血小板生成素
巨核细胞生成
骨髓
生物
细胞生物学
细胞周期
巨核细胞
细胞分裂
原癌基因酪氨酸蛋白激酶Src
细胞
细胞生长
癌症研究
激酶
免疫学
干细胞
造血
遗传学
作者
Brian J. Lannutti,Noel Blake,Manish J. Gandhi,Jo Anna Reems,Jonathan G. Drachman
出处
期刊:Blood
[American Society of Hematology]
日期:2005-01-28
卷期号:105 (10): 3875-3878
被引量:57
标识
DOI:10.1182/blood-2004-10-3934
摘要
Abstract Megakaryocytes (MKs) undergo successive rounds of endomitosis during differentiation, resulting in polyploidy (typically, 16-64N). Previous studies have demonstrated that this occurs through an interruption of normal cell cycle progression during anaphase. However, the molecular mechanism(s) controlling this unique process is undefined. In the present report, we examine the effect of an Src kinase inhibitor, SU6656, on thrombopoietin (TPO)-induced growth and differentiation. Remarkably, when SU6656 (2.5 μM) was added to a megakaryocytic cell line, UT-7/TPO, the cells ceased cell division but continued to accumulate DNA by endomitosis. During this interval, CD41 and CD61 expression on the cell surface increased. Similar effects on polyploidization and MK differentiation were seen with expanded primary MKs, bone marrow from 2 patients with myelodysplastic syndrome, and other cell lines with MK potential. Our data suggest that SU6656 might be useful as a differentiation-inducing agent for MKs and is an important tool for understanding the molecular basis of MK endomitosis.
科研通智能强力驱动
Strongly Powered by AbleSci AI