Pregled bibliografske jedinice broj: 712184
Potent inhibition of human platelets by cGMP analogs independent of cGMP-dependent protein kinase
Potent inhibition of human platelets by cGMP analogs independent of cGMP-dependent protein kinase // Blood, 103 (2004), 7; 2593-2600 (međunarodna recenzija, članak, znanstveni)
CROSBI ID: 712184 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Potent inhibition of human platelets by cGMP analogs independent of cGMP-dependent protein kinase
Autori
Gambaryan, Stepan ; Geiger, Joerg ; Schwarz, Ulrike R ; Butt, Elke, Begonja, Antonija ; Obergfell, Achim ; Walter, Ulrich
Izvornik
Blood (0006-4971) 103
(2004), 7;
2593-2600
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni
Ključne riječi
cGMP; PKG; platelets; signal transduction
Sažetak
Platelets play a key role in hemostasis through their ability to rapidly adhere to activated or injured endothelium, subendothelial matrix proteins, and other activated platelets. A strong equilibrium between activating and inhibiting processes is essential for normal platelet and vascular function, impairment of this equilibrium being associated with either thrombophilic or bleeding disorders. Both cyclic guanosine monophosphate (cGMP) and cyclic adenosine monophosphate (cAMP) have been established as crucial and synergistic intracellular messengers that mediate the effects of platelet inhibitors such as nitric oxide (NO) and prostacyclin (PG-I2). However, it was recently suggested that a rapid cGMP/cGMP-dependent protein kinase (cGK)-mediated extracellular signal-related kinase (ERK) phosphorylation promotes platelet activation. This hypothesis was examined here by evaluating established and proposed cGK activators/inhibitors with respect to their capacity to promote either platelet activation or inhibition. In particular, the regulatory role of cGK for ERK phosphorylation and thrombin-, thromboxane-, and VWF-induced platelet activation was investigated. The data obtained do not support the concept that cGK-mediated ERK phosphorylation promotes platelet activation but confirm the inhibitory role of cGK in platelet function. One explanation for these discrepancies is the novel finding that extracellular cGMP analogs potently and rapidly inhibit thrombin-, thromboxane-, and VWF-induced human platelet signaling and activation by a cGK-independent mechanism.
Izvorni jezik
Engleski
Znanstvena područja
Biologija, Temeljne medicinske znanosti
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE