LW protein: a promiscuous integrin receptor activated by adrenergic signaling
The LW blood group antigen glycoprotein, although part of the Rh macromolecular complex, is nonetheless a member of the intercellular adhesion molecule (ICAM) family. Thus, while it is only rarely clinically important in the setting of transfusion and pregnancy, LW is likely to contribute to red cel...
Gespeichert in:
Veröffentlicht in: | Transfusion clinique et biologique (Paris) 2006-03, Vol.13 (1), p.44-49 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 49 |
---|---|
container_issue | 1 |
container_start_page | 44 |
container_title | Transfusion clinique et biologique (Paris) |
container_volume | 13 |
creator | Delahunty, M. Zennadi, R. Telen, M.J. |
description | The LW blood group antigen glycoprotein, although part of the Rh macromolecular complex, is nonetheless a member of the intercellular adhesion molecule (ICAM) family. Thus, while it is only rarely clinically important in the setting of transfusion and pregnancy, LW is likely to contribute to red cell adhesion in a variety of settings, including during hematopoiesis, as well as in vascular disorders. The best documentation of a pathophysiological role for LW in human disease is in sickle cell disease, where it contributes to red cell adhesion to endothelial cells and the development of vaso-occlusion, the hallmark of that disease. LW may also contribute to other intravascular processes, such as both venous and arterial thrombosis, due to its ability to interact with both activated platelets as well as leukocytes. The evidence that LW itself can undergo activation on red cells holds promise that pharmacotherapeutic maneuvers may be found to prevent such pathophysiologic interactions. |
doi_str_mv | 10.1016/j.tracli.2006.02.022 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67896677</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1246782006000231</els_id><sourcerecordid>67896677</sourcerecordid><originalsourceid>FETCH-LOGICAL-c390t-c97aa472306d658ba5e2e1886dd3c3da922515a85ac024f290e586bbac7bc32b3</originalsourceid><addsrcrecordid>eNp9kM9KAzEQh3NQbK2-gche9NY1yXaTXQ-CFP9BoRfFY5hNpiVlm61JWujb9Fn6ZKa04E0YmDl8M_PjI-SG0ZxRJh4WefSgW5tzSkVOeSp-RvqMj8RQVpz2yGUIC0qZZLW8ID0mSjGSXPTJdPKdrXwX0brHDPa7NC9t0OtuHTLrIs69dZlHjavY-Qx0tBuIaLJmu9-B8ejQz63Ogp07aK2bX5HzGbQBr099QL5eXz7H78PJ9O1j_DwZ6qKmcahrCZASFFQYUVYNlMiRVZUwptCFgZrzkpVQlaApH814TbGsRNOAlo0ueFMMyP3xbgr8s8YQ1SE2ti04TNmVkFUthJQJHB1B7bsQPM7Uytsl-K1iVB3kqYU6ylMHeYryVDyt3Z7ur5slmr-lk7kE3J0ACBramQenbfjjpGRMFof_T0cOk42NRa-Ctug0Gpu0RmU6-3-SX12Nk7A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67896677</pqid></control><display><type>article</type><title>LW protein: a promiscuous integrin receptor activated by adrenergic signaling</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Delahunty, M. ; Zennadi, R. ; Telen, M.J.</creator><creatorcontrib>Delahunty, M. ; Zennadi, R. ; Telen, M.J.</creatorcontrib><description>The LW blood group antigen glycoprotein, although part of the Rh macromolecular complex, is nonetheless a member of the intercellular adhesion molecule (ICAM) family. Thus, while it is only rarely clinically important in the setting of transfusion and pregnancy, LW is likely to contribute to red cell adhesion in a variety of settings, including during hematopoiesis, as well as in vascular disorders. The best documentation of a pathophysiological role for LW in human disease is in sickle cell disease, where it contributes to red cell adhesion to endothelial cells and the development of vaso-occlusion, the hallmark of that disease. LW may also contribute to other intravascular processes, such as both venous and arterial thrombosis, due to its ability to interact with both activated platelets as well as leukocytes. The evidence that LW itself can undergo activation on red cells holds promise that pharmacotherapeutic maneuvers may be found to prevent such pathophysiologic interactions.