NF-kappaB inhibitors impair platelet activation responses

• Published in: Journal of thrombosis and haemostasis Vol. 7; no. 8; pp. 1333 - 1343
• Main Authors: Malaver, E, Romaniuk, M A, D'Atri, L P, Pozner, R G, Negrotto, S, Benzadón, R, Schattner, M
• Format: Journal Article
• Language: English
• Published: England 01-08-2009
• Subjects: Animals; Cells, Cultured; Dual Specificity Phosphatase 2; Fibrinogen - metabolism; Humans; I-kappa B Proteins - metabolism; Mice; NF-kappa B - antagonists & inhibitors; NF-kappa B - metabolism; NF-kappa B - physiology; NF-KappaB Inhibitor alpha; Phosphorylation; Platelet Activation; Platelet Adhesiveness; Protein Binding
• ISSN: 1538-7836
• DOI: 10.1111/j.1538-7836.2009.03492.x

Although platelets are anucleated cells, they express several transcription factors that exert non-genomic functions, including the positive and negative regulation of platelet activation. NF-kappaB is a major transcriptional regulator of genes involved in survival, proliferation and inflammation.
Because platelets play a critical role not only in hemostasis, but also in inflammation and tumor progression, we evaluated the role of NF-kappaB in platelet physiology.
Immunofluorescence, Western blotting and ELISA studies revealed that platelets express IkappaBalpha and NF-kappaB, and that stimulation with thrombin triggers IkappaBalpha phosphorylation and degradation and the binding of platelet NF-kappaB p65 subunit to synthetic oligonucleotides containing the consensus sequence for NF-kappaB. Two specific unrelated inhibitors of NF-kappaB activation, BAY 11-7082 and Ro 106-9920, reduced PAC-1 and fibrinogen binding to integrin alpha(IIb)beta3 and restricted platelet spreading on immobilized fibrinogen. Both inhibitors impaired aggregation mediated by ADP, epinephrine, collagen or thrombin, but not arachidonic acid. ATP release, TXB2 formation, P-selectin expression, ERK phosphorylation and cPLA2 activity stimulated by thrombin were reduced in BAY 11-7082- or Ro 106-9920-treated platelets. Although bleeding time was not affected, ADP-induced platelet aggregation was impaired in mice treated with BAY 11-7082.
Our results suggest that NF-kappaB may be a novel mediator of platelet responses. The blockade of platelet function by NF-kappaB inhibitors might be relevant in those clinical situations where these drugs are being considered for anti-tumor and/or anti-inflammatory therapy.