Zhan H, Ma Y, Lin C H S, Kaushansky K
Division of Hematology-Oncology, Department of Medicine, Northport VA Medical Center, Northport, NY, USA.
Department of Medicine, Division of Hematology-Oncology, Stony Brook University, Stony Brook, NY, USA.
Leukemia. 2016 Dec;30(12):2332-2341. doi: 10.1038/leu.2016.114. Epub 2016 May 2.
The myeloproliferative neoplasms (MPNs) are characterized by hematopoietic stem/progenitor cell (HSPC) expansion and overproduction of mature blood cells. The JAK2 mutation is present in hematopoietic cells in a majority of patients with MPNs, but the mechanism(s) responsible for MPN stem cell expansion remain incomplete. One hallmark feature of the marrow in patients with MPNs is megakaryocyte (MK) hyperplasia. We report here that mice bearing a human JAK2 gene restricted exclusively to the MK lineage develop many of the features of a MPN. Specifically, these mice exhibit thrombocytosis, splenomegaly, increased numbers of marrow and splenic hematopoietic progenitors and a substantial expansion of HSPCs. In addition, wild-type mice transplanted with cells from JAK2-bearing MK marrow develop a myeloproliferative syndrome with thrombocytosis and erythrocytosis as well as pan-hematopoietic progenitor and stem cell expansion. As marrow histology in this murine model of myeloproliferation reveals a preferentially perivascular localization of JAK2-mutant MKs and an increased marrow sinusoid vascular density, it adds to accumulating data that MKs are an important component of the marrow HSPC niche, and that MK expansion might indirectly contribute to the critical role of the thrombopoietin/c-Mpl signaling pathway in HSPC maintenance and expansion.
骨髓增殖性肿瘤(MPN)的特征是造血干/祖细胞(HSPC)扩增以及成熟血细胞的过度生成。大多数MPN患者的造血细胞中存在JAK2突变,但导致MPN干细胞扩增的机制仍不完全清楚。MPN患者骨髓的一个标志性特征是巨核细胞(MK)增生。我们在此报告,携带仅在MK谱系中表达的人类JAK2基因的小鼠出现了许多MPN的特征。具体而言,这些小鼠表现出血小板增多、脾肿大、骨髓和脾造血祖细胞数量增加以及HSPC大量扩增。此外,用来自携带JAK2的MK骨髓的细胞移植的野生型小鼠会发展出一种骨髓增殖综合征,伴有血小板增多和红细胞增多以及全造血祖细胞和干细胞扩增。由于这种骨髓增殖小鼠模型的骨髓组织学显示JAK2突变的MK优先定位于血管周围且骨髓窦状血管密度增加,这进一步证明了MK是骨髓HSPC微环境的重要组成部分,并且MK扩增可能间接有助于血小板生成素/c-Mpl信号通路在HSPC维持和扩增中的关键作用。