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. 2018 Feb 5;5:10. doi: 10.3389/fmed.2018.00010

Table 1.

Mitochondrial changes in the fibrotic lung.

Feature Change Model Reference
Mitochondrial reactive oxygen species Increased Bleomycin mouse model (44)
Asbestosis mouse model

Mitochondrial respiration Decreased ETC complex activity, lower OCR Human idiopathic pulmonary fibrosis (IPF) lung tissue (5, 15, 42, 43, 63, 66, 69)
Human lung fibroblasts
Human AECII
Alveolar macrophages
MHV68 model of lung fibrosis

ATP production Decreased IPF lung fibroblasts (24, 43, 69)
IPF lung myofibroblasts
IPF total lung

mtDNA Increased oxidative damage, insufficient mtDNA repair IPF total lung (5, 44, 48)
Murine AECII
Bleomycin mouse model
Asbestosis mouse model

Mitochondrial biogenesis Decrease IPF total lung (15)
Bleomycin mouse model
Mitochondrial dynamics Imbalanced MHV68 mouse model of fibrosis (5)

Mitophagy alterations Reduced levels of mediators of mitochondrial quality control in epithelial cells and fibroblasts IPF AECII
IPF lung fibroblasts
IPF pulmonary macrophages
Bleomycin mouse model
(5, 24, 25, 30)
Increased mitophagy in macrophages
MHV68 mouse model of fibrosis

Decreased expression of SIRT3 Acetylation of mitochondrial proteins IPF total lung (48, 52)
Bleomycin mouse model
Asbestosis mouse model

ETC, electron transport chain; OXPHOS, oxidative phosphorylation; AECII, alveolar type II epithelial cells; OCR, oxygen consumption rate.