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Somatic to iPS Cell Reprogramming01:29

Somatic to iPS Cell Reprogramming

Reprogramming alters the gene expression in somatic cells, transforming them into induced pluripotent stem (iPS) cells over several generations. Scientists can reprogram cells by introducing genes for four transcription factors—Oct4, Sox2, Klf4, and c-Myc (OSKM) by viral or non-viral methods. These factors are also known as Yamanaka factors after Shinya Yamanaka, who first generated iPS cells using mouse skin cells. Yamanaka was awarded the Nobel Prize in Physiology or Medicine in 2012 for this...
Lineage Commitment01:21

Lineage Commitment

Commitment is the  process whereby stem cells:
Methods of Nuclear Reprogramming01:24

Methods of Nuclear Reprogramming

Nuclear reprogramming is a process of transforming one cell type into an unrelated cell type by epigenetic changes that alter the cell’s original gene expression pattern. Such epigenetic changes force cells to express a different set of genes, which play a significant role in inducing transformation into other cell types. Nuclear reprogramming offers applications in reproductive cloning for livestock propagation and regenerative medicine — developing patient-specific cells for injury repair.
Chromatin Modification in iPS Cells01:32

Chromatin Modification in iPS Cells

Chromatin modification alters gene expression; therefore, scientists can add histone-modifying enzymes, histone variants, and chromatin remodeling complexes to somatic cells to aid reprogramming into pluripotent stem (iPS) cells.
Compact chromatin makes reprogramming difficult. Enzymes, such as histone demethylases and acetyltransferases, are often added during reprogramming to loosen the chromatin, making the DNA more accessible to transcription factors. Molecules that inhibit histone...
Maintenance of the ES Cell State01:14

Maintenance of the ES Cell State

The cells of the blastocyst inner cell mass only remain pluripotent for a short time. This state of pluripotency and self-renewal can be maintained in embryonic stem (ES) cell culture by adding specific chemicals or growth factors to ensure the cells can continue dividing and later differentiate into different cell types. In some cases, the cells are grown on a feeder layer of differentiated cells, which provides the growth factors and extracellular matrix components necessary for stem cell...
Induced Pluripotent Stem Cells01:13

Induced Pluripotent Stem Cells

Stem cells are undifferentiated cells that divide and produce different types of cells. Ordinarily, cells that have differentiated into a specific cell type are post-mitotic—that is, they no longer divide. However, scientists have found a way to reprogram these mature cells so that they “de-differentiate” and return to an unspecialized, proliferative state. These cells are also pluripotent like embryonic stem cells—able to produce all cell types—and are therefore called induced pluripotent stem...

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Endogenous Mobilization of Bone-Marrow Cells Into the Murine Retina Induces Fusion-Mediated Reprogramming of Müller Glia Cells.

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Related Experiment Video

Updated: Jun 4, 2026

Reprogramming Pancreatic Ductal Adenocarcinoma to Pluripotency
07:08

Reprogramming Pancreatic Ductal Adenocarcinoma to Pluripotency

Published on: February 2, 2024

Reprogramming cell fate to pluripotency: the decision-making signalling pathways.

Daniela Sanges1, Maria-Pia Cosma

  • 1Center for Genomic Regulation (CRG), Barcelona, Spain.

The International Journal of Developmental Biology
|February 10, 2011
PubMed
Summary

Cell differentiation may be reversible. Recent studies show somatic cells can regain pluripotency, challenging previous assumptions about developmental biology and offering new insights into reprogramming mechanisms.

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A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening
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A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening

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Cell Surface Marker Mediated Purification of iPS Cell Intermediates from a Reprogrammable Mouse Model
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Cell Surface Marker Mediated Purification of iPS Cell Intermediates from a Reprogrammable Mouse Model

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Last Updated: Jun 4, 2026

Reprogramming Pancreatic Ductal Adenocarcinoma to Pluripotency
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A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening
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Cell Surface Marker Mediated Purification of iPS Cell Intermediates from a Reprogrammable Mouse Model
10:32

Cell Surface Marker Mediated Purification of iPS Cell Intermediates from a Reprogrammable Mouse Model

Published on: September 6, 2014

Area of Science:

  • Developmental Biology
  • Stem Cell Biology
  • Cellular Reprogramming

Background:

  • Pluripotency, the ability of a cell to differentiate into all lineages of the mature organism, was traditionally considered irreversibly lost during development.
  • This progressive loss was thought to involve strict coordination of signaling pathways regulating cell proliferation, differentiation, and migration.

Purpose of the Study:

  • To re-evaluate the reversibility of cell differentiation in light of new evidence.
  • To review signaling pathways that promote the acquisition and maintenance of pluripotency.
  • To discuss the mechanisms underlying nuclear reprogramming of somatic cells.

Main Methods:

  • Review of recent scientific literature and breakthroughs in cellular reprogramming.
  • Analysis of evidence regarding the reprogramming of terminally differentiated cells into pluripotent stem cells.
  • Examination of the role of specific transcription factors and signaling pathways in somatic cell reprogramming.

Main Results:

  • Terminally differentiated cells can be reprogrammed into pluripotent stem cells, challenging the notion of irreversible differentiation.
  • Ectopic expression of specific transcription factors can induce pluripotency in somatic cells.
  • Modulation of key signaling pathways, including Wnt/beta-catenin, MAPK/ERK, TGF-beta, and PI3K/Akt, significantly enhances somatic cell reprogramming.

Conclusions:

  • Cell differentiation is not necessarily irreversible, and pluripotency can be re-acquired.
  • Signaling pathways play a crucial role in promoting and maintaining pluripotency during reprogramming.
  • Further research is needed to fully elucidate the mechanisms of nuclear reprogramming.