Potential and limitations of PKA/ PKG inhibitors for platelet studies
Autor: | Valentina Shpakova, Stepan Gambaryan, Ulrich Walter, Natalia Rukoyatkina |
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Rok vydání: | 2021 |
Předmět: |
Blood Platelets
Kinase Intracellular Signaling Peptides and Proteins Adenylate kinase Hematology General Medicine KT5720 Cyclic AMP-Dependent Protein Kinases chemistry.chemical_compound chemistry Biochemistry Cyclic AMP Cyclic GMP-Dependent Protein Kinases cardiovascular system Humans Platelet Platelet activation Protein kinase A Cyclic GMP cGMP-dependent protein kinase Intracellular |
Zdroj: | Platelets. 33:859-868 |
ISSN: | 1369-1635 0953-7104 |
DOI: | 10.1080/09537104.2021.2003316 |
Popis: | Cyclic nucleotides (cAMP and cGMP) and corresponding protein kinases, protein kinase A (PKA) and protein kinase G (PKG), are the main intracellular mediators of endothelium-derived platelet inhibitors. Pharmacological PKA/PKG inhibitors are often used to discriminate between these two kinase activities and to analyze their underlying mechanisms. Previously we showed that all widely used PKG inhibitors (KT5823, DT3, RP isomers) either did not inhibit PKG or inhibited and even activated platelets independently from PKG. In this study, we examined several PKA inhibitors as well as inhibitors of adenylate and guanylate cyclases to reveal their effects on platelets and establish whether they are mediated by PKA/PKG. The commonly used PKA inhibitor H89 inhibited both PKA and PKG but PKA-independently inhibited thrombin-induced platelet activation. In our experiments, KT5720 did not inhibit PKA and had no effect on platelet activation. PKI inhibited PKA activity in platelets but also strongly PKA-independently activated platelets. Inhibition of adenylate and guanylate cyclases may be an alternative approach to analyze PKA/PKG function. Based on our previous and presented data, we conclude that all results where the mentioned PKA inhibitors were used for the analysis of PKA activity in intact platelets should be considered with caution. |
Databáze: | OpenAIRE |
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