Thromb Haemost 2007; 98(05): 1063-1071
DOI: 10.1160/TH07-03-0213
Platelets and Blood Cells
Schattauer GmbH

Leptin signalling and leptin-mediated activation of human platelets: Importance of JAK2 and the phospholipases Cγ2 and A2

Claudia Dellas
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
,
Katrin Schäfer
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
,
Ilonka K. Rohm
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
,
Mareike Lankeit
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
,
Maren Leifheit
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
,
David J. Loskutoff*
2   Department of Cell Biology, Division of Vascular Biology, The Scripps Research Institute, La Jolla, California, USA
,
Gerd Hasenfuss
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
,
Stavros V. Konstantinides
1   Department of Cardiology and Pulmonary Medicine, Georg August University School of Medicine, Goettingen, Germany
› Author Affiliations
Further Information

Publication History

Received 22 March 2007

Accepted after resubmission 01 August 2007

Publication Date:
15 December 2017 (online)

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Summary

Leptin enhances agonist-induced platelet aggregation, and human platelets have been reported to express the leptin receptor. However, the pathways and mediators lying downstream of leptin binding to platelets remain, with few exceptions, unknown. In the present study, we sought to gain further insight into the possible role of leptin as a platelet agonist. Stimulation of platelets with leptin promoted thromboxane generation and activation of αIIbβ3, as demonstrated by PAC-1 binding. Furthermore, it increased the adhesion to immobilised fibrinogen (p<0.001) and induced cytoskeletal rearrangement of both platelets and Meg01 cells. Leptin time- and dose-dependently phosphorylated the intracellular signalling molecules JAK2 and STAT3, although the importance of STAT3 for leptin-induced platelet activation remains to be determined. Important intracellular mediators and pathways activated by leptin downstream of JAK2 were found to include phosphatidylinositol-3 kinase, phospholipase Cγ2 and protein kinase C, as well as the p38 MAP kinase-phospholipase A2 axis. Accordingly, incubation with the specific inhibitors AG490, Ly294002, U73122, and SB203580 prevented leptin-mediated platelet activation. These results help delineate biologically relevant leptin signalling pathways in platelets and may improve our understanding of the mechanisms linking hyperleptinaemia to the increased thrombosis risk in human obesity.

* current address: Torrey Pines Institute for Molecular Studies, San Diego, California, USA