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Fatty acid synthase downregulation contributes to acute lung injury in murine diet-induced obesity
Maria Plataki, LiChao Fan, Elizabeth Sanchez, Ziling Huang, Lisa K. Torres, Mitsuru Imamura, Yizhang Zhu, David E. Cohen, Suzanne M. Cloonan, Augustine M.K. Choi
Maria Plataki, LiChao Fan, Elizabeth Sanchez, Ziling Huang, Lisa K. Torres, Mitsuru Imamura, Yizhang Zhu, David E. Cohen, Suzanne M. Cloonan, Augustine M.K. Choi
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Research Article Pulmonology

Fatty acid synthase downregulation contributes to acute lung injury in murine diet-induced obesity

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Abstract

The prevalence of obesity is rising worldwide, and obese patients constitute a specific population in the intensive care unit. Acute respiratory distress syndrome (ARDS) incidence is increased in obese patients. Exposure of rodents to hyperoxia mimics many of the features of ARDS. In this report, we demonstrate that high-fat diet–induced obesity increases the severity of hyperoxic acute lung injury in mice in part by altering fatty acid synthase (FASN) levels in the lung. Obese mice exposed to hyperoxia had significantly reduced survival and increased lung damage. Transcriptomic analysis of lung homogenates identified Fasn as one of the most significantly altered mitochondria-associated genes in mice receiving a 60% compared with 10% fat diet. FASN protein levels in the lung of high-fat diet mice were lower by immunoblotting and immunohistochemistry. Depletion of FASN in type II alveolar epithelial cells resulted in altered mitochondrial bioenergetics and more severe lung injury with hyperoxic exposure, even upon administration of a 60% fat diet. This is the first study to our knowledge to show that a high-fat diet leads to altered FASN expression in the lung, and that both a high-fat diet and reduced FASN expression in alveolar epithelial cells promote lung injury.

Authors

Maria Plataki, LiChao Fan, Elizabeth Sanchez, Ziling Huang, Lisa K. Torres, Mitsuru Imamura, Yizhang Zhu, David E. Cohen, Suzanne M. Cloonan, Augustine M.K. Choi

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Figure 4

Mice deficient in FASN in alveolar epithelial cells are more susceptible to lung injury after hyperoxic exposure.

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Mice deficient in FASN in alveolar epithelial cells are more susceptible...
(A) Western blot analysis for FASN in lungs from FASNloxp/loxp SftpcCreERT2+/– (FasniΔAEC2) and SftpcCreERT2+/– (control) mice with β-actin loading control (n = 3 per group). (B) Weight (n = 33 for control and n = 34 for FasniΔAEC2 mice, Mann-Whitney U test, *P < 0.05). (C) Bronchoalveolar lavage fluid (BALF) protein levels from FasniΔAEC2 and control mice after 48 hours of exposure to >95% oxygen or room air (mg/mL, n = 8 per group for room air and n = 15 per group for hyperoxia, ANOVA with Tukey’s post hoc correction, ***P < 0.001, *P < 0.05; similar results were obtained from at least 2 independent experiments). (D) BALF IgM levels from FasniΔAEC2 and control mice after 48 hours of exposure to >95% oxygen or room air (ng/mL, n = 8 per group for room air and n = 15 per group for hyperoxia, ANOVA with Tukey’s post hoc correction, ***P < 0.001, *P < 0.05, similar results were obtained from at least 2 independent experiments). (E) BALF lactate dehydrogenase (LDH) levels after 48 hours of hyperoxia or room air (relative value, n = 8 per group for room air and n = 15 per group for hyperoxia, ANOVA with Tukey’s post hoc correction, *P < 0.05, similar results were obtained from at least 2 independent experiments). (F) Representative image of H&E-stained lungs (n = 3 per group for room air and n = 5 per group for hyperoxia; original magnification, ×20). (G) Alveolar epithelial type II (AEC2) cells were isolated from FasniΔAEC2 and control mice, and protein expression was assessed using the Total OXPHOS (ubiquinone oxidoreductase subunit B8 [NDUFB8], succinate dehydrogenase complex iron sulfur subunit B [SDHB], ubiquinol-cytochrome c reductase core protein 2 [UQCRC2], mitochondrially encoded cytochrome c oxidase 1 [MTCO1], ATP synthase subunit alpha [ATP5A]) (top) and the mitochondrial Membrane Integrity antibody cocktail (outer membrane-porin, intermembrane space-cytochrome c, inner membrane-complex VA and complex III core 1, matrix space-cyclophilin D) (bottom). TOM20 expression was used to confirm equivalent protein input (n = 3 per group). (H) Oxygen consumption rate (OCR, left) and extracellular acidification rate (ECAR, right) of isolated AEC2 cells from FASNloxp/loxp SftpcCreERT2+/– (FasniΔAEC2 AEC2) and SftpcCreERT2+/– mice (Control AEC2) exposed to room air or hyperoxia for 48 hours. All data are raw values (similar results were obtained from 2 independent experiments). Data are expressed as mean ± SEM.

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