Division of Hematology, The Children's Hospital of Philadelphia, Philadelphia, PA, USA.
Blood. 2010 Dec 2;116(23):e128-38. doi: 10.1182/blood-2010-06-292920. Epub 2010 Aug 18.
MicroRNAs are small noncoding RNAs that regulate cellular development by interfering with mRNA stability and translation. We examined global microRNA expression during the differentiation of murine hematopoietic progenitors into megakaryocytes. Of 435 miRNAs analyzed, 13 were up-regulated and 81 were down-regulated. Many of these changes are consistent with miRNA profiling studies of human megakaryocytes and platelets, although new patterns also emerged. Among 7 conserved miRNAs that were up-regulated most strongly in murine megakaryocytes, 6 were also induced in the related erythroid lineage. MiR-146a was strongly up-regulated during mouse and human megakaryopoiesis but not erythropoiesis. However, overexpression of miR-146a in mouse bone marrow hematopoietic progenitor populations produced no detectable alterations in megakaryocyte development or platelet production in vivo or in colony assays. Our findings extend the repertoire of differentially regulated miRNAs during murine megakaryopoiesis and provide a useful new dataset for hematopoiesis research. In addition, we show that enforced hematopoietic expression of miR-146a has minimal effects on megakaryopoiesis. These results are compatible with prior studies indicating that miR-146a inhibits megakaryocyte production indirectly by suppressing inflammatory cytokine production from innate immune cells, but cast doubt on a different study, which suggests that this miRNA inhibits megakaryopoiesis cell-autonomously.
miRNAs 是一类小的非编码 RNA,可以通过干扰 mRNA 的稳定性和翻译来调节细胞的发育。我们研究了小鼠造血祖细胞向巨核细胞分化过程中的全局 miRNA 表达。在分析的 435 个 miRNA 中,有 13 个上调,81 个下调。这些变化中有许多与人类巨核细胞和血小板的 miRNA 分析研究一致,但也出现了新的模式。在小鼠巨核细胞中上调最明显的 7 个保守 miRNA 中,有 6 个在相关的红细胞谱系中也被诱导。miR-146a 在小鼠和人类巨核细胞发生过程中强烈上调,但在红细胞发生过程中没有上调。然而,在小鼠骨髓造血祖细胞群体中过表达 miR-146a,在体内或集落测定中并没有检测到巨核细胞发育或血小板生成的明显改变。我们的发现扩展了小鼠巨核细胞发生过程中差异调节的 miRNA 谱,并为造血研究提供了一个有用的新数据集。此外,我们表明 miR-146a 在造血系统中的强制表达对巨核细胞发生的影响很小。这些结果与先前的研究一致,表明 miR-146a 通过抑制先天免疫细胞中炎症细胞因子的产生间接抑制巨核细胞的产生,但与另一项研究相矛盾,该研究表明该 miRNA 自主抑制巨核细胞发生。