| Literature DB >> 25485912 |
Renata Grozovsky1, Antonija Jurak Begonja1, Kaifeng Liu2, Gary Visner2, John H Hartwig1, Hervé Falet1, Karin M Hoffmeister1.
Abstract
The hepatic Ashwell-Morell receptor (AMR) can bind and remove desialylated platelets. Here we demonstrate that platelets become desialylated as they circulate and age in blood. Binding of desialylated platelets to the AMR induces hepatic expression of thrombopoietin (TPO) mRNA and protein, thereby regulating platelet production. Endocytic AMR controls TPO expression through Janus kinase 2 (JAK2) and the acute phase response signal transducer and activator of transcription 3 (STAT3) in vivo and in vitro. Recognition of this newly identified physiological feedback mechanism illuminates the pathophysiology of platelet diseases, such as essential thrombocythemia and immune thrombocytopenia, and contributes to an understanding of the mechanisms of thrombocytopenia observed with JAK1/2 inhibition.Entities:
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Year: 2014 PMID: 25485912 PMCID: PMC4303234 DOI: 10.1038/nm.3770
Source DB: PubMed Journal: Nat Med ISSN: 1078-8956 Impact factor: 53.440