</description><identifier>ISSN: 1246-7820</identifier><identifier>DOI: 10.1016/j.tracli.2006.02.022</identifier><identifier>PMID: 16564726</identifier><language>eng</language><publisher>Paris: Elsevier SAS</publisher><subject>Adhérence cellulaire ; Adrenergic signaling ; Alleles ; Anemia, Sickle Cell - physiopathology ; Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Biological and medical sciences ; Blood and lymphatic vessels ; Blood group ; Blood Group Antigens - genetics ; Blood Platelets - metabolism ; Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis ; Blood. Blood coagulation. Reticuloendothelial system ; Cardiology. Vascular system ; Cell adhesion ; Cell Adhesion - physiology ; Cell Adhesion Molecules - drug effects ; Cell Adhesion Molecules - genetics ; Cell Adhesion Molecules - physiology ; Chromosomes, Human, Pair 9 - genetics ; Cyclic AMP - physiology ; Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous ; Drépanocytose ; Endothelium, Vascular - pathology ; Epinephrine - pharmacology ; Erythrocytes - metabolism ; Erythrocytes - physiology ; Groupes sanguins ; Humans ; ICAM-4 ; Integrin alphaV - metabolism ; Integrin receptor ; Lymphocyte Function-Associated Antigen-1 - metabolism ; Medical sciences ; Pharmacology. Drug treatments ; Phosphorylation - drug effects ; Platelet Glycoprotein GPIIb-IIIa Complex - metabolism ; Polymorphism, Single Nucleotide ; Protein Processing, Post-Translational - drug effects ; Receptors, Adrenergic, beta - drug effects ; Receptors, Adrenergic, beta - physiology ; Rh-Hr Blood-Group System - physiology ; Récepteur d'intégrines ; Sickle cell disease ; Signal Transduction - drug effects ; Signalisation adrénergique ; Thrombosis - physiopathology ; Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><ispartof>Transfusion clinique et biologique (Paris), 2006-03, Vol.13 (1), p.44-49</ispartof><rights>2006 Elsevier SAS</rights><rights>2006 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c390t-c97aa472306d658ba5e2e1886dd3c3da922515a85ac024f290e586bbac7bc32b3</citedby><cites>FETCH-LOGICAL-c390t-c97aa472306d658ba5e2e1886dd3c3da922515a85ac024f290e586bbac7bc32b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S1246782006000231$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>309,310,314,776,780,785,786,3537,23909,23910,25118,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=17711737$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16564726$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Delahunty, M.</creatorcontrib><creatorcontrib>Zennadi, R.</creatorcontrib><creatorcontrib>Telen, M.J.</creatorcontrib><title>LW protein: a promiscuous integrin receptor activated by adrenergic signaling</title><title>Transfusion clinique et biologique (Paris)</title><addtitle>Transfus Clin Biol</addtitle><description>The LW blood group antigen glycoprotein, although part of the Rh macromolecular complex, is nonetheless a member of the intercellular adhesion molecule (ICAM) family. Thus, while it is only rarely clinically important in the setting of transfusion and pregnancy, LW is likely to contribute to red cell adhesion in a variety of settings, including during hematopoiesis, as well as in vascular disorders. The best documentation of a pathophysiological role for LW in human disease is in sickle cell disease, where it contributes to red cell adhesion to endothelial cells and the development of vaso-occlusion, the hallmark of that disease. LW may also contribute to other intravascular processes, such as both venous and arterial thrombosis, due to its ability to interact with both activated platelets as well as leukocytes. The evidence that LW itself can undergo activation on red cells holds promise that pharmacotherapeutic maneuvers may be found to prevent such pathophysiologic interactions.</description><subject>Adhérence cellulaire</subject><subject>Adrenergic signaling</subject><subject>Alleles</subject><subject>Anemia, Sickle Cell - physiopathology</subject><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Blood group</subject><subject>Blood Group Antigens - genetics</subject><subject>Blood Platelets - metabolism</subject><subject>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</subject><subject>Blood. Blood coagulation. Reticuloendothelial system</subject><subject>Cardiology. Vascular system</subject><subject>Cell adhesion</subject><subject>Cell Adhesion - physiology</subject><subject>Cell Adhesion Molecules - drug effects</subject><subject>Cell Adhesion Molecules - genetics</subject><subject>Cell Adhesion Molecules - physiology</subject><subject>Chromosomes, Human, Pair 9 - genetics</subject><subject>Cyclic AMP - physiology</subject><subject>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</subject><subject>Drépanocytose</subject><subject>Endothelium, Vascular - pathology</subject><subject>Epinephrine - pharmacology</subject><subject>Erythrocytes - metabolism</subject><subject>Erythrocytes - physiology</subject><subject>Groupes sanguins</subject><subject>Humans</subject><subject>ICAM-4</subject><subject>Integrin alphaV - metabolism</subject><subject>Integrin receptor</subject><subject>Lymphocyte Function-Associated Antigen-1 - metabolism</subject><subject>Medical sciences</subject><subject>Pharmacology. Drug treatments</subject><subject>Phosphorylation - drug effects</subject><subject>Platelet Glycoprotein GPIIb-IIIa Complex - metabolism</subject><subject>Polymorphism, Single Nucleotide</subject><subject>Protein Processing, Post-Translational - drug effects</subject><subject>Receptors, Adrenergic, beta - drug effects</subject><subject>Receptors, Adrenergic, beta - physiology</subject><subject>Rh-Hr Blood-Group System - physiology</subject><subject>Récepteur d'intégrines</subject><subject>Sickle cell disease</subject><subject>Signal Transduction - drug effects</subject><subject>Signalisation adrénergique</subject><subject>Thrombosis - physiopathology</subject><subject>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</subject><issn>1246-7820</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kM9KAzEQh3NQbK2-gche9NY1yXaTXQ-CFP9BoRfFY5hNpiVlm61JWujb9Fn6ZKa04E0YmDl8M_PjI-SG0ZxRJh4WefSgW5tzSkVOeSp-RvqMj8RQVpz2yGUIC0qZZLW8ID0mSjGSXPTJdPKdrXwX0brHDPa7NC9t0OtuHTLrIs69dZlHjavY-Qx0tBuIaLJmu9-B8ejQz63Ogp07aK2bX5HzGbQBr099QL5eXz7H78PJ9O1j_DwZ6qKmcahrCZASFFQYUVYNlMiRVZUwptCFgZrzkpVQlaApH814TbGsRNOAlo0ueFMMyP3xbgr8s8YQ1SE2ti04TNmVkFUthJQJHB1B7bsQPM7Uytsl-K1iVB3kqYU6ylMHeYryVDyt3Z7ur5slmr-lk7kE3J0ACBramQenbfjjpGRMFof_T0cOk42NRa-Ctug0Gpu0RmU6-3-SX12Nk7A</recordid><startdate>20060301</startdate><enddate>20060301</enddate><creator>Delahunty, M.</creator><creator>Zennadi, R.</creator><creator>Telen, M.J.</creator><general>Elsevier SAS</general><general>Elsevier</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><scope>7X8</scope></search><sort><creationdate>20060301</creationdate><title>LW protein: a promiscuous integrin receptor activated by adrenergic signaling</title><author>Delahunty, M. ; Zennadi, R. ; Telen, M.J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c390t-c97aa472306d658ba5e2e1886dd3c3da922515a85ac024f290e586bbac7bc32b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adhérence cellulaire</topic><topic>Adrenergic signaling</topic><topic>Alleles</topic><topic>Anemia, Sickle Cell - physiopathology</topic><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Blood group</topic><topic>Blood Group Antigens - genetics</topic><topic>Blood Platelets - metabolism</topic><topic>Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis</topic><topic>Blood. Blood coagulation. Reticuloendothelial system</topic><topic>Cardiology. Vascular system</topic><topic>Cell adhesion</topic><topic>Cell Adhesion - physiology</topic><topic>Cell Adhesion Molecules - drug effects</topic><topic>Cell Adhesion Molecules - genetics</topic><topic>Cell Adhesion Molecules - physiology</topic><topic>Chromosomes, Human, Pair 9 - genetics</topic><topic>Cyclic AMP - physiology</topic><topic>Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous</topic><topic>Drépanocytose</topic><topic>Endothelium, Vascular - pathology</topic><topic>Epinephrine - pharmacology</topic><topic>Erythrocytes - metabolism</topic><topic>Erythrocytes - physiology</topic><topic>Groupes sanguins</topic><topic>Humans</topic><topic>ICAM-4</topic><topic>Integrin alphaV - metabolism</topic><topic>Integrin receptor</topic><topic>Lymphocyte Function-Associated Antigen-1 - metabolism</topic><topic>Medical sciences</topic><topic>Pharmacology. Drug treatments</topic><topic>Phosphorylation - drug effects</topic><topic>Platelet Glycoprotein GPIIb-IIIa Complex - metabolism</topic><topic>Polymorphism, Single Nucleotide</topic><topic>Protein Processing, Post-Translational - drug effects</topic><topic>Receptors, Adrenergic, beta - drug effects</topic><topic>Receptors, Adrenergic, beta - physiology</topic><topic>Rh-Hr Blood-Group System - physiology</topic><topic>Récepteur d'intégrines</topic><topic>Sickle cell disease</topic><topic>Signal Transduction - drug effects</topic><topic>Signalisation adrénergique</topic><topic>Thrombosis - physiopathology</topic><topic>Transfusions. Complications. Transfusion reactions. Cell and gene therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Delahunty, M.