Soluble ICAM-1 and VCAM-1 as Markers of Endothelial Activation

Activated endothelium releases the soluble adhesion molecules vascular cell adhesion molecule-1 (sVCAM-1) and intercellular adhesion molecule-1 (sICAM-1). Measurement of fluid-phase adhesion molecules is therefore used to quantify endothelial activation, but it is unclear which is the better marker....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Scandinavian journal of immunology 2008-05, Vol.67 (5), p.523-531
Hauptverfasser: Videm, V, Albrigtsen, M
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 531
container_issue 5
container_start_page 523
container_title Scandinavian journal of immunology
container_volume 67
creator Videm, V
Albrigtsen, M
description Activated endothelium releases the soluble adhesion molecules vascular cell adhesion molecule-1 (sVCAM-1) and intercellular adhesion molecule-1 (sICAM-1). Measurement of fluid-phase adhesion molecules is therefore used to quantify endothelial activation, but it is unclear which is the better marker. The aims of the study were to compare the relationships between mRNA, surface and total expression and released VCAM-1 and ICAM-1 in endothelial cell cultures during activation, and to compare human umbilical vein endothelial cells (HUVEC) with the microvascular cell line HMEC-1. sVCAM-1 better represented mRNA and surface expression changes in HUVEC undergoing endotoxin stimulation than did sICAM-1. Very little VCAM-1 was released from endotoxin-stimulated HMEC-1, and sICAM-1 seemed a better activation marker for these cells. During incubation of HUVEC in media with glucose concentrations of 5.6, 10.6 or 20.6 m m, VCAM-1 was released to the media in a dose-dependent way without changes in surface expression. ICAM-1 was not influenced by the glucose concentration. There are situations when VCAM-1 concentrations in the media do not mirror the surface expression on HUVEC in culture, indicating that measurements of soluble adhesion molecules may not necessarily be representative of the conditions on the cell surface. Endothelium from different locations showed varying responses with respect to VCAM-1 and ICAM-1 liberation upon endotoxin stimulation. Thus, both sVCAM-1 and sICAM-1 should be quantified in clinical studies of endothelial activation until their characteristics are better clarified.
doi_str_mv 10.1111/j.1365-3083.2008.02029.x
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_70499299</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>20697158</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4729-30edb88242c60e1e462df1d5b00d32c8281df4dbf5a627f20a6f5dd995dc48f83</originalsourceid><addsrcrecordid>eNqNkUFPwyAYhonRuDn9C9qTt9YPKC0cNFmWqTNbPMx5JbSAdnbrLK1u_97WLnpULnwJz_tCHhDyMAS4WVfLANOI-RQ4DQgAD4AAEcH2APV_Dg5RHyiAL8KY9dCJc0sATElMj1EPcxpRJlgf3cyLvE5y401Gw5mPPbXW3vN-dN5MlW-mdF5hvfFaF9WryTOVe8O0yj5UlRXrU3RkVe7M2X4foMXt-Gl0708f75rGqZ-GMRHNe4xOOCchSSMw2IQR0RZrlgBoSlJOONY21IllKiKxJaAiy7QWguk05JbTAbrsejdl8V4bV8lV5lKT52ptitrJGEIhiBB_ggQiEWPWNvIOTMvCudJYuSmzlSp3EoNsJculbF3K1qVsJctvyXLbRM_3d9TJyujf4N5qA1x3wGeWm92_i-X8YdJOTf6iy1tVSPVSZk4u5qT5vQbmFEJGvwD5EZD0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>20697158</pqid></control><display><type>article</type><title>Soluble ICAM-1 and VCAM-1 as Markers of Endothelial Activation</title><source>MEDLINE</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Access via Wiley Online Library</source><source>IngentaConnect Free/Open Access Journals</source><source>Wiley Online Library (Open Access Collection)</source><creator>Videm, V ; Albrigtsen, M</creator><creatorcontrib>Videm, V ; Albrigtsen, M</creatorcontrib><description>Activated endothelium releases the soluble adhesion molecules vascular cell adhesion molecule-1 (sVCAM-1) and intercellular adhesion molecule-1 (sICAM-1). Measurement of fluid-phase adhesion molecules is therefore used to quantify endothelial activation, but it is unclear which is the better marker. The aims of the study were to compare the relationships between mRNA, surface and total expression and released VCAM-1 and ICAM-1 in endothelial cell cultures during activation, and to compare human umbilical vein endothelial cells (HUVEC) with the microvascular cell line HMEC-1. sVCAM-1 better represented mRNA and surface expression changes in HUVEC undergoing endotoxin stimulation than did sICAM-1. Very little VCAM-1 was released from endotoxin-stimulated HMEC-1, and sICAM-1 seemed a better activation marker for these cells. During incubation of HUVEC in media with glucose concentrations of 5.6, 10.6 or 20.6 m m, VCAM-1 was released to the media in a dose-dependent way without changes in surface expression. ICAM-1 was not influenced by the glucose concentration. There are situations when VCAM-1 concentrations in the media do not mirror the surface expression on HUVEC in culture, indicating that measurements of soluble adhesion molecules may not necessarily be representative of the conditions on the cell surface. Endothelium from different locations showed varying responses with respect to VCAM-1 and ICAM-1 liberation upon endotoxin stimulation. Thus, both sVCAM-1 and sICAM-1 should be quantified in clinical studies of endothelial activation until their characteristics are better clarified.