Transient exposure to miR‐203 enhances the differentiation capacity of established pluripotent stem cells
Autor: | Fatima Valdes-Mora, Elisabet Zapatero-Solana, Juan Carlos Izpisúa-Belmonte, Marta Gómez de Cedrón, Mónica Álvarez-Fernández, Maria J. Bueno, Marianna Trakala, Maria A. Blasco, María Abad, José Fernández-Piqueras, Susan J. Clark, Sagrario Ortega, Marcos Malumbres, Osvaldo Graña-Castro, María Salazar-Roa, Manuel Serrano, Cuiqing Zhong, Tim J Peters, Jaime Muñoz, Rosa Serrano, Yang Yu, Da-Zhi Wang |
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Rok vydání: | 2020 |
Předmět: |
Methyltransferase
Induced Pluripotent Stem Cells Biology Regenerative medicine General Biochemistry Genetics and Molecular Biology Cell Line DNA Methyltransferase 3A Epigenesis Genetic Mice 03 medical and health sciences 0302 clinical medicine microRNA Animals Humans DNA (Cytosine-5-)-Methyltransferases Epigenetics Induced pluripotent stem cell Molecular Biology 030304 developmental biology 0303 health sciences General Immunology and Microbiology Tetraploid complementation assay General Neuroscience Cell Differentiation Articles DNA Methylation Cell biology MicroRNAs DNA methylation Stem cell 030217 neurology & neurosurgery |
Zdroj: | EMBO J |
ISSN: | 1460-2075 0261-4189 |
Popis: | Full differentiation potential along with self‐renewal capacity is a major property of pluripotent stem cells (PSCs). However, the differentiation capacity frequently decreases during expansion of PSCs in vitro. We show here that transient exposure to a single microRNA, expressed at early stages during normal development, improves the differentiation capacity of already‐established murine and human PSCs. Short exposure to miR‐203 in PSCs (miPSCs) induces a transient expression of 2C markers that later results in expanded differentiation potency to multiple lineages, as well as improved efficiency in tetraploid complementation and human–mouse interspecies chimerism assays. Mechanistically, these effects are at least partially mediated by direct repression of de novo DNA methyltransferases Dnmt3a and Dnmt3b, leading to transient and reversible erasure of DNA methylation. These data support the use of transient exposure to miR‐203 as a versatile method to reset the epigenetic memory in PSCs, and improve their effectiveness in regenerative medicine. |
Databáze: | OpenAIRE |
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