Brg1 aggravates airway inflammation in asthma via inhibition of the PI3K/Akt/mTOR pathway

Biochem Biophys Res Commun. 2018 Sep 18;503(4):3212-3218. doi: 10.1016/j.bbrc.2018.08.127. Epub 2018 Aug 24.

Abstract

The PI3K/Akt/mTOR pathway is thought to be closely associated with airway inflammation and is regulated by various upstream proteins. Brahma-related gene 1 (Brg1) plays an important role in chromatin remodeling and facilitates recruitment of essential transcription factors, leading to regulation of gene expression. Thus, the present study aimed at evaluating the anti-inflammatory role of Brg1 on house dust mite (HDM)-induced asthma through regulating the PI3K/Akt/mTOR pathway. The Brgfl/fl mice were crossbred with the SFTPC-Cre mice to generate bronchial epithelial cell specific Brg1 knockout mice, and LY294002 was used to inhibit PI3K. Western blot, immunofluorescence, immunoprecipitation, and immunohistochemical staining were used to detect the expression of proteins. An increase in Brg1 and a decrease in the PI3K/Akt/mTOR pathway activity were detected in asthmatic mice, but not in control mice. When Brg1 was knocked out, the asthma severity was ameliorated and the PI3K/Akt/mTOR pathway was activated. However, this protective effect could be suppressed by LY294002. Additionally, we observed that Brg1 was co-localized and co-immunoprecipitated with PI3K, using immunofluorescence and immunoprecipitation assays. Our results suggest that Brg1 might play an essential role in maintaining airway inflammation and affect the PI3K/Akt/mTOR pathway in asthma.

Keywords: Airway inflammation; Akt; Brg1; PI3K; mTOR.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Asthma / immunology*
  • Asthma / pathology
  • DNA Helicases / immunology*
  • Female
  • Inflammation / immunology
  • Inflammation / pathology
  • Mice, Inbred C57BL
  • Nuclear Proteins / immunology*
  • Phosphatidylinositol 3-Kinases / immunology*
  • Proto-Oncogene Proteins c-akt / immunology*
  • Signal Transduction*
  • TOR Serine-Threonine Kinases / immunology*
  • Transcription Factors / immunology*

Substances

  • Nuclear Proteins
  • Transcription Factors
  • mTOR protein, mouse
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • Smarca4 protein, mouse
  • DNA Helicases