Source:http://linkedlifedata.com/resource/pubmed/id/15226180
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2004-10-6
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pubmed:abstractText |
The tetraspanin family member CD151 forms complexes with integrins and regulates cell adhesion and migration. While CD151 is highly expressed in megakaryocytes and to a lesser extent in platelets, its physiologic role in platelets is unclear. In this study, we investigate the physical and functional importance of CD151 in murine platelets. Immunoprecipitation/Western blot studies reveal a constitutive physical association of CD151 with integrin alpha(IIb)beta(3) complex under strong detergent conditions. Using CD151-deficient mice, we show that the platelets have impaired "outside-in" integrin alpha(IIb)beta(3) signaling with defective platelet aggregation responses to protease-activated receptor 4 (PAR-4) agonist peptide, collagen, and adenosine diphosphate (ADP); impaired platelet spreading on fibrinogen; and delayed kinetics of clot retraction in vitro. This functional integrin alpha(IIb)beta(3) defect could not be attributed to altered expression of integrin alpha(IIb)beta(3). CD151(-/-) platelets displayed normal platelet alpha granule secretion, dense granule secretion, and static platelet adhesion. In addition, CD151(-/-) platelets displayed normal "inside-out" integrin alpha(IIb)beta(3) signaling properties as demonstrated by normal agonist-induced binding of soluble fluorescein isothiocyanate (FITC)-fibrinogen, JON/A antibody binding, and increases in cytosolic-free calcium and inositol 1,4,5 triphosphate (IP(3)) levels. This study provides the first direct evidence that CD151 is essential for normal platelet function and that disruption of CD151 induced a moderate outside-in integrin alpha(IIb)beta(3) signaling defect.
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pubmed:commentsCorrections | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD151,
http://linkedlifedata.com/resource/pubmed/chemical/CD151 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Cd151 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Platelet Glycoprotein GPIIb-IIIa...
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0006-4971
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
15
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pubmed:volume |
104
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2368-75
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pubmed:dateRevised |
2011-11-17
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pubmed:meshHeading |
pubmed-meshheading:15226180-Animals,
pubmed-meshheading:15226180-Antigens, CD,
pubmed-meshheading:15226180-Antigens, CD151,
pubmed-meshheading:15226180-Blood Platelets,
pubmed-meshheading:15226180-Cell Adhesion,
pubmed-meshheading:15226180-Cytoskeleton,
pubmed-meshheading:15226180-Humans,
pubmed-meshheading:15226180-Mice,
pubmed-meshheading:15226180-Mice, Knockout,
pubmed-meshheading:15226180-Platelet Aggregation,
pubmed-meshheading:15226180-Platelet Glycoprotein GPIIb-IIIa Complex,
pubmed-meshheading:15226180-Protein Binding,
pubmed-meshheading:15226180-Secretory Vesicles,
pubmed-meshheading:15226180-Signal Transduction
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pubmed:year |
2004
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pubmed:articleTitle |
The tetraspanin superfamily member CD151 regulates outside-in integrin alphaIIbbeta3 signaling and platelet function.
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pubmed:affiliation |
Kronheimer Building, Austin Research Institute, Austin Hospital, Studley Rd, Heidelberg, Victoria 3084 Australia.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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