Hoffman R, Briddell R, Bruno E
Department of Medicine, Indiana University School of Medicine, Indianapolis.
Yale J Biol Med. 1990 Sep-Oct;63(5):411-8.
At least two classes of human megakaryocyte progenitor cells have been identified: the burst-forming unit megakaryocyte (BFU-MK) and the colony-forming unit megakaryocyte (CFU-MK). The BFU-MK is the most primitive progenitor cell committed to the megakaryocytic lineage. The CFU-MK appears to be a more differentiated megakaryocyte progenitor cell and is thought to be ultimately a descendant of the BFU-MK. A number of recombinant cytokines have recently been shown to be able to promote megakaryocyte colony formation in vitro. Recombinant GM-CSF and IL-3, in particular, have the ability to promote both CFU-MK- and BFU-MK-derived colony stimulatory formation. The activities of these two cytokines on in vitro megakaryocytopoiesis are also additive. Recent results of clinical trials in both primates and humans, in which these glycoproteins were administered in vivo, suggest that these cytokines, both alone and in combination, can enhance in vivo thrombopoiesis and therefore may be potentially useful in the treatment of thrombocytopenic disorders.
爆式巨核细胞集落形成单位(BFU-MK)和巨核细胞集落形成单位(CFU-MK)。BFU-MK是最原始的致力于巨核细胞系的祖细胞。CFU-MK似乎是一种更分化的巨核细胞祖细胞,被认为最终是BFU-MK的后代。最近有许多重组细胞因子已被证明能够在体外促进巨核细胞集落形成。特别是重组粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素-3(IL-3),具有促进CFU-MK和BFU-MK来源的集落刺激形成的能力。这两种细胞因子对体外巨核细胞生成的活性也是相加的。在灵长类动物和人类中进行的临床试验的最新结果表明,在体内施用这些糖蛋白时,这些细胞因子单独或联合使用都可以增强体内血小板生成,因此可能在治疗血小板减少症中具有潜在用途。