</creatorcontrib><creatorcontrib>Zennadi, R.</creatorcontrib><creatorcontrib>Telen, M.J.</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><collection>MEDLINE - Academic</collection><jtitle>Transfusion clinique et biologique (Paris)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Delahunty, M.</au><au>Zennadi, R.</au><au>Telen, M.J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>LW protein: a promiscuous integrin receptor activated by adrenergic signaling</atitle><jtitle>Transfusion clinique et biologique (Paris)</jtitle><addtitle>Transfus Clin Biol</addtitle><date>2006-03-01</date><risdate>2006</risdate><volume>13</volume><issue>1</issue><spage>44</spage><epage>49</epage><pages>44-49</pages><issn>1246-7820</issn><abstract>The LW blood group antigen glycoprotein, although part of the Rh macromolecular complex, is nonetheless a member of the intercellular adhesion molecule (ICAM) family. Thus, while it is only rarely clinically important in the setting of transfusion and pregnancy, LW is likely to contribute to red cell adhesion in a variety of settings, including during hematopoiesis, as well as in vascular disorders. The best documentation of a pathophysiological role for LW in human disease is in sickle cell disease, where it contributes to red cell adhesion to endothelial cells and the development of vaso-occlusion, the hallmark of that disease. LW may also contribute to other intravascular processes, such as both venous and arterial thrombosis, due to its ability to interact with both activated platelets as well as leukocytes. The evidence that LW itself can undergo activation on red cells holds promise that pharmacotherapeutic maneuvers may be found to prevent such pathophysiologic interactions.</abstract><cop>Paris</cop><pub>Elsevier SAS</pub><pmid>16564726</pmid><doi>10.1016/j.tracli.2006.02.022</doi><tpages>6</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1246-7820 |
ispartof | Transfusion clinique et biologique (Paris), 2006-03, Vol.13 (1), p.44-49 |
issn | 1246-7820 |
language | eng |
recordid | cdi_proquest_miscellaneous_67896677 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Adhérence cellulaire Adrenergic signaling Alleles Anemia, Sickle Cell - physiopathology Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Biological and medical sciences Blood and lymphatic vessels Blood group Blood Group Antigens - genetics Blood Platelets - metabolism Blood. Blood and plasma substitutes. Blood products. Blood cells. Blood typing. Plasmapheresis. Apheresis Blood. Blood coagulation. Reticuloendothelial system Cardiology. Vascular system Cell adhesion Cell Adhesion - physiology Cell Adhesion Molecules - drug effects Cell Adhesion Molecules - genetics Cell Adhesion Molecules - physiology Chromosomes, Human, Pair 9 - genetics Cyclic AMP - physiology Diseases of the peripheral vessels. Diseases of the vena cava. Miscellaneous Drépanocytose Endothelium, Vascular - pathology Epinephrine - pharmacology Erythrocytes - metabolism Erythrocytes - physiology Groupes sanguins Humans ICAM-4 Integrin alphaV - metabolism Integrin receptor Lymphocyte Function-Associated Antigen-1 - metabolism Medical sciences Pharmacology. Drug treatments Phosphorylation - drug effects Platelet Glycoprotein GPIIb-IIIa Complex - metabolism Polymorphism, Single Nucleotide Protein Processing, Post-Translational - drug effects Receptors, Adrenergic, beta - drug effects Receptors, Adrenergic, beta - physiology Rh-Hr Blood-Group System - physiology Récepteur d'intégrines Sickle cell disease Signal Transduction - drug effects Signalisation adrénergique Thrombosis - physiopathology Transfusions. Complications. Transfusion reactions. Cell and gene therapy |
title | LW protein: a promiscuous integrin receptor activated by adrenergic signaling |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T13%3A19%3A01IST&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=LW%20protein:%20a%C2%A0promiscuous%20integrin%20receptor%20activated%20by%C2%A0adrenergic%20signaling&rft.jtitle=Transfusion%20clinique%20et%20biologique%20(Paris)&rft.au=Delahunty,%20M.&rft.date=2006-03-01&rft.volume=13&rft.issue=1&rft.spage=44&rft.epage=49&rft.pages=44-49&rft.issn=1246-7820&rft_id=info:doi/10.1016/j.tracli.2006.02.022&rft_dat=%3Cproquest_cross%3E67896677%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=67896677&rft_id=info:pmid/16564726&rft_els_id=S1246782006000231&rfr_iscdi=true |