Abstract
Platelet activation at sites of vascular injury is triggered through different signaling pathways leading to activation of phospholipase (PL) Cβ or PLCγ2. Active PLCs trigger Ca2+ mobilization and entry, which is a prerequisite for adhesion, secretion, and thrombus formation. PLCβ isoenzymes are activated downstream of G protein-coupled receptors (GPCRs), whereas PLCγ2 is activated downstream of immunoreceptor tyrosine-based activation motif (ITAM)-coupled receptors, such as the major platelet collagen receptor glycoprotein (GP) VI or CLEC-2. The mechanisms underlying PLC regulation are not fully understood. An involvement of small GTPases of the Rho family (Rho, Rac, Cdc42) in PLC activation has been proposed but this has not been investigated in platelets. We here show that murine platelets lacking Rac1 display severely impaired GPVI- or CLEC-2-dependent activation and aggregation. This defect was associated with impaired production of inositol 1,4,5-trisphosphate (IP3) and intracellular calcium mobilization suggesting inappropriate activation of PLCγ2 despite normal tyrosine phosphorylation of the enzyme. Rac1 −/− platelets displayed defective thrombus formation on collagen under flow conditions which could be fully restored by co-infusion of ADP and the TxA2 analog U46619, indicating that impaired GPVI-, but not G-protein signaling, was responsible for the observed defect. In line with this, Rac1 −/− mice were protected in two collagen-dependent arterial thrombosis models. Together, these results demonstrate that Rac1 is essential for ITAM-dependent PLCγ2 activation in platelets and that this is critical for thrombus formation in vivo.
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Abbreviations
- BSA:
-
bovine serum albumin
- CLEC-2:
-
C-type lectin-like receptor
- CRP:
-
collagen related peptide
- CVX:
-
convulxin
- FACS:
-
fluoresence activated cell sorting
- FcR:
-
Fc receptor
- FITC:
-
fluoresceine isothiocyanate
- GP:
-
glycoprotein
- HRP:
-
horseradish peroxidase
- Ig:
-
immunoglobulin
- PAGE:
-
polyacrylamide gel electrophoresis
- PLCγ2:
-
phospholipase Cγ2
- PMA:
-
phorbol 12-myristate 13-acetate
- prp:
-
platelet rich plasma
- PVDF:
-
polyvinylidene difluoride
- RC:
-
rhodocytin
- SDS:
-
sodium dodecyl sulfate
- TxA2 :
-
thromboxane A2
- vWF:
-
von Willebrand factor
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We would like to thank Sylvia Hengst for excellent technical assistance.
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Irina Pleines, Margitta Elvers, Amrei Strehl: these authors contributed equally to this work.
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Pleines, I., Elvers, M., Strehl, A. et al. Rac1 is essential for phospholipase C-γ2 activation in platelets. Pflugers Arch - Eur J Physiol 457, 1173–1185 (2009). https://doi.org/10.1007/s00424-008-0573-7
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DOI: https://doi.org/10.1007/s00424-008-0573-7