MicroRNA characterization in equine induced pluripotent stem cells

Autor: Ximena Garate, Gabriel Neiman, Santiago Gabriel Miriuka, Lucía Natalia Moro, Alejandro La Greca, Ariel Waisman, Guadalupe Amín, Verónica Alejandra Furmento, Carlos Luzzani, Natalia Lucía Santín Velazque, G. Vichera, Gustavo Sevlever
Rok vydání: 2018
Předmět:
0301 basic medicine
Nuclear Transfer Techniques
Embryology
Cellular differentiation
Biochemistry
pluripotent
Animal Cells
Medicine and Health Sciences
Induced pluripotent stem cell
Connective Tissue Cells
Mammals
Multidisciplinary
Stem Cells
Eukaryota
MicroRNA
Cell Differentiation
purl.org/becyt/ford/3.1 [https]
Cell biology
Nucleic acids
Medicina Básica
Connective Tissue
KLF4
Vertebrates
Medicine
purl.org/becyt/ford/3 [https]
Cellular Types
Anatomy
Stem cell
Reprogramming
Research Article
Pluripotency
Homeobox protein NANOG
CIENCIAS MÉDICAS Y DE LA SALUD
Science
Cell Potency
Rex1
Neurociencias
Induced Pluripotent Stem Cells
Equines
Biology
Kruppel-Like Factor 4
03 medical and health sciences
stem cells
microRNA
Genetics
Animals
Horses
Non-coding RNA
Natural antisense transcripts
Biology and life sciences
Gene Expression Profiling
Embryos
Organisms
Cell Biology
Fibroblasts
Gene regulation
MicroRNAs
Biological Tissue
030104 developmental biology
Amniotes
RNA
Gene expression
Developmental Biology
Zdroj: PLoS ONE
PLoS ONE, Vol 13, Iss 12, p e0207074 (2018)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
ISSN: 1932-6203
Popis: Cell reprogramming has been well described in mouse and human cells. The expression of specific microRNAs has demonstrated to be essential for pluripotent maintenance and cell differentiation, but not much information is available in domestic species. We aim to generate horse iPSCs, characterize them and evaluate the expression of different microRNAs (miR-302a,b,c,d, miR-205, miR-145, miR-9, miR-96, miR-125b and miR-296). Two equine iPSC lines (L2 and L3) were characterized after the reprogramming of equine fibroblasts with the four human Yamanaka‘s factors (OCT-4/SOX-2/c-MYC/KLF4). The pluripotency of both lines was assessed by phosphatase alkaline activity, expression of OCT-4, NANOG and REX1 by RT-PCR, and by immunofluorescence of OCT-4, SOX-2 and c-MYC. In vitro differentiation to embryo bodies (EBs) showed the capacity of the iPSCs to differentiate into ectodermal, endodermal and mesodermal phenotypes. MicroRNA analyses resulted in higher expression of the miR-302 family, miR-9 and miR-96 in L2 and L3 vs. fibroblasts (p
Databáze: OpenAIRE