Drachman J G, Rojnuckarin P, Kaushansky K
Division of Hematology, University of Washington School of Medicine, Seattle, Washington, 98195, USA.
Methods. 1999 Mar;17(3):238-49. doi: 10.1006/meth.1998.0734.
Thrombopoietin (TPO) and its receptor Mpl support all of the developmental step necessary for megakaryocytopoiesis. In the past few years, the signaling pathways utilized by this member of the cytokine receptor family have been extensively studied, especially JAK/STAT, Ras/MAP kinase, Shc, and other adapter molecules. Many if not most of the secondary signaling pathways activated by thrombopoietin have also been identified upon binding of other hematopoietic growth factors to their cognate receptors, making the study of Mpl signaling representative of the field in general. However, identifying unique molecules or combinations of signals that direct megakaryocyte development has been an elusive goal and has led some investigators to conclude that there is little specificity during Mpl signal transduction. In this article we review the data regarding Mpl signaling with particular attention to the methods employed and critical interpretation of the data generated. Future studies will have to focus on primary bone marrow cells and intact animal models rather than transformed cell lines. Furthermore, it is likely that a comprehensive, integrative analysis of the many pathways activated by ligand binding will be necessary to understand the physiology of cytokine signaling.
血小板生成素(TPO)及其受体Mpl支持巨核细胞生成所需的所有发育步骤。在过去几年中,细胞因子受体家族的这一成员所利用的信号通路已得到广泛研究,尤其是JAK/STAT、Ras/MAP激酶、Shc及其他衔接分子。血小板生成素激活的许多(即便不是大多数)次级信号通路,在其他造血生长因子与其同源受体结合时也已被识别出来,这使得对Mpl信号传导的研究总体上代表了该领域。然而,识别指导巨核细胞发育的独特分子或信号组合一直是一个难以实现的目标,这导致一些研究人员得出结论,Mpl信号转导过程中特异性很小。在本文中,我们回顾了有关Mpl信号传导的数据,特别关注所采用的方法以及对所产生数据的关键解读。未来的研究将不得不聚焦于原代骨髓细胞和完整动物模型,而非转化细胞系。此外,对配体结合激活的众多通路进行全面、综合的分析,可能对于理解细胞因子信号传导的生理学是必要的。