Deutsch Varda, Katz Ben Zion, Tomer Aaron
The Hematology Institute, Tel Aviv Medical Center, Tel Aviv.
Harefuah. 2010 May;149(5):291-7, 336.
Megakaryocytopoiesis involves the commitment of hematopoietic stem cell, the proliferation and terminal differentiation of the megakaryocytic progenitors and maturation to platelet producing megakaryocytes (MK). MKs align adjacent to bone marrow vascular endothelial cells, and form proplatelets. Platelets are released, or sheared from the MK directly into the circulation from the tips of proplatelets which protrude into the vascular lumen. The regulation of megakaryocytopoiesis is mediated through multiple hematopoietic growth factors, chemokines and cellular interactions via signal transduction pathways and integrated transcription factors. The primary physiological growth factor that regulates megakaryocytopoiesis and platelet production is thrombopoietin. Circulating Levels of thrombopoietin (TPO) induce concentration-dependent proliferation and maturation of MK progenitors by binding to the c-Mpl receptor and signaling induction. Increased concentration of free TPO resulting from decreased platelet turnover rates enables the compensatory response of marrow MKs to drive amplified platelet production. C-MpL signaling is orchestrated by a complex cascade of signaling molecules inducing the action of specific transcription factors to drive MK proliferation and maturation. Newly developed thrombopoietic agents operating via c-Mpl receptor have now been proven useful in supporting platelet production in thrombocytopenic states. In this article, the authors review the regulation of megakaryocytopoiesis and platelet production in normal and disease states, and new approaches of thrombopoietic therapy.
巨核细胞生成涉及造血干细胞的定向分化、巨核细胞祖细胞的增殖和终末分化以及向产生血小板的巨核细胞(MK)的成熟过程。巨核细胞排列在骨髓血管内皮细胞附近,并形成前血小板。血小板从前血小板的末端释放出来,或者直接从巨核细胞上剪切下来进入循环,前血小板的末端伸入血管腔。巨核细胞生成的调节是通过多种造血生长因子、趋化因子以及经由信号转导途径和整合转录因子的细胞间相互作用介导的。调节巨核细胞生成和血小板产生的主要生理生长因子是血小板生成素。血小板生成素(TPO)的循环水平通过与c-Mpl受体结合并诱导信号传导,从而诱导巨核细胞祖细胞进行浓度依赖性增殖和成熟。血小板周转率降低导致游离TPO浓度升高,从而使骨髓巨核细胞产生代偿性反应,以驱动血小板生成增加。C-MpL信号传导由一系列复杂的信号分子精心编排,这些信号分子诱导特定转录因子的作用,以驱动巨核细胞的增殖和成熟。现已证明,通过c-Mpl受体发挥作用的新型血小板生成剂在支持血小板减少症状态下的血小板生成方面是有用的。在本文中,作者综述了正常和疾病状态下巨核细胞生成和血小板产生的调节以及血小板生成治疗的新方法。