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The Ashwell-Morell receptor regulates hepatic thrombopoietin production via JAK2-STAT3 signaling.

Renata GrozovskyAntonija Jurak BegonjaKaifeng LiuGary VisnerJohn H HartwigHervé FaletKarin M Hoffmeister
Published in: Nature medicine (2014)
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.
Keyphrases
  • binding protein
  • poor prognosis
  • recombinant human
  • transcription factor
  • long non coding rna
  • red blood cell
  • nuclear factor
  • small molecule
  • immune response
  • amino acid
  • toll like receptor
  • dna binding