TRIM72 is required for effective repair of alveolar epithelial cell wounding

Am J Physiol Lung Cell Mol Physiol. 2014 Sep 15;307(6):L449-59. doi: 10.1152/ajplung.00172.2014. Epub 2014 Aug 8.

Abstract

The molecular mechanisms for lung cell repair are largely unknown. Previous studies identified tripartite motif protein 72 (TRIM72) from striated muscle and linked its function to tissue repair. In this study, we characterized TRIM72 expression in lung tissues and investigated the role of TRIM72 in repair of alveolar epithelial cells. In vivo injury of lung cells was introduced by high tidal volume ventilation, and repair-defective cells were labeled with postinjury administration of propidium iodide. Primary alveolar epithelial cells were isolated and membrane wounding and repair were labeled separately. Our results show that absence of TRIM72 increases susceptibility to deformation-induced lung injury whereas TRIM72 overexpression is protective. In vitro cell wounding assay revealed that TRIM72 protects alveolar epithelial cells through promoting repair rather than increasing resistance to injury. The repair function of TRIM72 in lung cells is further linked to caveolin 1. These data suggest an essential role for TRIM72 in repair of alveolar epithelial cells under plasma membrane stress failure.

Keywords: acute lung injury; alveolar epithelial cells; caveolin 1; plasma membrane wounding and repair; tripartite motif protein 72.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Caveolin 1 / genetics
  • Caveolin 1 / metabolism
  • Cell Membrane / genetics
  • Cell Membrane / metabolism*
  • Cell Membrane / pathology*
  • Cells, Cultured
  • Epithelial Cells* / metabolism
  • Epithelial Cells* / pathology
  • Membrane Proteins
  • Mice
  • Mice, Knockout
  • Pulmonary Alveoli* / injuries
  • Pulmonary Alveoli* / metabolism
  • Pulmonary Alveoli* / pathology
  • Wound Healing*

Substances

  • Carrier Proteins
  • Cav1 protein, mouse
  • Caveolin 1
  • MG53 protein, mouse
  • Membrane Proteins