MicroRNA-200c-141 and ΔNp63 are required for breast epithelial differentiation and branching morphogenesis

被引:20
|
作者
Hilmarsdottir, Bylgja [1 ,2 ]
Briem, Eirikur [1 ,2 ]
Sigurdsson, Valgardur [1 ]
Franzdottir, Sigridur Rut [1 ]
Ringner, Markus [4 ]
Arason, Ari Jon [1 ,2 ]
Bergthorsson, Jon Thor [1 ,2 ]
Magnusson, Magnus Karl [1 ,2 ,3 ]
Gudjonsson, Thorarinn [1 ,2 ]
机构
[1] Univ Iceland, Sch Hlth Sci, Fac Med, Stem Cell Res Unit,Biomed Ctr,Dept Anat, IS-101 Reykjavik, Iceland
[2] Landspitali Univ Hosp, Dept Lab Hematol, Reykjavik, Iceland
[3] Univ Iceland, Sch Hlth Sci, Fac Med, Dept Med Pharmacol & Toxicol, IS-101 Reykjavik, Iceland
[4] Lund Univ, Dept Clin Sci Lund, Div Oncol & Pathol, S-22100 Lund, Sweden
关键词
MiR-200c-141; Delta Np63; Breast cancer; Breast morphogenesis; Stem cells; EMT; STEM-CELLS; MESENCHYMAL TRANSITION; P63; CANCER; MIR-200; EXPRESSION; BIOLOGY; FAMILY; TARGET; GENES;
D O I
10.1016/j.ydbio.2015.05.007
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The epithelial compartment of the breast contains two lineages, the luminal- and the myoepithelial cells. D492 is a breast epithelial cell line with stem cell properties that forms branching epithelial structures in 3D culture with both luminal- and myoepithelial differentiation. We have recently shown that D492 undergo epithelial to mesenchymal transition (EMT) when co-cultured with endothelial cells. This 3D co-culture model allows critical analysis of breast epithelial lineage development and EMT. In this study, we compared the microRNA (miR) expression profiles for D492 and its mesenchymal-derivative D492M. Suppression of the miR-200 family in D492M was among the most profound changes observed. Exogenous expression of miR-200c-141 in D492M reversed the EMT phenotype resulting in gain of luminal but not myoepithelial differentiation. In contrast, forced expression of Delta Np63 in D492M restored the myoepithelial phenotype only. Co-expression of miR-200c-141 and Delta Np63 in D492M restored the branching morphogenesis in 3D culture underlining the requirement for both luminal and myoepithelial elements for obtaining full branching morphogenesis in breast epithelium. Introduction of a miR-200c-141 construct in both D492 and D492M resulted in resistance to endothelial induced EMT. In conclusion, our data suggests that expression of miR-200c-141 and Delta Np63 in D492M can reverse EMT resulting in luminal- and myoepithelial differentiation, respectively, demonstrating the importance of these molecules in epithelial integrity in the human breast. (C) 2015 The Authors. Published by Elsevier Inc.
引用
收藏
页码:150 / 161
页数:12
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