Targeting MAP3K19 prevents human lung myofibroblast activation both in vitro and in a humanized SCID model of idiopathic pulmonary fibrosis.
Isabelle C JonesMilena S EspindolaRohan NarayananAna L CoelhoDavid M HabielStefen A BoehmeTai Wei LyKevin B BaconCory M HogaboamPublished in: Scientific reports (2019)
Idiopathic Pulmonary Fibrosis (IPF) is a disease with a devastating prognosis characterized by unrelenting lung scarring. Aberrant activation of lung fibroblasts is a key feature of this disease, yet the key pathways responsible for this are poorly understood. Mitogen-activated protein kinase, kinase, kinase- 19 (MAP3K19) was recently shown to be upregulated in IPF and this MAPK has a key role in target gene transcription in the TGF-β pathway. Herein, we further investigate the role of MAP3K19 in cultured normal and IPF fibroblasts and in a humanized SCID mouse model of IPF employing both short interfering (si) RNA and novel small-molecule inhibitors directed at this kinase. Targeting MAP3K19 had significant inhibitory effects on the expression of both alpha smooth muscle actin and extracellular matrix in cultured human IPF fibroblasts. Quantitative protein and biochemical assays, as well as histological analysis, showed that MAP3K19 was required for the development of lung fibrosis in SCID mice humanized with IPF lung fibroblasts. MAP3K19 was required for IPF myofibroblast differentiation, and targeting its activity attenuated the profibrotic activity of these cells both in vitro and in an adoptive transfer SCID model of pulmonary fibrosis.
Keyphrases
- idiopathic pulmonary fibrosis
- extracellular matrix
- pulmonary fibrosis
- interstitial lung disease
- small molecule
- endothelial cells
- high density
- smooth muscle
- mouse model
- protein kinase
- transforming growth factor
- tyrosine kinase
- cancer therapy
- poor prognosis
- signaling pathway
- genome wide
- long non coding rna
- gene expression
- binding protein
- adipose tissue
- dna methylation
- cell proliferation
- mesenchymal stem cells
- deep learning
- cell death
- amino acid
- cell cycle arrest
- transcription factor