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...

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Veröffentlicht in:Transfusion clinique et biologique (Paris) 2006-03, Vol.13 (1), p.44-49
Hauptverfasser: Delahunty, M., Zennadi, R., Telen, M.J.
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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
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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. 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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. 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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. 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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>
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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
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