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Activated human platelets induce factor XIIa-mediated contact activation

Bäck, Jennie (författare)
Uppsala universitet,Enheten för klinisk immunologi
Sanchez, Javier (författare)
Uppsala universitet,Enheten för klinisk immunologi
Elgue, Graciela (författare)
Uppsala universitet,Enheten för klinisk immunologi
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Ekdahl, Kristina Nilsson (författare)
Linnéuniversitetet,Uppsala universitet,Enheten för klinisk immunologi,Institutionen för naturvetenskap, NV
Nilsson, Bo (författare)
Uppsala universitet,Enheten för klinisk immunologi
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 (creator_code:org_t)
Elsevier BV, 2010
2010
Engelska.
Ingår i: Biochemical and Biophysical Research Communications - BBRC. - : Elsevier BV. - 0006-291X .- 1090-2104. ; 391:1, s. 11-17
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Earlier studies have shown that isolated platelets in buffer systems can promote activation of FXII or amplify contact activation, in the presence of a negatively charge substance or material. Still proof is lacking that FXII is activated by platelets in a more physiological environment. In this study we investigate if activated platelets can induce FXII-mediated contact activation and whether this activation affects clot formation in human blood. Human platelets were activated with a thrombin receptor-activating peptide, SFLLRN-amide, in platelet-rich plasma or in whole blood. FXIIa and FXIa in complex with preferentially antithrombin (AT) and to some extent C1-inhibitor (C1INH) were generated in response to TRAP stimulation. This contact activation was independent of surface-mediated contact activation, tissue factor pathway or thrombin. In clotting whole blood FXIIa-AT and FXIa-AT complexes were specifically formed, demonstrating that AT is a potent inhibitor of FXIIa and FXIa generated by platelet activation. Contact activation proteins were analyzed by flow cytometry and FXII, FXI, high-molecular weight kininogen, and prekallikrein were detected on activated platelets. Using chromogenic assays, enzymatic activity of platelet-associated FXIIa, FXIa, and kallikrein were demonstrated. Inhibition of FXIIa in non-anticoagulated blood also prolonged the clotting time. We conclude that platelet activation triggers FXII-mediated contact activation on the surface and in the vicinity of activated platelets. This leads specifically to generation of FXIIa-AT and FXIa-AT complexes, and contributes to clot formation. Activated platelets may thereby constitute an intravascular locus for contact activation, which may explain the recently reported importance of FXII in thrombus formation.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper -- Immunologi inom det medicinska området (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine -- Immunology in the medical area (hsv//eng)

Nyckelord

Antithrombin
Clot formation
Contact activation
Factor XII
Platelets
MEDICINE
MEDICIN
Immunology
Immunologi

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