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Neurosphere Based Differentiation of Human iPSC Improves Astrocyte Differentiation

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TLDR
It is determined that culturing iPSC-derived NPCs as three-dimensional (3D) floating neurospheres resulted in increased expression of the neural progenitor cell (NPC) markers, PAX6 and NESTIN, and the 3D propagation method could constitute a useful tool to promote NPC homogeneity and also to increase the differentiation potential of iPSCs towards astrocytes.
Abstract
Neural progenitor cells (NPCs) derived from human induced pluripotent stem cells (iPSCs) are traditionally maintained and proliferated utilizing two-dimensional (2D) adherent monolayer culture systems. However, NPCs cultured using this system hardly reflect the intrinsic spatial development of brain tissue. In this study, we determined that culturing iPSC-derived NPCs as three-dimensional (3D) floating neurospheres resulted in increased expression of the neural progenitor cell (NPC) markers, PAX6 and NESTIN. Expansion of NPCs in 3D culture methods also resulted in a more homogenous PAX6 expression when compared to 2D culture methods. Furthermore, the 3D propagation method for NPCs resulted in a significant higher expression of the astrocyte markers  GFAP and aquaporin 4 (AQP4) in the differentiated cells. Thus, our 3D propagation method could constitute a useful tool to promote NPC homogeneity and also to increase the differentiation potential of iPSC towards astrocytes.

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Astrocyte Differentiation of Human Pluripotent Stem Cells: New Tools for Neurological Disorder Research

TL;DR: The aim of this review article is to compare and summarize the currently available protocols and their strategies to generate human astrocytes from pluripotent stem cells (PSCs), and to discuss the potential role of human-induced PSCs derived astroCytes in disease modeling.
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Neural Crest Cell Implantation Restores Enteric Nervous System Function and Alters the Gastrointestinal Transcriptome in Human Tissue-Engineered Small Intestine

TL;DR: RNA sequencing identified differentially expressed genes involved in neurogenesis, gliogenesis, gastrointestinal tract development, and differentiated epithelial cell types when ENS elements are restored during in vivo development of HIO-TESI.
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Genetic predispositions of Parkinson's disease revealed in patient-derived brain cells.

TL;DR: The interplay between genetic predispositions and midbrain neuronal impairments in people living with PD is discussed and the understanding of robust cellular phenotypes across genetic cohorts of Parkinson’s patients may guide future personalized drug screens in preclinical research.
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Fast Generation of Functional Subtype Astrocytes from Human Pluripotent Stem Cells.

TL;DR: A simple and efficient method to efficiently generate astrocytes in 4–7 weeks by using CRISPR/Cas9-mediated inducible expression of NFIA or NFIA plus SOX9 in hPSCs and a strategy to generate region-specificAstrocyte subtypes by combining differentiation of regional progenitors and transgenic induction of astroCytes.
References
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Analysis of relative gene expression data using real-time quantitative pcr and the 2(-delta delta c(t)) method

TL;DR: The 2-Delta Delta C(T) method as mentioned in this paper was proposed to analyze the relative changes in gene expression from real-time quantitative PCR experiments, and it has been shown to be useful in the analysis of realtime, quantitative PCR data.
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TL;DR: It is demonstrated that iPS cells can be generated from adult human fibroblasts with the same four factors: Oct3/4, Sox2, Klf4, and c-Myc.
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Embryonic Stem Cell Lines Derived from Human Blastocysts

TL;DR: Human blastocyst-derived, pluripotent cell lines are described that have normal karyotypes, express high levels of telomerase activity, and express cell surface markers that characterize primate embryonic stem cells but do not characterize other early lineages.
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TL;DR: Before the full potential of neural stem cells can be realized, the authors need to learn what controls their proliferation, as well as the various pathways of differentiation available to their daughter cells.
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