Journal of Thrombosis and Haemostasis 2014-10-01

Multiplexed phosphospecific flow cytometry enables large-scale signaling profiling and drug screening in blood platelets.

B E J Spurgeon, A Aburima, N G Oberprieler, K Taskén, K M Naseem

文献索引:J. Thromb. Haemost. 12(10) , 1733-43, (2014)

全文:HTML全文

摘要

Dissecting the signaling events that contribute to platelet activation will increase our understanding of platelet function and aid in the development of new antiplatelet agents. However, high-throughput methodology for the quantitative analysis of platelet signaling events is still lacking.To develop a high-throughput assay for the analysis of platelet signaling events in whole blood.We developed a fluorescent barcoding protocol to facilitate multiplexing and enable large-scale signaling profiling in platelets in whole blood. The methodology allowed simultaneous staining and acquisition of 24-96 samples in a single analysis tube with a standard flow cytometer. This approach significantly reduced experimental numbers, data acquisition time, and antibody consumption, while providing automated statistically rich quantitative data on signaling events. Using vasodilator-stimulated phosphoprotein (VASP), an established marker of platelet inhibition and antiplatelet drug therapy, we demonstrated that the assay could detect subtle changes in phosphoVASP-Ser157/239 in response to cAMP-elevating agents of varying potency and known modulators of the cAMP signaling cascade. The assay could be used with washed platelets or whole blood, analyzed immediately or frozen, without any significant change in assay performance. To demonstrate the usefulness of the assay as a drug discovery platform, we examined a prostaglandin screening library. Our screen of 70 prostaglandin derivatives revealed three previously uncharacterized lipids that stimulated phosphorylation of VASP-Ser157. Follow-up analyses demonstrated that these agents elevated intraplatelet cAMP and inhibited collagen-induced platelet aggregation.This novel method enables rapid, large-scale quantitative signaling profiling and compound screening in human platelets present in whole blood.© 2014 International Society on Thrombosis and Haemostasis.


相关化合物

  • S-亚硝基谷胱甘肽
  • 腺苷3',5'-环单磷酸...
  • 列腺素 E1
  • 1H-[1,2,4]恶二唑并...
  • 前列腺素 D2
  • 环磷酸腺苷
  • 3-异丁基-1-甲基黄...
  • 米力农
  • 3-[(2-环己基-2-羟...

相关文献:

Down regulation of NO signaling in Trypanosoma cruzi upon parasite-extracellular matrix interaction: changes in protein modification by nitrosylation and nitration.

2015-04-01

[PLoS Negl. Trop. Dis. 9 , e0003683, (2015)]

Lipopolysaccharides Promote S-Nitrosylation and Proteasomal Degradation of Liver Kinase B1 (LKB1) in Macrophages in Vivo.

2015-07-31

[J. Biol. Chem. 290 , 19011-7, (2015)]

S-nitrosylation triggers ABI5 degradation to promote seed germination and seedling growth.

2015-01-01

[Nat. Commun. 6 , 8669, (2015)]

Comparison of S-nitrosoglutathione- and staurosporine-induced apoptosis in human neural cells.

2014-12-01

[Can. J. Physiol. Pharmacol. 92(12) , 1001-11, (2014)]

S-nitrosation of mitochondrial connexin 43 regulates mitochondrial function.

2014-01-01

[Basic Res. Cardiol. 109(5) , 433, (2014)]

更多文献...