Abstract

CD40 ligand (CD40L), a member of the tumor necrosis factor (TNF) superfamily, binds to CD40, leading to many effects depending on target cell type. Platelets express CD40L and are a major source of soluble CD40L. CD40L has been shown to potentiate platelet activation and thrombus formation, involving both CD40-dependent and -independent mechanisms. A family of proteins called TNF receptor associated factors (TRAFs) plays key roles in mediating CD40L-CD40 signaling. Platelets express several TRAFs. It has been shown that TRAF2 plays a role in CD40L-mediated platelet activation. Here we show that platelet also express TRAF3, which plays a negative role in regulating platelet activation. Thrombin- or collagen-induced platelet aggregation and secretion are increased in TRAF3 knockout mice. The expression levels of collagen receptor GPVI and integrin αIIbβ3 in platelets were not affected by deletion of TRAF3, suggesting that increased platelet activation in the TRAF3 knockout mice was not due to increased expression platelet receptors. Time to formation of thrombi in a FeCl3-induced thrombosis model was significantly shortened in the TRAF3 knockout mice. However, mouse tail-bleeding times were not affected by deletion of TRAF3. Thus, TRAF3 plays a negative role in platelet activation and in thrombus formation in vivo.

Document Type

Article

Publication Date

12-7-2017

Notes/Citation Information

Published in Scientific Reports, v. 7, article no. 17112, p. 1-11.

© The Author(s) 2017

This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Digital Object Identifier (DOI)

https://doi.org/10.1038/s41598-017-17189-1

Funding Information

This work is supported by the American Society of Hematology (ASH) Bridge Grant Award (to Z.L.), NIH, NHLBI, Grant HL123927 (to Z.L.), the American Heart Association (AHA) Great Rivers Affiliate Grand-in-aid (to Z. L.), NIH, NCI, Grant CA158402 (to P.X.), NIH, NHLBI, Grant HL113640 (to X.A.), and the AHA Great Rivers Affiliate Scientist Development Grant (to B.X.). R.Z. is supported by the China Scholarship Council.

Related Content

Supplementary information accompanies this paper at https://doi.org/10.1038/s41598-017-17189-1.

41598_2017_17189_MOESM1_ESM.pdf (909 kB)
Supplementary data

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