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Mechanisms and models of somatic cell reprogramming

TLDR
Whitehead Institute for Biomedical Research (Jerome and Florence Brill Graduate Student Fellowship) as discussed by the authors ) was the first recipient of the WBIR grant. But this work was performed in a supervised setting.
Abstract
Whitehead Institute for Biomedical Research (Jerome and Florence Brill Graduate Student Fellowship)

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Direct Induction of the Three Pre-implantation Blastocyst Cell Types from Fibroblasts.

TL;DR: Mechanistically, it is shown that the interplay between Esrrb and Eomes during the reprogramming process determines cell fate, where high levels of EsRRb induce a XEN-like state that drives pluripotency and high Levels of Eomes drive trophectodermal fate.
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Cell engineering: Biophysical regulation of the nucleus.

TL;DR: This review will highlight the recent progress in nuclear biomechanics and mechanobiology in the context of cell engineering, tissue remodeling and disease development.
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Defining Reprogramming Checkpoints from Single-Cell Analyses of Induced Pluripotency.

TL;DR: A critical role for signaling inhibition by 2i in repressing somatic expression is identified and synergy between the epigenomic modifiers ascorbic acid and a Dot1L inhibitor for pluripotency gene activation is identified.
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Transcription factor-mediated reprogramming toward hematopoietic stem cells

TL;DR: This review will integrate the recently reported strategies to directly convert a variety of starting cell types toward HSCs in the context of hematopoietic transcriptional regulation and discuss how these findings could be further developed toward the ultimate generation of therapeutic human H SCs.
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Methylated cis-regulatory elements mediate KLF4-dependent gene transactivation and cell migration.

TL;DR: The biological function of mCpG-dependent gene regulation by KLF4 in glioblastoma cells is reported, demonstrating a new paradigm of DNA methylation-mediated gene activation and chromatin remodeling, and providing a general framework to dissect the biological functions ofDNA methylation readers and effectors.
References
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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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Model-based Analysis of ChIP-Seq (MACS)

TL;DR: This work presents Model-based Analysis of ChIP-Seq data, MACS, which analyzes data generated by short read sequencers such as Solexa's Genome Analyzer, and uses a dynamic Poisson distribution to effectively capture local biases in the genome, allowing for more robust predictions.
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Core transcriptional regulatory circuitry in human embryonic stem cells.

TL;DR: Insight is provided into the transcriptional regulation of stem cells and how OCT4, SOX2, and NANOG contribute to pluripotency and self-renewal and how they collaborate to form regulatory circuitry consisting of autoregulatory and feedforward loops.
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Generation of induced pluripotent stem cells without Myc from mouse and human fibroblasts

TL;DR: A modified protocol for the generation of iPS cells that does not require the Myc retrovirus is described and, with this protocol, significantly fewer non-iPS background cells are obtained, and theiPS cells generated were consistently of high quality.