</description><identifier>ISSN: 0300-9475</identifier><identifier>EISSN: 1365-3083</identifier><identifier>DOI: 10.1111/j.1365-3083.2008.02029.x</identifier><identifier>PMID: 18363595</identifier><language>eng</language><publisher>Oxford, UK: Oxford, UK : Blackwell Publishing Ltd</publisher><subject>Cells, Cultured ; Endothelial Cells - drug effects ; Endothelial Cells - immunology ; Endotoxins - pharmacology ; Humans ; Intercellular Adhesion Molecule-1 - genetics ; Intercellular Adhesion Molecule-1 - metabolism ; RNA, Messenger - genetics ; Solubility ; Umbilical Veins - immunology ; Vascular Cell Adhesion Molecule-1 - genetics ; Vascular Cell Adhesion Molecule-1 - metabolism</subject><ispartof>Scandinavian journal of immunology, 2008-05, Vol.67 (5), p.523-531</ispartof><rights>2008 The Authors</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4729-30edb88242c60e1e462df1d5b00d32c8281df4dbf5a627f20a6f5dd995dc48f83</citedby><cites>FETCH-LOGICAL-c4729-30edb88242c60e1e462df1d5b00d32c8281df4dbf5a627f20a6f5dd995dc48f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-3083.2008.02029.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-3083.2008.02029.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18363595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Videm, V</creatorcontrib><creatorcontrib>Albrigtsen, M</creatorcontrib><title>Soluble ICAM-1 and VCAM-1 as Markers of Endothelial Activation</title><title>Scandinavian journal of immunology</title><addtitle>Scand J Immunol</addtitle><description>Activated endothelium releases the soluble adhesion molecules vascular cell adhesion molecule-1 (sVCAM-1) and intercellular adhesion molecule-1 (sICAM-1). Measurement of fluid-phase adhesion molecules is therefore used to quantify endothelial activation, but it is unclear which is the better marker. The aims of the study were to compare the relationships between mRNA, surface and total expression and released VCAM-1 and ICAM-1 in endothelial cell cultures during activation, and to compare human umbilical vein endothelial cells (HUVEC) with the microvascular cell line HMEC-1. sVCAM-1 better represented mRNA and surface expression changes in HUVEC undergoing endotoxin stimulation than did sICAM-1. Very little VCAM-1 was released from endotoxin-stimulated HMEC-1, and sICAM-1 seemed a better activation marker for these cells. During incubation of HUVEC in media with glucose concentrations of 5.6, 10.6 or 20.6 m m, VCAM-1 was released to the media in a dose-dependent way without changes in surface expression. ICAM-1 was not influenced by the glucose concentration. There are situations when VCAM-1 concentrations in the media do not mirror the surface expression on HUVEC in culture, indicating that measurements of soluble adhesion molecules may not necessarily be representative of the conditions on the cell surface. Endothelium from different locations showed varying responses with respect to VCAM-1 and ICAM-1 liberation upon endotoxin stimulation. Thus, both sVCAM-1 and sICAM-1 should be quantified in clinical studies of endothelial activation until their characteristics are better clarified.</description><subject>Cells, Cultured</subject><subject>Endothelial Cells - drug effects</subject><subject>Endothelial Cells - immunology</subject><subject>Endotoxins - pharmacology</subject><subject>Humans</subject><subject>Intercellular Adhesion Molecule-1 - genetics</subject><subject>Intercellular Adhesion Molecule-1 - metabolism</subject><subject>RNA, Messenger - genetics</subject><subject>Solubility</subject><subject>Umbilical Veins - immunology</subject><subject>Vascular Cell Adhesion Molecule-1 - genetics</subject><subject>Vascular Cell Adhesion Molecule-1 - metabolism</subject><issn>0300-9475</issn><issn>1365-3083</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUFPwyAYhonRuDn9C9qTt9YPKC0cNFmWqTNbPMx5JbSAdnbrLK1u_97WLnpULnwJz_tCHhDyMAS4WVfLANOI-RQ4DQgAD4AAEcH2APV_Dg5RHyiAL8KY9dCJc0sATElMj1EPcxpRJlgf3cyLvE5y401Gw5mPPbXW3vN-dN5MlW-mdF5hvfFaF9WryTOVe8O0yj5UlRXrU3RkVe7M2X4foMXt-Gl0708f75rGqZ-GMRHNe4xOOCchSSMw2IQR0RZrlgBoSlJOONY21IllKiKxJaAiy7QWguk05JbTAbrsejdl8V4bV8lV5lKT52ptitrJGEIhiBB_ggQiEWPWNvIOTMvCudJYuSmzlSp3EoNsJculbF3K1qVsJctvyXLbRM_3d9TJyujf4N5qA1x3wGeWm92_i-X8YdJOTf6iy1tVSPVSZk4u5qT5vQbmFEJGvwD5EZD0</recordid><startdate>200805</startdate><enddate>200805</enddate><creator>Videm, V</creator><creator>Albrigtsen, M</creator><general>Oxford, UK : Blackwell Publishing Ltd</general><general>Blackwell Publishing Ltd</general><scope>FBQ</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>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>200805</creationdate><title>Soluble ICAM-1 and VCAM-1 as Markers of Endothelial Activation</title><author>Videm, V ; Albrigtsen, M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4729-30edb88242c60e1e462df1d5b00d32c8281df4dbf5a627f20a6f5dd995dc48f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Cells, Cultured</topic><topic>Endothelial Cells - drug effects</topic><topic>Endothelial Cells - immunology</topic><topic>Endotoxins - pharmacology</topic><topic>Humans</topic><topic>Intercellular Adhesion Molecule-1 - genetics</topic><topic>Intercellular Adhesion Molecule-1 - metabolism</topic><topic>RNA, Messenger - genetics</topic><topic>Solubility</topic><topic>Umbilical Veins - immunology</topic><topic>Vascular Cell Adhesion Molecule-1 - genetics</topic><topic>Vascular Cell Adhesion Molecule-1 - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Videm, V</creatorcontrib><creatorcontrib>Albrigtsen, M</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Scandinavian journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Videm, V</au><au>Albrigtsen, M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Soluble ICAM-1 and VCAM-1 as Markers of Endothelial Activation</atitle><jtitle>Scandinavian journal of immunology</jtitle><addtitle>Scand J Immunol</addtitle><date>2008-05</date><risdate>2008</risdate><volume>67</volume><issue>5</issue><spage>523</spage><epage>531</epage><pages>523-531</pages><issn>0300-9475</issn><eissn>1365-3083</eissn><abstract>Activated endothelium releases the soluble adhesion molecules vascular cell adhesion molecule-1 (sVCAM-1) and intercellular adhesion molecule-1 (sICAM-1). Measurement of fluid-phase adhesion molecules is therefore used to quantify endothelial activation, but it is unclear which is the better marker. The aims of the study were to compare the relationships between mRNA, surface and total expression and released VCAM-1 and ICAM-1 in endothelial cell cultures during activation, and to compare human umbilical vein endothelial cells (HUVEC) with the microvascular cell line HMEC-1. sVCAM-1 better represented mRNA and surface expression changes in HUVEC undergoing endotoxin stimulation than did sICAM-1. Very little VCAM-1 was released from endotoxin-stimulated HMEC-1, and sICAM-1 seemed a better activation marker for these cells. During incubation of HUVEC in media with glucose concentrations of 5.6, 10.6 or 20.6 m m, VCAM-1 was released to the media in a dose-dependent way without changes in surface expression. ICAM-1 was not influenced by the glucose concentration. There are situations when VCAM-1 concentrations in the media do not mirror the surface expression on HUVEC in culture, indicating that measurements of soluble adhesion molecules may not necessarily be representative of the conditions on the cell surface. Endothelium from different locations showed varying responses with respect to VCAM-1 and ICAM-1 liberation upon endotoxin stimulation. Thus, both sVCAM-1 and sICAM-1 should be quantified in clinical studies of endothelial activation until their characteristics are better clarified.</abstract><cop>Oxford, UK</cop><pub>Oxford, UK : Blackwell Publishing Ltd</pub><pmid>18363595</pmid><doi>10.1111/j.1365-3083.2008.02029.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0300-9475
ispartof Scandinavian journal of immunology, 2008-05, Vol.67 (5), p.523-531
issn 0300-9475
1365-3083
language eng
recordid cdi_proquest_miscellaneous_70499299
source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Access via Wiley Online Library; IngentaConnect Free/Open Access Journals; Wiley Online Library (Open Access Collection)
subjects Cells, Cultured
Endothelial Cells - drug effects
Endothelial Cells - immunology
Endotoxins - pharmacology
Humans
Intercellular Adhesion Molecule-1 - genetics
Intercellular Adhesion Molecule-1 - metabolism
RNA, Messenger - genetics
Solubility
Umbilical Veins - immunology
Vascular Cell Adhesion Molecule-1 - genetics
Vascular Cell Adhesion Molecule-1 - metabolism
title Soluble ICAM-1 and VCAM-1 as Markers of Endothelial Activation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T23%3A43%3A55IST&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=Soluble%20ICAM-1%20and%20VCAM-1%20as%20Markers%20of%20Endothelial%20Activation&rft.jtitle=Scandinavian%20journal%20of%20immunology&rft.au=Videm,%20V&rft.date=2008-05&rft.volume=67&rft.issue=5&rft.spage=523&rft.epage=531&rft.pages=523-531&rft.issn=0300-9475&rft.eissn=1365-3083&rft_id=info:doi/10.1111/j.1365-3083.2008.02029.x&rft_dat=%3Cproquest_cross%3E20697158%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=20697158&rft_id=info:pmid/18363595&rfr_iscdi=true