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1.
Sci Rep ; 8(1): 2942, 2018 02 13.
Article in English | MEDLINE | ID: mdl-29440666

ABSTRACT

Neural tube defects (NTDs) are severe congenital abnormalities, caused by failed closure of neural tube during early embryonic development. Periconceptional folic acid (FA) supplementation greatly reduces the risk of NTDs. However, the molecular mechanisms behind NTDs and the preventive role of FA remain unclear. Here, we use human induced pluripotent stem cells (iPSCs) derived from fetuses with spina bifida aperta (SBA) to study the pathophysiology of NTDs and explore the effects of FA exposure. We report that FA exposure in SBA model is necessary for the proper formation and maturation of neural tube structures and robust differentiation of mesodermal derivatives. Additionally, we show that the folate antagonist methotrexate dramatically affects the formation of neural tube structures and FA partially reverts this aberrant phenotype. In conclusion, we present a novel model for human NTDs and provide evidence that it is a powerful tool to investigate the molecular mechanisms underlying NTDs, test drugs for therapeutic approaches.


Subject(s)
Folic Acid/pharmacology , Induced Pluripotent Stem Cells/drug effects , Phenotype , Spina Bifida Cystica/pathology , Cell Differentiation/drug effects , Down-Regulation/drug effects , Humans , Induced Pluripotent Stem Cells/cytology , Induced Pluripotent Stem Cells/metabolism , Muscle Development/drug effects , Neurons/cytology , Neurons/drug effects , PAX3 Transcription Factor/genetics , PAX7 Transcription Factor/genetics , Spheroids, Cellular/cytology , Spheroids, Cellular/drug effects , Up-Regulation/drug effects
2.
Stem Cell Reports ; 10(2): 655-672, 2018 02 13.
Article in English | MEDLINE | ID: mdl-29337119

ABSTRACT

Scarce access to primary samples and lack of efficient protocols to generate oligodendrocytes (OLs) from human pluripotent stem cells (hPSCs) are hampering our understanding of OL biology and the development of novel therapies. Here, we demonstrate that overexpression of the transcription factor SOX10 is sufficient to generate surface antigen O4-positive (O4+) and myelin basic protein-positive OLs from hPSCs in only 22 days, including from patients with multiple sclerosis or amyotrophic lateral sclerosis. The SOX10-induced O4+ population resembles primary human OLs at the transcriptome level and can myelinate neurons in vivo. Using in vitro OL-neuron co-cultures, myelination of neurons by OLs can also be demonstrated, which can be adapted to a high-throughput screening format to test the response of pro-myelinating drugs. In conclusion, we provide an approach to generate OLs in a very rapid and efficient manner, which can be used for disease modeling, drug discovery efforts, and potentially for therapeutic OL transplantation.


Subject(s)
Cell Differentiation/genetics , Oligodendroglia/metabolism , Pluripotent Stem Cells/metabolism , SOXE Transcription Factors/genetics , Amyotrophic Lateral Sclerosis/genetics , Amyotrophic Lateral Sclerosis/therapy , Antigens, Surface/genetics , Gene Expression Regulation, Developmental , Humans , Multiple Sclerosis/genetics , Multiple Sclerosis/pathology , Multiple Sclerosis/therapy , Myelin Basic Protein/genetics , Neurons/pathology , Neurons/transplantation , Oligodendroglia/cytology , Oligodendroglia/transplantation , Pluripotent Stem Cells/cytology , Pluripotent Stem Cells/transplantation , Transcriptome/genetics
3.
J Vis Exp ; (117)2016 11 20.
Article in English | MEDLINE | ID: mdl-27911376

ABSTRACT

Even with the revolution of gene-targeting technologies led by CRISPR-Cas9, genetic modification of human pluripotent stem cells (hPSCs) is still time consuming. Comparative studies that use recombinant lines with transgenes integrated into safe harbor loci could benefit from approaches that use site-specific targeted recombinases, like Cre or FLPe, which are more rapid and less prone to off-target effects. Such methods have been described, although they do not significantly outperform gene targeting in most aspects. Using Zinc-finger nucleases, we previously created a master cell line in the AAVS1 locus of hPSCs that contains a GFP-Hygromycin-tk expressing cassette, flanked by heterotypic FRT sequences. Here, we describe the procedures to perform FLPe recombinase-mediated cassette exchange (RMCE) using this line. The master cell line is transfected with a RMCE donor vector, which contains a promoterless Puromycin resistance, and with FLPe recombinase. Application of both a positive (Puromycin) and negative (FIAU) selection program leads to the selection of RMCE without random integrations. RMCE generates fully characterized pluripotent polyclonal transgenic lines in 15 d with 100% efficiency. Despite the recently described limitations of the AAVS1 locus, the ease of the system paves the way for hPSC transgenesis in isogenic settings, is necessary for comparative studies, and enables semi-high-throughput genetic screens for gain/loss of function analysis that would otherwise be highly time consuming.


Subject(s)
Pluripotent Stem Cells , Recombination, Genetic , Cell Line , Gene Targeting , Humans , Recombinases , Transgenes
4.
Stem Cell Reports ; 5(5): 918-931, 2015 Nov 10.
Article in English | MEDLINE | ID: mdl-26455413

ABSTRACT

Tools for rapid and efficient transgenesis in "safe harbor" loci in an isogenic context remain important to exploit the possibilities of human pluripotent stem cells (hPSCs). We created hPSC master cell lines suitable for FLPe recombinase-mediated cassette exchange (RMCE) in the AAVS1 locus that allow generation of transgenic lines within 15 days with 100% efficiency and without random integrations. Using RMCE, we successfully incorporated several transgenes useful for lineage identification, cell toxicity studies, and gene overexpression to study the hepatocyte lineage. However, we observed unexpected and variable transgene expression inhibition in vitro, due to DNA methylation and other unknown mechanisms, both in undifferentiated hESC and differentiating hepatocytes. Therefore, the AAVS1 locus cannot be considered a universally safe harbor locus for reliable transgene expression in vitro, and using it for transgenesis in hPSC will require careful assessment of the function of individual transgenes.


Subject(s)
Embryonic Stem Cells/metabolism , Gene Targeting/methods , Hepatocytes/cytology , Induced Pluripotent Stem Cells/metabolism , Recombinases/metabolism , Transgenes , Cells, Cultured , DNA Methylation , Dependovirus/genetics , Embryonic Stem Cells/cytology , Gene Silencing , Genetic Loci , Hepatocytes/metabolism , Humans , Induced Pluripotent Stem Cells/cytology , Recombinases/genetics
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