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Related Concept Videos

Introduction to Fibroblasts01:09

Introduction to Fibroblasts

Rudolph Virchow discovered spindle-shaped cells called fibroblasts in 1858. Inactive fibroblasts, called fibrocytes, become activated by various stimuli, such as growth factors and inflammatory cytokines. Activated fibroblasts play a crucial role in wound healing, inflammation, formation of new blood vessels, and cancer progression. Uncontrolled activation of fibroblasts results in fibrosis, the excess deposition of fibrous tissue, which can lead to scarring and affect normal organs. This...
EPS and iPS Cells in Disease Research01:21

EPS and iPS Cells in Disease Research

Embryonic and induced pluripotent stem cells are excellent models for disease research because of their ability to self-renew and differentiate into most cell types. Somatic cells from a patient are isolated and reprogrammed into induced pluripotent stem cells or iPSCs. These iPSCs are later differentiated into the desired cell type, which mirrors the diseased cell of the patient. In this way, disease models have been created for investigating diseases such as Down syndrome, type I diabetes,...
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...
iPS Cell Differentiation01:22

iPS Cell Differentiation

The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.

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Related Experiment Video

Updated: Jun 11, 2026

RNA-based Reprogramming of Human Primary Fibroblasts into Induced Pluripotent Stem Cells
11:38

RNA-based Reprogramming of Human Primary Fibroblasts into Induced Pluripotent Stem Cells

Published on: November 26, 2018

When fibroblasts MET iPSCs.

Jose M Polo1, Konrad Hochedlinger

  • 1Howard Hughes Medical Institute at Massachusetts General Hospital, Cancer Center, 185 Cambridge Street, Boston, MA 02114, USA.

Cell Stem Cell
|July 13, 2010
PubMed
Summary
This summary is machine-generated.

Induced pluripotent stem cells (iPSCs) arise from a mesenchymal-to-epithelial transition, a process crucial for reprogramming. This finding reveals striking parallels between cellular reprogramming, development, and cancer progression.

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CRISPR/Cas9 Technology in Restoring Dystrophin Expression in iPSC-Derived Muscle Progenitors
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Last Updated: Jun 11, 2026

RNA-based Reprogramming of Human Primary Fibroblasts into Induced Pluripotent Stem Cells
11:38

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Published on: November 26, 2018

Isolation of Adult Human Dermal Fibroblasts from Abdominal Skin and Generation of Induced Pluripotent Stem Cells Using a Non-Integrating Method
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Isolation of Adult Human Dermal Fibroblasts from Abdominal Skin and Generation of Induced Pluripotent Stem Cells Using a Non-Integrating Method

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Area of Science:

  • Stem cell biology
  • Cellular reprogramming
  • Developmental biology
  • Cancer biology

Background:

  • Induced pluripotent stem cells (iPSCs) offer a powerful tool for regenerative medicine and disease modeling.
  • Understanding the initial events in iPSC derivation is key to improving reprogramming efficiency.

Discussion:

  • Two independent studies highlight the mesenchymal-to-epithelial transition (MET) as a critical early step in iPSC generation from fibroblasts.
  • This MET process mirrors events observed during embryonic development and cancer progression.

Key Insights:

  • The MET is a conserved and fundamental cellular process across different biological contexts.
  • Fibroblast reprogramming into iPSCs involves a developmental-like transition.

Outlook:

  • Further research into MET could optimize iPSC generation protocols.
  • Exploring MET similarities may provide new insights into developmental disorders and cancer therapies.