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Related Concept Videos

The Effect of Aging on Tissues01:19

The Effect of Aging on Tissues

Several body functions deteriorate with age. The external signs of aging are easily identifiable. For example, the skin becomes dry, less elastic, and thins out, forming wrinkles. The skin of the face begins to appear looser due to a decrease in the levels of elastic and collagen fibers in the connective tissue. Additionally, melanin production in the hair follicle decreases with age, resulting in gray hair. Moreover, the senses of sight and hearing decline, so glasses and hearing aids may...
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...
Forced Transdifferentiation01:28

Forced Transdifferentiation

Transdifferentiation, also known as lineage reprogramming, was first discovered by Selman and Kafatos in 1974 in silkmoths. They observed that the moths’ cuticle-producing cells transformed into salt-producing cells. Many such cases of natural transdifferentiation occur in organisms. In humans, pancreatic alpha cells can become beta cells. In newts, the loss of the eye’s lens causes the pigmented epithelial cells to transdifferentiate into the lens cells.
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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.
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...
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.
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Related Experiment Video

Updated: May 20, 2026

Peptides from Phage Display Library Modulate Gene Expression in Mesenchymal Cells and Potentiate Osteogenesis in Unicortical Bone Defects
07:53

Peptides from Phage Display Library Modulate Gene Expression in Mesenchymal Cells and Potentiate Osteogenesis in Unicortical Bone Defects

Published on: December 10, 2010

Peptides tissue-specifically stimulate cell differentiation during their aging.

V Kh Khavinson1, N S Linkova, V O Polyakova

  • 1I. P. Pavlov Institute of Physiology, Russian Academy of Sciences, St. Petersburg, Russia.

Bulletin of Experimental Biology and Medicine
|July 19, 2012
PubMed
Summary

Short peptides stimulate differentiation factors in aging human cells. These peptides, including pancragen, bronchogen, and vesugen, show a geroprotective effect by enhancing cell differentiation markers.

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Peptides from Phage Display Library Modulate Gene Expression in Mesenchymal Cells and Potentiate Osteogenesis in Unicortical Bone Defects
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Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans
10:10

Preparation and Culture of Myogenic Precursor Cells/Primary Myoblasts from Skeletal Muscle of Adult and Aged Humans

Published on: February 16, 2017

Area of Science:

  • Cell biology
  • Molecular biology
  • Gerontology

Background:

  • Cellular aging leads to reduced expression of key differentiation markers.
  • Understanding the molecular mechanisms of aging is crucial for developing interventions.

Purpose of the Study:

  • To investigate the effect of short peptides on differentiation factors in aging human cells.
  • To explore the potential geroprotective mechanisms of these peptides.

Main Methods:

  • Culturing human embryonic pancreatic, bronchial, and prostatic fibroblast cells.
  • Analyzing the expression of differentiation factors (CXCL12, Hoxa3, WEGC1) using quantitative methods.
  • Treating cell cultures with specific peptides (pancragen, bronchogen, vesugen) and assessing their impact on marker expression.

Main Results:

  • Reduced expression of differentiation markers (CXCL12, Hoxa3, WEGC1) was observed in late-passage (aging) cell cultures.
  • Tissue-specific peptides (pancragen, bronchogen, vesugen) stimulated the expression of these differentiation factors.
  • The peptide-induced stimulation was more pronounced in aged cultures, suggesting a geroprotective effect.

Conclusions:

  • Short peptides can effectively stimulate the expression of crucial differentiation factors in human cells.
  • These peptides demonstrate a potential geroprotective effect, particularly in aged cells, by counteracting age-related declines in differentiation markers.