miRNome Profiling of Purified Endoderm and Mesoderm Differentiated from hESCs Reveals Functions of miR-483-3p and miR-1263 for Cell-Fate Decisions

被引:24
作者
Ishikawa, Daichi [1 ,2 ]
Diekmann, Ulf [1 ]
Fiedler, Jan [3 ]
Just, Annette [3 ]
Thum, Thomas [3 ,4 ]
Lenzen, Sigurd [1 ]
Naujok, Ortwin [1 ]
机构
[1] Hannover Med Sch, Inst Clin Biochem, Carl Neuberg Str 1, D-30625 Hannover, Germany
[2] Tokushima Univ, Dept Surg, 3-18-15 Kuramoto, Tokushima 7708503, Japan
[3] Hannover Med Sch, IMTTS, Carl Neuberg Str 1, D-30625 Hannover, Germany
[4] Imperial Coll London, Natl Heart & Lung Inst, Sydney St, London SW3 6NP, England
来源
STEM CELL REPORTS | 2017年 / 9卷 / 05期
关键词
EMBRYONIC STEM-CELLS; DEFINITIVE ENDODERM; PANCREATIC ENDODERM; MICRORNAS; PLURIPOTENCY; EXPRESSION; SIGNATURE; SUBTYPES; PATTERN; TARGETS;
D O I
10.1016/j.stemcr.2017.10.011
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Pluripotent stem cells hold great promise for regenerative medicine since they can differentiate into all somatic cells. MicroRNAs (miRNAs) could be important for the regulation of these cell-fate decisions. Profiling of miRNAs revealed 19 differentially expressed miRNAs in the endoderm and 29 in the mesoderm when analyzing FACS-purified cells derived from human embryonic stem cells. The mesodermal-enriched miR-483-3p was identified as an important regulator for the generation of mesodermal PDGFRA(+) paraxial cells. Repression of its target PGAM1 significantly increased the number of PDGFRA(+) cells. Furthermore, miR-483-3p, miR-199a-3p, and miR-214-3p might also have functions for the mesodermal progenitors. The endoderm-specific miR-489-3p and miR-1263 accelerated and increased endoderm differentiation upon overexpression. KLF4 was identified as a target of miR-1263. RNAi-mediated downregulation of KLF4 partially mimicked miR-1263 overexpression. Thus, the effects of this miRNA were mediated by facilitating differentiation through destabilization of pluripotency along with other not yet defined targets.
引用
收藏
页码:1588 / 1603
页数:16
相关论文
共 40 条
[1]   The Nodal inhibitor Lefty is negatively modulated by the microRNA miR-302 in human embryonic stem cells [J].
Barroso-delJesus, Alicia ;
Lucena-Aguilar, Gema ;
Sanchez, Laura ;
Ligero, Gertrudis ;
Gutierrez-Aranda, Ivan ;
Menendez, Pablo .
FASEB JOURNAL, 2011, 25 (05) :1497-1508
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   Dicer is essential for mouse development [J].
Bernstein, E ;
Kim, SY ;
Carmell, MA ;
Murchison, EP ;
Alcorn, H ;
Li, MZ ;
Mills, AA ;
Elledge, SJ ;
Anderson, KV ;
Hannon, GJ .
NATURE GENETICS, 2003, 35 (03) :215-217
[4]   Defining embryonic stem cell identity using differentiation-related microRNAs and their potential targets [J].
Chen, Caifu ;
Ridzon, Dana ;
Lee, Chung-Tien ;
Blake, Julie ;
Sun, Yongming ;
Strauss, William M. .
MAMMALIAN GENOME, 2007, 18 (05) :316-327
[5]  
D'haene Barbara, 2012, Methods Mol Biol, V822, P261, DOI 10.1007/978-1-61779-427-8_18
[6]   Anterior-Posterior Patterning of Definitive Endoderm Generated from Human Embryonic Stem Cells Depends on the Differential Signaling of Retinoic Acid, Wnt-, and BMP-Signaling [J].
Davenport, Claudia ;
Diekmann, Ulf ;
Budde, Insa ;
Detering, Nora ;
Naujok, Ortwin .
STEM CELLS, 2016, 34 (11) :2635-2647
[7]  
Diekmann U, 2016, METHODS MOL BIOL, V1341, P157, DOI 10.1007/7651_2015_220
[8]   A Reliable and Efficient Protocol for Human Pluripotent Stem Cell Differentiation into the Definitive Endoderm Based on Dispersed Single Cells [J].
Diekmann, Ulf ;
Lenzen, Sigurd ;
Naujok, Ortwin .
STEM CELLS AND DEVELOPMENT, 2015, 24 (02) :190-204
[9]   MicroRNA Target Sites as Genetic Tools to Enhance Promoter-Reporter Specificity for the Purification of Pancreatic Progenitor Cells from Differentiated Embryonic Stem Cells [J].
Diekmann, Ulf ;
Elsner, Matthias ;
Fiedler, Jan ;
Thum, Thomas ;
Lenzen, Sigurd ;
Naujok, Ortwin .
STEM CELL REVIEWS AND REPORTS, 2013, 9 (05) :555-568
[10]   INVITED REVIEW Role of non-coding RNAs in pancreatic beta-cell development and physiology [J].
Eliasson, L. ;
Esguerra, J. L. S. .
ACTA PHYSIOLOGICA, 2014, 211 (02) :273-284