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Publication : α-Klotho protects against oxidative damage in pulmonary epithelia.

First Author  Ravikumar P Year  2014
Journal  Am J Physiol Lung Cell Mol Physiol Volume  307
Issue  7 Pages  L566-75
PubMed ID  25063799 Mgi Jnum  J:222072
Mgi Id  MGI:5643918 Doi  10.1152/ajplung.00306.2013
Citation  Ravikumar P, et al. (2014) alpha-Klotho protects against oxidative damage in pulmonary epithelia. Am J Physiol Lung Cell Mol Physiol 307(7):L566-75
abstractText  alpha-Klotho exerts pleiotropic biological actions. Heterozygous alpha-Klotho haplo-insufficient mice (kl/+) appear normal at baseline except for age-related changes in the lung, suggesting heightened pulmonary susceptibility to alpha-Klotho deficiency. We used in vivo and in vitro models to test whether alpha-Klotho protects lung epithelia against injury. Normally, alpha-Klotho is not expressed in the lung, but circulating alpha-Klotho levels are reduced -40% in kl/+ mice and undetectable in homozygous alpha-Klotho-deficient mice (kl/kl). kl/+ mice show distal air space enlargement at a given airway pressure, with elevated lung oxidative damage marker (8-hydroxydeoxyguanosine; 8-OHdG); these abnormalities are exacerbated in kl/kl mice. Studies were performed in A549 lung epithelial cells and/or primary culture of alveolar epithelial cells. Hyperoxia (95% O2) and high inorganic phosphate concentrations (Pi, 3-5 mM) additively caused cell injury (lactate dehydrogenase release), oxidative DNA damage (8-OHdG), lipid oxidation (8-isoprostane), protein oxidation (carbonyl), and apoptosis (caspase-8 activity and TUNEL stain). Transfection of transmembrane or soluble alpha-Klotho, or addition of soluble alpha-Klotho-containing conditioned media, increased cellular antioxidant capacity (Cu- and Fe-based assays) via increased nuclear factor erythroid-derived 2-related factors 1 and 2 (Nrf1/2) transcriptional activity and ameliorated hyperoxic and phosphotoxic injury. To validate the findings in vivo, we injected alpha-Klotho-containing conditioned media into rat peritoneum before and during hyperoxia exposure and found reduced alveolar interstitial edema and oxidative damage. We conclude that circulating alpha-Klotho protects the lung against oxidative damage and apoptosis partly via increasing endogenous antioxidative capacity in pulmonary epithelia. Cytoprotection by alpha-Klotho may play an important role in degenerative diseases of the lung.
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