Suppr超能文献

原发性骨髓纤维化和特发性血小板增多症巨核细胞的 microRNA 表达谱分析。

MicroRNA expression profiling of megakaryocytes in primary myelofibrosis and essential thrombocythemia.

机构信息

Institute of Pathology, 30625, Hannover, Germany.

出版信息

Platelets. 2009 Sep;20(6):391-400. doi: 10.1080/09537100903114537.

Abstract

In primary myelofibrosis (PMF) and essential thrombocythemia (ET) the megakaryocytic lineage characteristically shows aberrant proliferation and maturation in which the regulatory microRNA (miR) system might be involved. Laser-microdissected PMF and ET megakaryocytes were analysed with real-time polymerase chain reaction (PCR) low density arrays comprising 365 microRNAs. The highest megakaryocytic expression levels were observed for miR-223, which is known to be expressed also in granulopoiesis. Cluster analysis revealed a tendency of disease-specific megakaryocytic microRNA expression profiles indicating that a complex shift of microRNA expression appears to be the underlying defect. Increased accumulation of miR-146b was observed in cellular stage PMF (p = 0.0125) but not ET megakaryopoiesis. In conclusion, this is the first microRNA profiling of in situ-derived PMF, ET and normal megakaryocytes.

摘要

在原发性骨髓纤维化(PMF)和特发性血小板增多症(ET)中,巨核细胞谱系表现出异常增殖和成熟,其中调节 microRNA(miR)系统可能参与其中。使用包含 365 种 microRNAs 的实时聚合酶链反应(PCR)低密度阵列分析了激光微切割的 PMF 和 ET 巨核细胞。miR-223 的巨核细胞表达水平最高,已知其在粒细胞生成中也有表达。聚类分析显示出疾病特异性巨核细胞 microRNA 表达谱的趋势,表明 microRNA 表达的复杂转移似乎是潜在的缺陷。在细胞阶段 PMF 中观察到 miR-146b 的积累增加(p=0.0125),但 ET 巨核细胞生成中没有增加。总之,这是对原位衍生的 PMF、ET 和正常巨核细胞进行的首次 microRNA 分析。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验