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Related Concept Videos

Cellular Differentiation00:57

Cellular Differentiation

How does a complex organism such as a human develop from a single cell? It all starts from a single fertilized egg which gives rise to a vast array of cell types, such as nerve cells, muscle cells, and epithelial cells that characterize the adult? Throughout development and adulthood, cellular differentiation leads cells to assume their final morphology and physiology. Differentiation is the process by which unspecialized cells become specialized to carry out distinct functions.
A zygote is a...
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...
Stem Cell Niche01:26

Stem Cell Niche

The stem cell niche is the dynamic microenvironment where stem cells reside. Inside these niches, the cells may remain undifferentiated, undergo high self-renewal, or become lineage-specific progenitors. Stem cells coexist with other niche cells, such as stromal cells. They also interact closely with the ECM. Cell-cell and cell-matrix communication occur via adhesion molecules or soluble factors that signal the stem cells and determine their fate. Stromal cells also provide survival signals to...
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.
Tissue Renewal without Stem Cells01:23

Tissue Renewal without Stem Cells

After cellular or tissue damage, the resident stem cells present in the human body can locally repair and regenerate the damaged tissue or organ. However, even though some tissues do not have stem cells, they can repair and regenerate with the help of pre-existing cells. For example, beta cells of the pancreas and hepatocytes of the liver can divide to renew and regenerate the tissue. Here, both cell division and cell death are well regulated by homeostasis.
However, failure of such a system...
Role Of Notch Signalling In Intestinal Stem Cell Renewal01:12

Role Of Notch Signalling In Intestinal Stem Cell Renewal

Notch signaling was first discovered in Drosophila melanogaster, where it is involved in cell lineage differentiation. Notch signaling regulates the maintenance and differentiation of intestinal stem cells or ISCs by controlling the expression of atonal homolog 1 or Atoh1. Atoh1 directs cells to differentiate into secretory cells.
Direct cell-to-cell contact is needed for the activation of Notch signaling. The signal is initiated when a notch ligand binds to a receptor on an adjacent cell, also...

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Related Experiment Video

Updated: May 22, 2026

Initiating Differentiation in Immortalized Multipotent Otic Progenitor Cells
12:17

Initiating Differentiation in Immortalized Multipotent Otic Progenitor Cells

Published on: January 2, 2016

Maintaining differentiated cellular identity.

Johan Holmberg1, Thomas Perlmann

  • 1Ludwig Institute for Cancer Research Ltd, BOX 240, Karolinska Institutet, S-171 77 Stockholm, Sweden. johan.holmberg@licr.ki.se

Nature Reviews. Genetics
|May 19, 2012
PubMed
Summary

Cellular identity is not fixed; differentiated cells can be reprogrammed. This review explores transcriptional mechanisms maintaining stable mature cell identities, crucial for understanding cell fate.

Area of Science:

  • * Cellular reprogramming and developmental biology.
  • * Molecular mechanisms of cell identity maintenance.

Background:

  • * Somatic differentiated cells can be reprogrammed to pluripotency or alternative lineages.
  • * This plasticity highlights the need to understand how cell identity is normally maintained.
  • * Existing research focuses on reprogramming and pluripotency mechanisms.

Purpose of the Study:

  • * To review recent studies on transcriptional control of differentiated states.
  • * To discuss emerging insights into mechanisms of mature cell identity maintenance.

Main Methods:

  • * Literature review of recent studies on transcriptional regulation.
  • * Analysis of findings related to cell identity stability.

Main Results:

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Culture and Maintenance of Human Embryonic Stem Cells
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Culture and Maintenance of Human Embryonic Stem Cells

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Differentiation, Maintenance, and Analysis of Human Retinal Pigment Epithelium Cells: A Disease-in-a-dish Model for BEST1 Mutations
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Differentiation, Maintenance, and Analysis of Human Retinal Pigment Epithelium Cells: A Disease-in-a-dish Model for BEST1 Mutations

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Last Updated: May 22, 2026

Initiating Differentiation in Immortalized Multipotent Otic Progenitor Cells
12:17

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Published on: January 2, 2016

Culture and Maintenance of Human Embryonic Stem Cells
09:36

Culture and Maintenance of Human Embryonic Stem Cells

Published on: December 22, 2009

Differentiation, Maintenance, and Analysis of Human Retinal Pigment Epithelium Cells: A Disease-in-a-dish Model for BEST1 Mutations
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Differentiation, Maintenance, and Analysis of Human Retinal Pigment Epithelium Cells: A Disease-in-a-dish Model for BEST1 Mutations

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  • * Differentiated cell states are not irreversible.
  • * Transcriptional mechanisms play a key role in maintaining cell identity.
  • * New insights are emerging on stable cell fate determination.

Conclusions:

  • * Understanding cell identity maintenance is critical, given the plasticity of differentiated cells.
  • * Transcriptional control is central to preserving mature cell identities.
  • * Further research is needed to fully elucidate these mechanisms.