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Related Concept Videos

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...
Lineage Commitment01:21

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Commitment is the  process whereby stem cells:
Embryonic Stem Cells00:57

Embryonic Stem Cells

Embryonic stem (ES) cells were first discovered in mice in 1981 by Martin Evans. In 1998, James Thomson identified a method to isolate embryonic stem cells from humans. Human embryonic stem cells (hESCs) are obtained from 3-5 day old embryos that remain unused after an in vitro fertilization procedure.
ES cells are grown in a culture medium where they can divide indefinitely, creating ES cell lines. Under certain conditions, ES cells can differentiate, either spontaneously into a variety of...
Embryonic Stem Cells00:58

Embryonic Stem Cells

Embryonic stem (ES) cells are undifferentiated pluripotent cells, meaning they can produce any cell type in the body. This gives them tremendous potential in science and medicine since they can generate specific cell types for use in research or to replace body cells lost due to damage or disease.
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...
Source And Potency Of Stem Cells01:27

Source And Potency Of Stem Cells

Stem cells are undifferentiated cells with extensive self-renewal properties that help them maintain their population during the fetal and adult stages of life. They can specialize in all cell types of the human body. However, their differential potential may vary and can be classified into five types. Stem cells can be (1) Totipotent, (2) Pluripotent, (3) Multipotent, (4) Oligopotent, and (5) Unipotent. Each stem cell has a specific origin; the fertilized egg or zygote is a totipotent cell and...

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Epigenetic Regulation of Cardiac Differentiation of Embryonic Stem Cells and Tissues
13:03

Epigenetic Regulation of Cardiac Differentiation of Embryonic Stem Cells and Tissues

Published on: June 3, 2016

Epigenetics, stem cells and epithelial cell fate.

Audrey Vincent1, Isabelle Van Seuningen

  • 1Inserm, U837, Jean-Pierre Aubert Research Center, Team 5 Mucins, epithelial differentiation and carcinogenesis, Place de Verdun, 59045 Lille Cedex, France.

Differentiation; Research in Biological Diversity
|July 28, 2009
PubMed
Summary
This summary is machine-generated.

Epigenetic profiles guide cell differentiation by regulating gene expression. Understanding these mechanisms in intestinal stem cells is key to deciphering developmental and cancerous processes.

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Area of Science:

  • Developmental Biology
  • Epigenetics
  • Cell Biology

Background:

  • Epigenetic profiles are crucial for cell differentiation, enabling stem cells with identical genes to develop distinct cell fates.
  • Chromatin modifier enzymes (e.g., DNA methyltransferases, histone deacetylases) are vital for establishing transcriptional programs during cell differentiation.
  • While studied in various cell types, intestinal stem cell niches offer a unique model for investigating epigenetic programming.

Purpose of the Study:

  • To review the role of epigenetic modifications in cell differentiation, focusing on epithelial cells of the digestive tract.
  • To highlight intestinal stem cell niches as a model system for understanding epigenetic control of nuclear programming.
  • To underscore the importance of decoding epigenetic mechanisms for understanding both normal development and cancer.

Main Methods:

  • Literature review focusing on epigenetic mechanisms in cell differentiation.
  • Analysis of studies involving chromatin modifier enzymes.
  • Examination of research on intestinal stem cell niches and epithelial cell differentiation.

Main Results:

  • Epigenetic programming dictates selective gene expression patterns essential for cell fate determination.
  • Chromatin modifiers play fundamental roles in orchestrating gene expression during cell differentiation.
  • Intestinal stem cells serve as a valuable model for studying how epigenetic changes drive differentiation.

Conclusions:

  • Epigenetic mechanisms are fundamental to cell differentiation and development.
  • Dysregulation of epigenetic programming is implicated in human tumors.
  • Further research into epigenetic programming is essential for understanding development and cancer.