Mcl-1 protects eosinophils from apoptosis and exacerbates allergic airway inflammation

Thorax. 2020 Jul;75(7):600-605. doi: 10.1136/thoraxjnl-2019-213204. Epub 2020 Apr 17.

Abstract

Eosinophils are key effector cells in allergic diseases. Here we investigated Mcl-1 (an anti-apoptotic protein) in experimental allergic airway inflammation using transgenic overexpressing human Mcl-1 mice (hMcl-1) and reducing Mcl-1 by a cyclin-dependent kinase inhibitor. Overexpression of Mcl-1 exacerbated allergic airway inflammation, with increased bronchoalveolar lavage fluid cellularity, eosinophil numbers and total protein, and an increase in airway mucus production. Eosinophil apoptosis was suppressed by Mcl-1 overexpression, with this resistance to apoptosis attenuated by cyclin-dependent kinase inhibition which also rescued Mcl-1-exacerbated allergic airway inflammation. We propose that targeting Mcl-1 may be beneficial in treatment of allergic airway disease.

Keywords: allergic lung disease; asthma mechanisms; eosinophil biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis
  • Asthma / genetics*
  • Asthma / metabolism
  • Asthma / pathology
  • Bronchoalveolar Lavage Fluid
  • Disease Models, Animal
  • Eosinophils / metabolism
  • Eosinophils / pathology*
  • Female
  • Gene Expression Regulation*
  • Hypersensitivity / genetics*
  • Hypersensitivity / metabolism
  • Hypersensitivity / pathology
  • Leukocyte Count
  • Mice
  • Mice, Transgenic
  • Myeloid Cell Leukemia Sequence 1 Protein / biosynthesis
  • Myeloid Cell Leukemia Sequence 1 Protein / genetics*
  • RNA / genetics*

Substances

  • Mcl1 protein, mouse
  • Myeloid Cell Leukemia Sequence 1 Protein
  • RNA