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Related Concept Videos

Replicative Cell Senescence02:15

Replicative Cell Senescence

Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
Replicative Cell Senescence02:15

Replicative Cell Senescence

Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds the telomeric...
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...
Molecular Factors Affecting Cell Division01:27

Molecular Factors Affecting Cell Division

Several external and internal factors influence the initiation and inhibition of cell division. For instance, the death of nearby cells or the release of human growth hormone (hGH) promotes cell division. In contrast, lack of hGH or crowding of cells can inhibit cell division.
Several proteins function as internal regulators to ensure each cell cycle stage is completed faithfully before proceeding to the next. Regulator molecules may act directly or influence the activity or production of other...
Regulation of Hematopoietic Stem Cells01:01

Regulation of Hematopoietic Stem Cells

All blood and immune cells are produced from the multipotent hematopoietic stem cells (HSCs) by the process of hematopoiesis. However, they all have a limited life span. In addition, many are depleted in immune surveillance or combatting an injury or infection. This makes blood one of the most regenerative tissues. Hematopoiesis helps replenish these blood and immune cells, restoring the body's normal functioning. However, overproduction of blood and immune cells can make them cancerous or...
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...

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A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae
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Published on: September 17, 2020

Mechanisms that regulate stem cell aging and life span.

Robert A J Signer1, Sean J Morrison

  • 1Children's Research Institute, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.

Cell Stem Cell
|February 12, 2013
PubMed
Summary
This summary is machine-generated.

Stem cell function declines with age due to various cellular and environmental factors, impacting tissue regeneration and disease. Understanding these changes is crucial for addressing age-related health issues.

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Last Updated: May 14, 2026

A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae
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A Suppressor Screen for the Characterization of Genetic Links Regulating Chronological Lifespan in Saccharomyces cerevisiae

Published on: September 17, 2020

Collection of Serum- and Feeder-free Mouse Embryonic Stem Cell-conditioned Medium for a Cell-free Approach
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Techniques to Induce and Quantify Cellular Senescence
06:51

Techniques to Induce and Quantify Cellular Senescence

Published on: May 1, 2017

Area of Science:

  • Gerontology
  • Stem Cell Biology
  • Molecular Biology

Background:

  • Mammalian aging is characterized by impaired tissue regeneration, increased degenerative diseases, and higher cancer incidence.
  • Stem cells are vital for tissue repair but can accumulate mutations, contributing to cancer development.
  • Age-related declines in stem cell function are observed across multiple tissues.

Purpose of the Study:

  • To investigate the impact of age-related stem cell dysfunction on organismal longevity.
  • To explore the mechanisms underlying stem cell aging, including tumor suppressor expression, DNA damage, and altered cellular physiology.
  • To understand the interplay between longevity mechanisms and age-related morbidity via stem cell modulation.

Main Methods:

  • Review of existing literature on stem cell aging and longevity.
  • Analysis of molecular and cellular changes in aged stem cells.
  • Examination of the relationship between stem cell function and age-related diseases.

Main Results:

  • Stem cell function declines with age due to factors like increased tumor suppressor expression and DNA damage.
  • Altered cellular physiology and tissue microenvironments also contribute to stem cell aging.
  • The precise influence of stem cell decline on organismal longevity remains an open question.

Conclusions:

  • Age-related stem cell dysfunction is a significant factor in reduced tissue regeneration and increased disease susceptibility.
  • Mechanisms governing longevity likely influence age-related morbidity through their effects on stem cells.
  • Further research is needed to elucidate the direct link between stem cell aging and lifespan.