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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of cellular biochemistry 1993-11, Vol.53 (3), p.265-276
Hauptverfasser: Tressler, Robert J., Updyke, Timothy V., Yeatman, Timothy, Nicolson, Garth L.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 276
container_issue 3
container_start_page 265
container_title Journal of cellular biochemistry
container_volume 53
creator Tressler, Robert J.
Updyke, Timothy V.
Yeatman, Timothy
Nicolson, Garth L.
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.
doi_str_mv 10.1002/jcb.240530311
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_76133668</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>76133668</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4031-510f84fc8e0f26c7166c03b2aa1b71936d2f44662802bd660f4a0a4fe4a90ebc3</originalsourceid><addsrcrecordid>eNp9kU1vEzEQhi0EKiFw5IjkA-K2xV_x7h7bqLRBFUh8qBUXa9ZrExfvbmo7NPkp_bd1klXEiZOlmWfe9x0PQm8pOaWEsI93ujllgsw44ZQ-QxNK6rIQUojnaEJKTgrGKXuJXsV4Rwipa85O0EnFJCeCT9DjxSYF0Mb7tYeAoe_NxvV4scAuYohx0A6SafGDS0vcur_gTZ-whuSGvmjNyvTtrpDW3RDwTqbIlSEtjXfg9wUM7dLEjOPB4s4kiClPa_zt7IbSEmfX36bYg37brZZDB_ux-Bq9sOCjeTO-U_Tz08WP-VVx_fVyMT-7LrTIGxczSmwlrK4MsUzqkkqpCW8YAG1KWnPZMiuElKwirGmlJFYAAWGNgJqYRvMp-nDQXYXhfm1iUp2LuwTQm2EdVSkp51JWGSwOoA5DjMFYtQqug7BVlKjdKVQ-hTqeIvPvRuF105n2SI9_n_vvxz5EDd4G6LWLR4zX2TcrTVF5wB6cN9v_e6rP8_N_A4yBXUxmc5yE8EfJkpczdfPlUrHvV-f17a9bRfkT5nGyXA</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>76133668</pqid></control><display><type>article</type><title>Extracellular annexin II is associated with divalent cation-dependent tumor cell-endothelial cell adhesion of metastatic RAW117 large-cell lymphoma cells</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><creator>Tressler, Robert J. ; Updyke, Timothy V. ; Yeatman, Timothy ; Nicolson, Garth L.</creator><creatorcontrib>Tressler, Robert J. ; Updyke, Timothy V. ; Yeatman, Timothy ; Nicolson, Garth L.</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0730-2312
ispartof Journal of cellular biochemistry, 1993-11, Vol.53 (3), p.265-276
issn 0730-2312
1097-4644
language eng
recordid cdi_proquest_miscellaneous_76133668
source MEDLINE; Wiley Online Library Journals Frontfile Complete
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
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-21T12%3A37%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Extracellular%20annexin%20II%20is%20associated%20with%20divalent%20cation-dependent%20tumor%20cell-endothelial%20cell%20adhesion%20of%20metastatic%20RAW117%20large-cell%20lymphoma%20cells&rft.jtitle=Journal%20of%20cellular%20biochemistry&rft.au=Tressler,%20Robert%20J.&rft.date=1993-11&rft.volume=53&rft.issue=3&rft.spage=265&rft.epage=276&rft.pages=265-276&rft.issn=0730-2312&rft.eissn=1097-4644&rft.coden=JCEBD5&rft_id=info:doi/10.1002/jcb.240530311&rft_dat=%3Cproquest_cross%3E76133668%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=76133668&rft_id=info:pmid/8263043&rfr_iscdi=true