by ∼ 40–50% the adhesion of RAW117 tumor cells to live or fixed endothelial cells, and purified tumor cell surface fractions containing the ∼ 35 kDa component partially inhibited ( ∼ 35%) RAW117 cell–HSE cell adhesion. The data indicate that annexin II is expressed on the extracellular surface of RAW117 cells, and cell surface–annexin II mediates a portion of the Ca2+‐dependent RAW117 cell adhesion to liver microvessel endothelial cells.</description><subject>Amino Acid Sequence</subject><subject>Animals</subject><subject>Annexin A2 - chemistry</subject><subject>Annexin A2 - metabolism</subject><subject>Biological and medical sciences</subject><subject>Calcium - pharmacology</subject><subject>calpactin</subject><subject>Cations, Divalent</subject><subject>Cattle</subject><subject>Cell Adhesion</subject><subject>cell surface</subject><subject>Cholic Acids</subject><subject>Endothelium, Vascular - pathology</subject><subject>Extracellular Space - metabolism</subject><subject>Flow Cytometry</subject><subject>General aspects (metabolism, cell proliferation, established cell line...)</subject><subject>Humans</subject><subject>lipocortin</subject><subject>Liver - blood supply</subject><subject>liver endothelium</subject><subject>Liver Neoplasms - secondary</subject><subject>Lymphoma, Large B-Cell, Diffuse - pathology</subject><subject>Magnesium - pharmacology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Microcirculation - pathology</subject><subject>Molecular Sequence Data</subject><subject>Sequence Homology, Amino Acid</subject><subject>Tumor cell</subject><subject>tumor cell implantation</subject><subject>Tumor Cells, Cultured</subject><subject>tumor metastasis</subject><subject>Tumors</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1vEzEQhi0EKiFw5IjkA-K2xV_x7h7bqLRBFUh8qBUXa9ZrExfvbmo7NPkp_bd1klXEiZOlmWfe9x0PQm8pOaWEsI93ujllgsw44ZQ-QxNK6rIQUojnaEJKTgrGKXuJXsV4Rwipa85O0EnFJCeCT9DjxSYF0Mb7tYeAoe_NxvV4scAuYohx0A6SafGDS0vcur_gTZ-whuSGvmjNyvTtrpDW3RDwTqbIlSEtjXfg9wUM7dLEjOPB4s4kiClPa_zt7IbSEmfX36bYg37brZZDB_ux-Bq9sOCjeTO-U_Tz08WP-VVx_fVyMT-7LrTIGxczSmwlrK4MsUzqkkqpCW8YAG1KWnPZMiuElKwirGmlJFYAAWGNgJqYRvMp-nDQXYXhfm1iUp2LuwTQm2EdVSkp51JWGSwOoA5DjMFYtQqug7BVlKjdKVQ-hTqeIvPvRuF105n2SI9_n_vvxz5EDd4G6LWLR4zX2TcrTVF5wB6cN9v_e6rP8_N_A4yBXUxmc5yE8EfJkpczdfPlUrHvV-f17a9bRfkT5nGyXA</recordid><startdate>199311</startdate><enddate>199311</enddate><creator>Tressler, Robert J.</creator><creator>Updyke, Timothy V.</creator><creator>Yeatman, Timothy</creator><creator>Nicolson, Garth L.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>BSCLL</scope><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><scope>7X8</scope></search><sort><creationdate>199311</creationdate><title>Extracellular annexin II is associated with divalent cation-dependent tumor cell-endothelial cell adhesion of metastatic RAW117 large-cell lymphoma cells</title><author>Tressler, Robert J. ; Updyke, Timothy V. ; Yeatman, Timothy ; Nicolson, Garth L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4031-510f84fc8e0f26c7166c03b2aa1b71936d2f44662802bd660f4a0a4fe4a90ebc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Amino Acid Sequence</topic><topic>Animals</topic><topic>Annexin A2 - chemistry</topic><topic>Annexin A2 - metabolism</topic><topic>Biological and medical sciences</topic><topic>Calcium - pharmacology</topic><topic>calpactin</topic><topic>Cations, Divalent</topic><topic>Cattle</topic><topic>Cell Adhesion</topic><topic>cell surface</topic><topic>Cholic Acids</topic><topic>Endothelium, Vascular - pathology</topic><topic>Extracellular Space - metabolism</topic><topic>Flow Cytometry</topic><topic>General aspects (metabolism, cell proliferation, established cell line...)</topic><topic>Humans</topic><topic>lipocortin</topic><topic>Liver - blood supply</topic><topic>liver endothelium</topic><topic>Liver Neoplasms - secondary</topic><topic>Lymphoma, Large B-Cell, Diffuse - pathology</topic><topic>Magnesium - pharmacology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Microcirculation - pathology</topic><topic>Molecular Sequence Data</topic><topic>Sequence Homology, Amino Acid</topic><topic>Tumor cell</topic><topic>tumor cell implantation</topic><topic>Tumor Cells, Cultured</topic><topic>tumor metastasis</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tressler, Robert J.</creatorcontrib><creatorcontrib>Updyke, Timothy V.