Robert Amélie, Cortin Valérie, Garnier Alain, Pineault Nicolas
Département de Recherche et Développement, Héma-Québec, Québec City, QC, Canada.
Methods Mol Biol. 2012;788:219-47. doi: 10.1007/978-1-61779-307-3_16.
The cloning of thrombopoietin together with advances in the culture of hematopoietic stem cells have paved the way for the study of megakaryopoiesis, ongoing clinical trials and, in the future, for the potential therapeutic use of ex vivo produced blood substitutes, such as platelets. This chapter describes a 14-day culture protocol for the production of human megakaryocytes (MKs) and platelets, and assays that can be used to characterize the functional properties of the platelets produced ex vivo. CD34(+) cells isolated from cord blood cells are grown in a serum-free medium supplemented with newly developed cytokine cocktails optimized for MK differentiation, expansion, and maturation. Detailed methodologies for flow cytometry analysis of MKs and platelets, for the purification of platelets and functional assays, are presented together with supporting figures. The chapter also provides a brief review on megakaryocytic differentiation and ex vivo MK cultures.
血小板生成素的克隆以及造血干细胞培养技术的进展,为巨核细胞生成的研究、正在进行的临床试验以及未来体外生产的血液替代品(如血小板)的潜在治疗应用铺平了道路。本章介绍了一种为期14天的培养方案,用于生产人巨核细胞(MKs)和血小板,以及可用于表征体外产生的血小板功能特性的检测方法。从脐血细胞中分离出的CD34(+)细胞在无血清培养基中培养,该培养基添加了针对MK分化、扩增和成熟优化的新开发细胞因子混合物。文中还给出了支持性图表,介绍了MKs和血小板的流式细胞术分析、血小板纯化及功能检测的详细方法。本章还简要回顾了巨核细胞分化和体外MK培养。