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Related Concept Videos

The Effect of Aging on Tissues01:19

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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...
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Related Experiment Video

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Quantitative Imaging of Lineage-specific Toll-like Receptor-mediated Signaling in Monocytes and Dendritic Cells from Small Samples of Human Blood
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Alterations in gene array patterns in dendritic cells from aged humans.

Jia-ning Cao1, Anshu Agrawal1, Edward Sharman2

  • 1Division of Basic and Clinical Immunology, Department of Medicine, University of California Irvine, Irvine, California, United States of America.

Plos One
|September 6, 2014
PubMed
Summary
This summary is machine-generated.

Aging impairs dendritic cell (DC) function by altering gene expression. Key immune and cell cycle genes are downregulated in aged DCs, contributing to reduced immunity in older adults.

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Area of Science:

  • Immunology
  • Gerontology
  • Molecular Biology

Background:

  • Dendritic cells (DCs) are crucial antigen-presenting cells regulating immune responses and maintaining tolerance.
  • DC function declines with age, potentially impacting adaptive immunity in the elderly.
  • Understanding these age-related molecular changes is vital for addressing immune senescence.

Purpose of the Study:

  • To identify age-associated molecular alterations in human dendritic cells.
  • To investigate gene expression changes in monocyte-derived DCs (MoDCs) from aged versus young donors.

Main Methods:

  • Gene array analysis using Affymetrix GeneChips.
  • Comparison of gene expression profiles between MoDCs from aged and young human donors.

Main Results:

  • Significant differential expression of 260 genes (1.8%) in aged MoDCs compared to young MoDCs.
  • 144 genes were downregulated and 116 were upregulated.
  • Genes involved in pathogen immune response, cell migration, T cell priming, cell cycle arrest, and DNA replication showed significant age-related changes, with many downregulated by over 3-fold.

Conclusions:

  • Age-associated changes in gene expression provide molecular evidence for functional abnormalities in human DCs.
  • Downregulation of genes related to cell cycle arrest and DNA replication may contribute to genetic instability in aging.
  • These molecular shifts in DCs likely underlie the observed defects in adaptive immunity in the elderly.