</creatorcontrib><creatorcontrib>Yeatman, Timothy</creatorcontrib><creatorcontrib>Nicolson, Garth L.</creatorcontrib><collection>Istex</collection><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><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tressler, Robert J.</au><au>Updyke, Timothy V.</au><au>Yeatman, Timothy</au><au>Nicolson, Garth L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Extracellular annexin II is associated with divalent cation-dependent tumor cell-endothelial cell adhesion of metastatic RAW117 large-cell lymphoma cells</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J. Cell. Biochem</addtitle><date>1993-11</date><risdate>1993</risdate><volume>53</volume><issue>3</issue><spage>265</spage><epage>276</epage><pages>265-276</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><coden>JCEBD5</coden><abstract>Using fixed microvessel endothelial cell monolayers the molecules involved in the adhesion of liver‐preferring murine RAW117 large cell lymphoma cells to murine liver‐derived microvessel endothelial cells were identified by affinity isolation. Detergent lysates obtained from poorly (P) or highly (H10) liver‐metastatic cells inhibited RAW117‐H10 cell adhesion to hepatic sinusoidal endothelial (HSE) cell monolayers. Allowing detergent lysates of cell surface‐labeled RAW117 cells to bind to fixed HSE cell monolayers and eluting the bound components indicated that several tumor cell surface molecules ( ∼ 70, ∼ 35, ∼ 32, ∼ 22, and ∼ 14 kDa) might be involved in RAW117 cell‐HSE cell adhesion. The ∼ 35 kDa component was cation dependent in its binding to target HSE cells. Increasing detergent concentration had no effect on binding of the ∼ 35 kDa component to HSE cell monolayers, whereas treatment with 0.5 M NaCl resulted in its selective elution from HSE cells. Incubation of the HSE cell monolayers with detergent lysates from cell surface‐labeled RAW117‐H10 cells resulted in selective depletion of the ∼ 35 kDa component, suggesting that the binding is saturable. This divalent cation‐dependent molecule is one of the major tumor cell surface components bound by several types of endothelial cells and murine hepatocytes, whereas there was poor binding of this component to unfixed or fixed human red blood cells. The purified, partially ( ∼ 40%) sequenced molecule had amino acid sequence identity with murine but not bovine annexin II, indicating that it was not bound from the bovine serum used to grow RAW117 cells. Using antibodies specific for annexin II flow cytometery indicated equivalent amounts of annexin II are expressed on RAW117 cell surfaces in the absence or presence of excess EDTA, whereas annexin I was only found in low amounts on the surfaces of RAW117 cells. Annexin II antibodies inhibited by ∼ 40–50% the adhesion of RAW117 tumor cells to live or fixed endothelial cells, and purified tumor cell surface fractions containing the ∼ 35 kDa component partially inhibited ( ∼ 35%) RAW117 cell–HSE cell adhesion. The data indicate that annexin II is expressed on the extracellular surface of RAW117 cells, and cell surface–annexin II mediates a portion of the Ca2+‐dependent RAW117 cell adhesion to liver microvessel endothelial cells.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>8263043</pmid><doi>10.1002/jcb.240530311</doi><tpages>12</tpages></addata></record> |
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subjects | Amino Acid Sequence Animals Annexin A2 - chemistry Annexin A2 - metabolism Biological and medical sciences Calcium - pharmacology calpactin Cations, Divalent Cattle Cell Adhesion cell surface Cholic Acids Endothelium, Vascular - pathology Extracellular Space - metabolism Flow Cytometry General aspects (metabolism, cell proliferation, established cell line...) Humans lipocortin Liver - blood supply liver endothelium Liver Neoplasms - secondary Lymphoma, Large B-Cell, Diffuse - pathology Magnesium - pharmacology Medical sciences Mice Microcirculation - pathology Molecular Sequence Data Sequence Homology, Amino Acid Tumor cell tumor cell implantation Tumor Cells, Cultured tumor metastasis Tumors |
title | Extracellular annexin II is associated with divalent cation-dependent tumor cell-endothelial cell adhesion of metastatic RAW117 large-cell lymphoma cells |
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