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Cerebral organoids model human brain development and microcephaly

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TLDR
A human pluripotent stem cell-derived three-dimensional organoid culture system that develops various discrete, although interdependent, brain regions that include a cerebral cortex containing progenitor populations that organize and produce mature cortical neuron subtypes is developed.
Abstract
The complexity of the human brain has made it difficult to study many brain disorders in model organisms, highlighting the need for an in vitro model of human brain development Here we have developed a human pluripotent stem cell-derived three-dimensional organoid culture system, termed cerebral organoids, that develop various discrete, although interdependent, brain regions These include a cerebral cortex containing progenitor populations that organize and produce mature cortical neuron subtypes Furthermore, cerebral organoids are shown to recapitulate features of human cortical development, namely characteristic progenitor zone organization with abundant outer radial glial stem cells Finally, we use RNA interference and patient-specific induced pluripotent stem cells to model microcephaly, a disorder that has been difficult to recapitulate in mice We demonstrate premature neuronal differentiation in patient organoids, a defect that could help to explain the disease phenotype Together, these data show that three-dimensional organoids can recapitulate development and disease even in this most complex human tissue

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Tumor organoids: synergistic applications, current challenges, and future prospects in cancer therapy

TL;DR: In this paper, the authors discuss various methods for the creation of cancer organoids and summarize organ-specific advances and applications, synergistic technologies, and treatments as well as current limitations and future prospects for cancer organoid.
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Harnessing the Potential of Human Pluripotent Stem Cells and Gene Editing for the Treatment of Retinal Degeneration

TL;DR: This brief review will discuss some of the issues that should be taken into account when carrying out disease modelling and gene editing of retinal cells and the use of human induced pluripotent stem cells (iPSCs), and the importance of using isogenic iPSC lines as controls.
Journal ArticleDOI

Directed midbrain and spinal cord neurogenesis from pluripotent stem cells to model development and disease in a dish

TL;DR: Recent advances in neuronal fate induction in vitro are reviewed, with a focus on the interplay between cell intrinsic and extrinsic factors, and the implications for studying development and disease in a dish are discussed.
Journal ArticleDOI

Electrophysiological Analysis of Brain Organoids: Current Approaches and Advancements

TL;DR: A review of electrophysiological technologies and analytical methods for brain organoid analysis is presented in this paper, with a focus on advances with applicability to brain organoids analysis.
References
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Journal ArticleDOI

Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors.

TL;DR: Induction of pluripotent stem cells from mouse embryonic or adult fibroblasts by introducing four factors, Oct3/4, Sox2, c-Myc, and Klf4, under ES cell culture conditions is demonstrated and iPS cells, designated iPS, exhibit the morphology and growth properties of ES cells and express ES cell marker genes.
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Single Lgr5 stem cells build crypt-villus structures in vitro without a mesenchymal niche.

TL;DR: It is concluded that intestinal crypt–villus units are self-organizing structures, which can be built from a single stem cell in the absence of a non-epithelial cellular niche.
Journal ArticleDOI

Generation of germline-competent induced pluripotent stem cells

TL;DR: iPS cells competent for germline chimaeras can be obtained from fibroblasts, but retroviral introduction of c-Myc should be avoided for clinical application.
Journal ArticleDOI

A ROCK inhibitor permits survival of dissociated human embryonic stem cells

TL;DR: Application of a selective Rho-associated kinase (ROCK) inhibitor, Y-27632, to hES cells markedly diminishes dissociation-induced apoptosis, increases cloning efficiency and facilitates subcloning after gene transfer, and enables SFEB-cultured hES Cells to survive and differentiate into Bf1+ cortical and basal telencephalic progenitors.
Journal ArticleDOI

The cell biology of neurogenesis.

TL;DR: In this paper, the authors discuss how these features change during development from neuroepithelial to radial glial cells, and how this transition affects cell fate and neurogenesis.
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