| Literature DB >> 28887433 |
Sebastian Drube1, Randy Grimlowski2, Carsten Deppermann3, Julia Fröbel4, Florian Kraft2, Nico Andreas2, David Stegner3, Jan Dudeck4, Franziska Weber2, Mandy Rödiger2, Christiane Göpfert2, Julia Drube5, Daniela Reich5, Bernhard Nieswandt3, Anne Dudeck4, Thomas Kamradt2.
Abstract
The neurobeachin-like 2 protein (Nbeal2) belongs to the family of beige and Chediak-Higashi (BEACH) domain proteins. Loss-of-function mutations in the human NBEAL2 gene or Nbeal2 deficiency in mice cause gray platelet syndrome, a bleeding disorder characterized by macrothrombocytopenia, splenomegaly, and paucity of α-granules in megakaryocytes and platelets. We found that in mast cells, Nbeal2 regulates the activation of the Shp1-STAT5 signaling axis and the composition of the c-Kit/STAT signalosome. Furthermore, Nbeal2 mediates granule formation and restricts the expression of the transcription factors, IRF8, GATA2, and MITF as well as of the cell-cycle inhibitor p27, which are essential for mast cell differentiation, proliferation, and cytokine production. These data demonstrate the relevance of Nbeal2 in mast cells above and beyond granule biosynthesis.Entities:
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Year: 2017 PMID: 28887433 DOI: 10.4049/jimmunol.1700556
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422