Human Ips Cells

Human induced pluripotent stem (iPS) cells are mature human cells reprogrammed to an embryonic-like, pluripotent state, enabling them to generate many specialized cell types for research and disease modeling. Reprogramming typically introduces defined transcription factors that reset the cell’s gene-expression and epigenetic programs, after which directed culture conditions guide differentiation into neural progenitors, neurons, or glial cells. In neuroscience, human iPS cells support studies of brain development, neurodegenerative and neuropsychiatric disorders, and patient-specific cellular phenotypes. They also provide platforms for testing therapies and investigating disease mechanisms in human-derived neural cells, complementing animal models and primary tissue studies.

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Research

JoVE EoE - Genome Editing Techniques

PiggyBac Transposon-Mediated Gene Editing in Human iPSCs: A Procedure to Integrate Gene of Interest in Human iPSCs Using PiggyBac Transposon System

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2025

This video demonstrates the procedure to generate motor neurons by transfection of human iPSCs with PiggyBac transposon system by the ectopic expression of lineage-specific transcription factors.

Small-scale Propagation of Human iPSCs in Serum-free Conditions for Routine Immunocytochemical Characterization

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2017

Regular characterization of induced pluripotent stem cells (iPSCs), to ascertain maintenance of their pluripotent state, is an important step before these cells are used for other applications. Here we describe a method for the small-scale propagation of human iPSCs specifically designed to enable their easy and routine characterization via immunocytochemistry.

Efficient Generation and Editing of Feeder-free IPSCs from Human Pancreatic Cells Using the CRISPR-Cas9 System

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Cited by 4 •

2017

This protocol describes in detail the generation of footprint-free induced pluripotent stem cells (iPSCs) from human pancreatic cells in feeder-free conditions, followed by editing using CRISPR/Cas9 ribonucleoproteins and characterization of the modified single-cell clones.

Generation of iPSC-derived Human Brain Organoids to Model Early Neurodevelopmental Disorders

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Cited by 46 •

2017

Modeling human brain development has been hindered due to the unprecedented complexity of neural epithelial tissue. Here, a method for the robust generation of brain organoids to delineate early events of human brain development and to model microcephaly in vitro is described.

Developing Human iPSC-Derived Motor Nerve Organoids Using a Microfluidic Chip

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2025

This video demonstrates the method of creating motor nerve organoids by first culturing human induced pluripotent stem cells in a special medium to form spheroids, then differentiating them into motor neurons using specific inhibitors, and finally cultivating them in a microfluidic chip to extend axons and form motor nerve organoids.

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