Critical Transition in Tissue Homeostasis Accompanies Murine Lung Senescence Impaired Tissue Homeostasis in the Aging Lung
2011

Aging and Lung Health: Understanding Airspace Enlargement in Mice

Sample size: 6 publication 10 minutes Evidence: moderate

Author Information

Author(s): Calvi Carla L., Podowski Megan, D'Alessio Franco R., Metzger Shana L., Misono Kaori, Poonyagariyagorn Hataya, Lopez-Mercado Armando, Ku Therese, Lauer Thomas, Cheadle Christopher, Talbot C. Conover Jr, Jie Chunfa, McGrath-Morrow Sharon, King Landon S., Walston Jeremy, Neptune Enid R.

Primary Institution: Johns Hopkins University School of Medicine

Hypothesis

The study aims to identify molecular signatures of age-related changes in the lung using a murine model.

Conclusion

The study found that early oxidative stress and immune changes precede significant airspace enlargement in aging lungs.

Supporting Evidence

  • Airspace enlargement was observed to begin between 8 and 12 months of age in mice.
  • Increased oxidative stress was noted as a precursor to cell death and airspace enlargement.
  • Immunoglobulin deposition in the lung was significantly increased at 8 and 12 months.
  • B-cell activation was observed during the transition from 8 to 12 months.
  • Macrophage infiltration increased significantly at 12 months of age.

Takeaway

As mice get older, their lungs change in a way that makes them less healthy, and this starts happening earlier than we thought.

Methodology

The study used a murine model to analyze lung changes at various ages through histology, transcriptome analysis, and flow cytometry.

Limitations

The study is limited to a specific mouse strain and may not fully represent human aging.

Participant Demographics

Aged male DBA/2 mice (2–20 months of age)

Statistical Information

P-Value

0.002

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0020712

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