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Journal ArticleDOI

Biophysical regulation of epigenetic state and cell reprogramming

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TLDR
It is shown that biophysical cues, in the form of parallel microgrooves on the surface of cell-adhesive substrates, can replace the effects of small-molecule epigenetic modifiers and significantly improve reprogramming efficiency and promote a mesenchymal-to-epithelial transition in adult fibroblasts.
Abstract
Somatic cells can be reprogrammed into induced pluripotent stem cells biochemically through the expression of a few transcription factors. It is now shown that aligned microgrooves or nanofibres on cell-adhesive substrates can promote the reprogramming of somatic cells more efficiently through epigenetic regulation of genes related to pluripotency and the mesenchymal-to-epithelial transition. The findings suggest that the epigenetic state can be regulated by variations in cell morphology.

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Dissertation

Molecular Mechanisms Regulating Somatic Reprogramming

TL;DR: This thesis shows that distinct molecular networks control the acquisition and subsequent maintenance of pluripotency, and reveals the functional role of a new class of RNAs, called long intergenic noncoding RNAs (lincRNAs), in the mesenchymal-to-epithelial transition during the initiation phase.

Mechanochemical control of stem cell biology in development and disease: Experimental and theoretical models

TL;DR: A minimal `scar in a dish' model is developed to clarify the kinetics of tension-sensitive proteins in mesenchymal stem cells (MSCs), which possess plasticity to mechanochemical changes of the microenvironment that are typical of scars.
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.
Journal ArticleDOI

Matrix elasticity directs stem cell lineage specification.

TL;DR: Naive mesenchymal stem cells are shown here to specify lineage and commit to phenotypes with extreme sensitivity to tissue-level elasticity, consistent with the elasticity-insensitive commitment of differentiated cell types.
Journal ArticleDOI

Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells

TL;DR: This article showed that OCT4, SOX2, NANOG, and LIN28 factors are sufficient to reprogram human somatic cells to pluripotent stem cells that exhibit the essential characteristics of embryonic stem (ES) cells.
Journal ArticleDOI

Cell shape, cytoskeletal tension, and rhoa regulate stem cell lineage commitment

TL;DR: It is demonstrated that cell shape regulates commitment of human mesenchymal stem cells to adipocyte or osteoblast fate and mechanical cues experienced in developmental and adult contexts, embodied by cell shape, cytoskeletal tension, and RhoA signaling, are integral to the commitment of stem cell fate.

Supporting Online Material for Induced Pluripotent Stem Cell Lines Derived from Human Somatic Cells

TL;DR: Yu et al. as discussed by the authors proposed online material for induced pluripotent stem cell lines derived from human Somatic Cells, which can be used for transplanting human stem cells to humans.
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