Role of GADD45a in murine models of radiation- and bleomycin-induced lung injury

Am J Physiol Lung Cell Mol Physiol. 2015 Dec 15;309(12):L1420-9. doi: 10.1152/ajplung.00146.2014. Epub 2015 Oct 23.

Abstract

We previously reported protective effects of GADD45a (growth arrest and DNA damage-inducible gene 45 alpha) in murine ventilator-induced lung injury (VILI) via effects on Akt-mediated endothelial cell signaling. In the present study we investigated the role of GADD45a in separate murine models of radiation- and bleomycin-induced lung injury. Initial studies of wild-type mice subjected to single-dose thoracic radiation (10 Gy) confirmed a significant increase in lung GADD45a expression within 24 h and persistent at 6 wk. Mice deficient in GADD45a (GADD45a(-/-)) demonstrated increased susceptibility to radiation-induced lung injury (RILI, 10 Gy) evidenced by increased bronchoalveolar lavage (BAL) fluid total cell counts, protein and albumin levels, and levels of inflammatory cytokines compared with RILI-challenged wild-type animals at 2 and 4 wk. Furthermore, GADD45a(-/-) mice had decreased total and phosphorylated lung Akt levels both at baseline and 6 wk after RILI challenge relative to wild-type mice while increased RILI susceptibility was observed in both Akt(+/-) mice and mice treated with an Akt inhibitor beginning 1 wk prior to irradiation. Additionally, overexpression of a constitutively active Akt1 transgene reversed RILI-susceptibility in GADD45a(-/-) mice. In separate studies, lung fibrotic changes 2 wk after treatment with bleomycin (0.25 U/kg IT) was significantly increased in GADD45a(-/-) mice compared with wild-type mice assessed by lung collagen content and histology. These data implicate GADD45a as an important modulator of lung inflammatory responses across different injury models and highlight GADD45a-mediated signaling as a novel target in inflammatory lung injury clinically.

Keywords: Akt; GADD45a; bleomycin; lung fibrosis; lung injury; radiation pneumonitis.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Bleomycin / adverse effects*
  • Cell Cycle Proteins / metabolism*
  • Collagen / metabolism
  • Disease Models, Animal
  • Female
  • Inflammation / chemically induced
  • Inflammation / metabolism
  • Lung / drug effects
  • Lung / metabolism*
  • Lung / radiation effects
  • Lung Injury / chemically induced*
  • Lung Injury / metabolism*
  • Mice
  • Mice, Inbred C57BL
  • Nuclear Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism
  • Pulmonary Fibrosis / chemically induced
  • Pulmonary Fibrosis / metabolism
  • Radiation
  • Signal Transduction / physiology

Substances

  • Cell Cycle Proteins
  • Gadd45a protein, mouse
  • Nuclear Proteins
  • Bleomycin
  • Collagen
  • Proto-Oncogene Proteins c-akt