Drube Sebastian, Grimlowski Randy, Deppermann Carsten, Fröbel Julia, Kraft Florian, Andreas Nico, Stegner David, Dudeck Jan, Weber Franziska, Rödiger Mandy, Göpfert Christiane, Drube Julia, Reich Daniela, Nieswandt Bernhard, Dudeck Anne, Kamradt Thomas
Institute of Immunology, Jena University Hospital, 07743 Jena, Germany;
Institute of Immunology, Jena University Hospital, 07743 Jena, Germany.
J Immunol. 2017 Oct 15;199(8):2948-2957. doi: 10.4049/jimmunol.1700556. Epub 2017 Sep 8.
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 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.
类神经beachin样蛋白2(Nbeal2)属于米色和切-东综合征(BEACH)结构域蛋白家族。人类基因中的功能丧失突变或小鼠中的Nbeal2缺陷会导致灰色血小板综合征,这是一种出血性疾病,其特征为大血小板减少、脾肿大以及巨核细胞和血小板中α颗粒缺乏。我们发现,在肥大细胞中,Nbeal2调节Shp1-STAT5信号轴的激活以及c-Kit/STAT信号小体的组成。此外,Nbeal2介导颗粒形成,并限制转录因子IRF8、GATA2和MITF以及细胞周期抑制剂p27的表达,这些对于肥大细胞的分化、增殖和细胞因子产生至关重要。这些数据证明了Nbeal2在肥大细胞中除颗粒生物合成之外的相关性。