Battinelli Elisabeth M, Hartwig John H, Italiano Joseph E
Translational Medicine Division, Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts 02115, USA.
Curr Opin Hematol. 2007 Sep;14(5):419-26. doi: 10.1097/MOH.0b013e3282bad151.
The aim of this review is to explore the state of the art knowledge on the cell biological and molecular pathways that regulate megakaryopoiesis and lead to platelet production.
In the last 2 years there has been considerable progress in the elucidation of molecular mechanisms of megakaryocyte development and platelet biogenesis, driven by the application of modern molecular biology approaches to these specialized and unique cells. Studies have for the first time visualized endomitotic spindle dynamics, characterized the maturation of the demarcation membrane system, and delineated the mechanics of organelle transport and microtubule assembly in living megakaryocytes. The role of specific molecules in platelet production has been elucidated in greater detail by combining molecular studies with genetically engineered mice as well as embryonic cell culture systems.
This review integrates the latest studies of megakaryocyte development into the molecular pathways that regulate megakaryopoiesis and thrombopoiesis. Decoding the pathways of megakaryopoiesis and platelet production should help revolutionize the management of thrombocytopenia and other platelet disorders.
本综述旨在探讨调控巨核细胞生成并导致血小板产生的细胞生物学和分子途径的最新知识状况。
在过去两年中,通过将现代分子生物学方法应用于这些特殊且独特的细胞,巨核细胞发育和血小板生物发生的分子机制阐释取得了显著进展。研究首次可视化了核内有丝分裂纺锤体动力学,表征了分界膜系统的成熟过程,并描绘了活巨核细胞中细胞器运输和微管组装的机制。通过将分子研究与基因工程小鼠以及胚胎细胞培养系统相结合,特定分子在血小板产生中的作用得到了更详细的阐明。
本综述将巨核细胞发育的最新研究整合到调控巨核细胞生成和血小板生成的分子途径中。解码巨核细胞生成和血小板产生的途径应有助于彻底改变血小板减少症和其他血小板疾病的管理。