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2003 | 50 | 4 |

Tytuł artykułu

Inhibition of collagen-induced platelet reactivity by DGEA peptide

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Direct interactions between collagen, the most thrombogenic component of the extracellular matrix, and platelet surface membrane receptors mediate platelet adhe­sion and induce platelet activation and aggregation. In this process two glyco- proteins are crucial: integrin a2β1, an adhesive receptor, and GPVI, which is espe­cially responsible for signal transduction. Specific antagonists of the collagen recep­tors are useful tools for investigating the complexity of platelet-collagen interactions. In this work we assessed the usefulness of DGEA peptide (Asp-Gly-Glu-Ala), the shortest collagen type I-derived motif recognised by the collagen-binding integrin a2β1, as a potential antagonist of collagen receptors. We examined platelet function using several methods including platelet adhesion under static conditions, platelet function analyser PFA-100™, whole blood electric impedance aggregometry (WBEA) and flow cytometry. We found that DGEA significantly inhibited adhesion, aggrega­tion and release reaction of collagen activated blood platelets. The inhibitory effect of DGEA on static platelet adhesion reached sub-maximal values at millimolar inhibi­tor concentrations, whereas the specific blocker of a2β1 — monoclonal antibodies Gi9, when used at saturating concentrations, had only a moderate inhibitory effect on platelet adhesion. Considering that 25-30% of total collagen binding to is specific, we conclude that DGEA is a strong antagonist interfering with a variety of collagen-platelet inter­actions, and it can be recognised not only by the primary platelet adhesion receptor but also by other collagen receptors.

Wydawca

-

Rocznik

Tom

50

Numer

4

Opis fizyczny

p.1119-1128,fig.,ref.

Twórcy

autor
  • Medical University of Lodz, Zeromskiego 113, 90-549 Lodz, Poland
autor
autor
autor
autor

Bibliografia

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Typ dokumentu

Bibliografia

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Identyfikator YADDA

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