p19Arf Exacerbates Cigarette Smoke-Induced Pulmonary Dysfunction

Biomolecules. 2020 Mar 17;10(3):462. doi: 10.3390/biom10030462.

Abstract

Senescent cells accumulate in tissues during aging or pathological settings. The semi-genetic or pharmacological targeting of senescent cells revealed that cellular senescence underlies many aspects of the aging-associated phenotype and diseases. We previously reported that cellular senescence contributes to aging- and disease-associated pulmonary dysfunction. We herein report that the elimination of Arf-expressing cells ameliorates cigarette smoke-induced lung pathologies in mice. Cigarette smoke induced the expression of Ink4a and Arf in lung tissue with concomitant increases in lung tissue compliance and alveolar airspace. The elimination of Arf-expressing cells prior to cigarette smoke exposure protected against these changes. Furthermore, the administration of cigarette smoke extract lead to pulmonary dysfunction, which was ameliorated by subsequent senescent cell elimination. Collectively, these results suggest that senescent cells are a potential therapeutic target for cigarette smoking-associated lung disease.

Keywords: COPD; emphysema; p19Arf; senescence; senolysis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cellular Senescence*
  • Cigarette Smoking / genetics
  • Cigarette Smoking / metabolism*
  • Cigarette Smoking / pathology
  • Cyclin-Dependent Kinase Inhibitor p16 / biosynthesis*
  • Cyclin-Dependent Kinase Inhibitor p16 / genetics
  • Female
  • Lung Diseases / genetics
  • Lung Diseases / metabolism*
  • Lung Diseases / pathology
  • Mice
  • Mice, Transgenic
  • Pulmonary Alveoli / metabolism*
  • Pulmonary Alveoli / pathology

Substances

  • Cdkn2a protein, mouse
  • Cyclin-Dependent Kinase Inhibitor p16