Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2006-4-24
pubmed:abstractText
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.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Blood Group Antigens, http://linkedlifedata.com/resource/pubmed/chemical/Cell Adhesion Molecules, http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP, http://linkedlifedata.com/resource/pubmed/chemical/Epinephrine, http://linkedlifedata.com/resource/pubmed/chemical/ICAM4 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Integrin alphaV, http://linkedlifedata.com/resource/pubmed/chemical/Lymphocyte Function-Associated..., http://linkedlifedata.com/resource/pubmed/chemical/Platelet Glycoprotein GPIIb-IIIa..., http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Adrenergic, beta, http://linkedlifedata.com/resource/pubmed/chemical/Rh-Hr Blood-Group System, http://linkedlifedata.com/resource/pubmed/chemical/Rho(D) antigen
pubmed:status
MEDLINE
pubmed:issn
1246-7820
pubmed:author
pubmed:issnType
Print
pubmed:volume
13
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
44-9
pubmed:meshHeading
pubmed-meshheading:16564726-Alleles, pubmed-meshheading:16564726-Anemia, Sickle Cell, pubmed-meshheading:16564726-Blood Group Antigens, pubmed-meshheading:16564726-Blood Platelets, pubmed-meshheading:16564726-Cell Adhesion, pubmed-meshheading:16564726-Cell Adhesion Molecules, pubmed-meshheading:16564726-Chromosomes, Human, Pair 9, pubmed-meshheading:16564726-Cyclic AMP, pubmed-meshheading:16564726-Endothelium, Vascular, pubmed-meshheading:16564726-Epinephrine, pubmed-meshheading:16564726-Erythrocytes, pubmed-meshheading:16564726-Humans, pubmed-meshheading:16564726-Integrin alphaV, pubmed-meshheading:16564726-Lymphocyte Function-Associated Antigen-1, pubmed-meshheading:16564726-Phosphorylation, pubmed-meshheading:16564726-Platelet Glycoprotein GPIIb-IIIa Complex, pubmed-meshheading:16564726-Polymorphism, Single Nucleotide, pubmed-meshheading:16564726-Protein Processing, Post-Translational, pubmed-meshheading:16564726-Receptors, Adrenergic, beta, pubmed-meshheading:16564726-Rh-Hr Blood-Group System, pubmed-meshheading:16564726-Signal Transduction, pubmed-meshheading:16564726-Thrombosis
pubmed:articleTitle
LW protein: a promiscuous integrin receptor activated by adrenergic signaling.
pubmed:affiliation
Division of Hematology, Department of Medicine, Box 2615, Duke University Medical Center, Duke University, Durham, NC 27710, USA.
pubmed:publicationType
Journal Article, Review