ReviewFrontiers in pharmacology2026
Lipid metabolism as a cell-state determinant in pulmonary fibrosis: from epithelial failure to ferroptosis-driven amplification.
Review in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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7 authors.
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Abstract
Despite 2 decades of mechanistic progress, pulmonary fibrosis still progresses in many patients, and established scar rarely resolves. Lipid metabolism has emerged as a unifying lens on this disease, but a useful synthesis requires recognizing that the relevant abnormalities are compartment-specific, stage-dependent, and unevenly supported by human evidence. Here we argue that lipid metabolism in pulmonary fibrosis is best understood as a determinant of cell-state stability, and that its failure plays out differently across three compartments. In alveolar epithelial cells, reduced lipogenesis, impaired fatty-acid oxidation, surfactant imbalance, and lipotoxic stress destabilize the regenerative AT2 state. This compartment exhibits the most consistent correlative human tissue associations reported to date. In fibroblasts, a shift away from fatty-acid oxidation toward anabolic and lipogenic programs likely stabilizes cells into a persistent myofibroblast identity at the expense of more reparative lipofibroblast-like states. In macrophages, altered lipid uptake, oxidized-lipid responses, and disturbed cholesterol handling support a profibrotic niche, with ontogeny and metabolic profile increasingly displacing classical M1/M2 categories. These compartment-specific programs converge on a shared downstream amplifier, namely phospholipid peroxidation and ferroptosis, where the strongest evidence again concerns injured epithelium. Therapeutic strategies group naturally into three tiers: clinical anchors with indirect metabolic relevance, including pirfenidone, nintedanib, and PDE4B inhibition; repurposed agents with metabolic rationale, including metformin, ezetimibe, and PPAR and LXR modulators; and mechanism-driven, largely preclinical strategies targeting mitochondrial-redox balance and ferroptosis. Reframing lipid metabolism as a cell-state determinant clarifies which abnormalities are actionable, in which compartments they matter, and when intervention is most likely to alter disease course.
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