Respiratory syncytial virus potentiates ABCA3 mutation-induced loss of lung epithelial cell differentiation

Hum Mol Genet. 2012 Jun 15;21(12):2793-806. doi: 10.1093/hmg/dds107. Epub 2012 Mar 20.

Abstract

ATP-binding cassette transporter A3 (ABCA3) is a lipid transporter active in lung alveolar epithelial type II cells (ATII) and is essential for their function as surfactant-producing cells. ABCA3 mutational defects cause respiratory distress in newborns and interstitial lung disease (ILD) in children. The molecular pathomechanisms are largely unknown; however, viral infections may initiate or aggravate ILDs. Here, we investigated the impact of the clinically relevant ABCA3 mutations, p.Q215K and p.E292V, by stable transfection of A549 lung epithelial cells. ABCA3 mutations strongly impaired expression of the ATII differentiation marker SP-C and the key epithelial cell adhesion proteins E-cadherin and zonula occludens-1. Concurrently, cells expressing ABCA3 mutation acquired mesenchymal features as observed by increased expression of SNAI1, MMP-2 and TGF-β1, and elevated phosphorylation of Src. Infection with respiratory syncytial virus (RSV), the most common viral respiratory pathogen in small children, potentiated the observed mutational effects on loss of epithelial and acquisition of mesenchymal characteristics. In addition, RSV infection of cells harboring ABCA3 mutations resulted in a morphologic shift to a mesenchymal phenotype. We conclude that ABCA3 mutations, potentiated by RSV infection, induce loss of epithelial cell differentiation in ATII. Loss of key epithelial features may disturb the integrity of the alveolar epithelium, thereby comprising its functionality. We suggest the impairment of epithelial function as a mechanism by which ABCA3 mutations cause ILD.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ATP-Binding Cassette Transporters / genetics*
  • ATP-Binding Cassette Transporters / metabolism
  • Blotting, Western
  • Cadherins / genetics
  • Cadherins / metabolism
  • Cell Differentiation / genetics*
  • Cell Line, Tumor
  • Child
  • Epithelial Cells / metabolism*
  • Epithelial Cells / pathology
  • Epithelial Cells / virology*
  • Gene Expression
  • Host-Pathogen Interactions
  • Humans
  • Infant, Newborn
  • Lung / metabolism
  • Lung / pathology
  • Lung / virology
  • Lung Diseases, Interstitial / genetics
  • Lung Diseases, Interstitial / virology
  • Matrix Metalloproteinase 2 / genetics
  • Matrix Metalloproteinase 2 / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism
  • Mesoderm / metabolism
  • Mesoderm / pathology
  • Microscopy, Fluorescence
  • Mutation*
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Pulmonary Alveoli / metabolism
  • Pulmonary Alveoli / pathology
  • Pulmonary Alveoli / virology
  • Pulmonary Surfactant-Associated Protein C / genetics
  • Pulmonary Surfactant-Associated Protein C / metabolism
  • Respiratory Distress Syndrome, Newborn / genetics
  • Respiratory Distress Syndrome, Newborn / virology
  • Respiratory Syncytial Viruses / physiology*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Snail Family Transcription Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transforming Growth Factor beta1 / genetics
  • Transforming Growth Factor beta1 / metabolism
  • Zonula Occludens-1 Protein

Substances

  • ABCA3 protein, human
  • ATP-Binding Cassette Transporters
  • Cadherins
  • Membrane Proteins
  • Phosphoproteins
  • Pulmonary Surfactant-Associated Protein C
  • SFTPC protein, human
  • SNAI1 protein, human
  • Snail Family Transcription Factors
  • TJP1 protein, human
  • Transcription Factors
  • Transforming Growth Factor beta1
  • Zonula Occludens-1 Protein
  • Matrix Metalloproteinase 2