Program in Developmental Biology, Baylor College of Medicine, Houston, TX 77030, USA.
J Cell Sci. 2010 Feb 15;123(Pt 4):606-18. doi: 10.1242/jcs.056812. Epub 2010 Jan 26.
In an effort to understand the potential role of microRNAs (miRNAs) in mammary-gland stem or progenitor cells, miRNA microarrays were performed on subpopulations of the mouse mammary epithelial cell (MEC) line COMMA-DbetaGeo. This cell line contains a heterogeneous subpopulation of progenitors characterized by the expression of stem cell antigen 1 (Sca-1; encoded by Ly6a). Microarray analysis indicated that the Sca-1 subpopulations have distinct miRNA expression profiles. Functional studies were performed on miR-205, which was highly expressed in the Sca-1-positive (Sca-1(+)) cells. When miR-205 was overexpressed in vitro, the COMMA-DbetaGeo cells underwent several significant morphological and molecular changes. miR-205 overexpression led to an expansion of the progenitor-cell population, decreased cell size and increased cellular proliferation. In addition, the colony-forming potential of the two Sca-1 subpopulations was increased. Target prediction for miR-205 indicated that it might regulate the expression of the tumor-suppressor protein PTEN. Overexpression studies using reporter constructs confirmed that PTEN expression is regulated by miR-205. In addition to PTEN, several other putative and previously validated miR-205 targets were identified by microarray analysis, including the previously reported miR-205 targets ZEB1 and ZEB2. Additionally, in normal mouse MECs, high expression of miR-205 was observed in stem-cell-enriched cell populations isolated by FACS using established cell-surface markers.
为了研究 microRNAs(miRNAs)在乳腺干细胞或祖细胞中的潜在作用,对小鼠乳腺上皮细胞(MEC)系 COMMA-DbetaGeo 的亚群进行了 miRNA 微阵列分析。该细胞系包含一个由干细胞抗原 1(Sca-1;由 Ly6a 编码)表达特征的异质祖细胞亚群。微阵列分析表明,Sca-1 亚群具有不同的 miRNA 表达谱。对 miR-205 进行了功能研究,该 miRNA 在 Sca-1 阳性(Sca-1(+))细胞中高度表达。当 miR-205 在体外过表达时,COMMA-DbetaGeo 细胞经历了几个显著的形态和分子变化。miR-205 的过表达导致祖细胞群体的扩张、细胞体积减小和细胞增殖增加。此外,两个 Sca-1 亚群的集落形成潜力增加。miR-205 的靶预测表明,它可能调节肿瘤抑制蛋白 PTEN 的表达。使用报告基因构建体进行的过表达研究证实,PTEN 的表达受 miR-205 调控。除了 PTEN,通过微阵列分析还鉴定了几个其他推定的和以前验证过的 miR-205 靶标,包括先前报道的 miR-205 靶标 ZEB1 和 ZEB2。此外,在正常的小鼠 MEC 中,使用已建立的细胞表面标记物通过 FACS 分离的富含干细胞的细胞群中观察到 miR-205 的高表达。