Receptor for Advanced Glycation End-products Regulates Lung Fluid Balance Via Protein Kinase C-gp91(phox) Signaling to Epithelial Sodium Channels
Overview
Molecular Biology
Affiliations
The receptor for advanced glycation end-products (RAGE), a multiligand member of the Ig family, may play a crucial role in the regulation of lung fluid balance. We quantified soluble RAGE (sRAGE), a decoy isoform, and advanced glycation end-products (AGEs) from the bronchoalveolar lavage fluid of smokers and nonsmokers, and tested the hypothesis that AGEs regulate lung fluid balance through protein kinase C (PKC)-gp91(phox) signaling to the epithelial sodium channel (ENaC). Human bronchoalveolar lavage samples from smokers showed increased AGEs (9.02 ± 3.03 μg versus 2.48 ± 0.53 μg), lower sRAGE (1,205 ± 292 pg/ml versus 1,910 ± 263 pg/ml), and lower volume(s) of epithelial lining fluid (97 ± 14 ml versus 133 ± 17 ml). sRAGE levels did not predict ELF volumes in nonsmokers; however, in smokers, higher volumes of ELF were predicted with higher levels of sRAGE. Single-channel patch clamp analysis of rat alveolar epithelial type 1 cells showed that AGEs increased ENaC activity measured as the product of the number of channels (N) and the open probability (Po) (NPo) from 0.19 ± 0.08 to 0.83 ± 0.22 (P = 0.017) and the subsequent addition of 4-hydroxy-2, 2, 6, 6-tetramethylpiperidine-N-oxyl decreased ENaC NPo to 0.15 ± 0.07 (P = 0.01). In type 2 cells, human AGEs increased ENaC NPo from 0.12 ± 0.05 to 0.53 ± 0.16 (P = 0.025) and the addition of 4-hydroxy-2, 2, 6, 6-tetramethylpiperidine-N-oxyl decreased ENaC NPo to 0.10 ± 0.03 (P = 0.013). Using molecular and biochemical techniques, we observed that inhibition of RAGE and PKC activity attenuated AGE-induced activation of ENaC. AGEs induced phosphorylation of p47(phox) and increased gp91(phox)-dependent reactive oxygen species production, a response that was abrogated with RAGE or PKC inhibition. Finally, tracheal instillation of AGEs promoted clearance of lung fluid, whereas concomitant inhibition of RAGE, PKC, and gp91(phox) abrogated the response.
Hsieh P, Yu C, Chu P, Hsieh P Antioxidants (Basel). 2021; 10(9).
PMID: 34573077 PMC: 8464661. DOI: 10.3390/antiox10091445.
Response of the ileum transcriptome to probiotic and fructo-oligosaccharides in Taiping chicken.
Luo L, Ma F, Wang Q J Appl Genet. 2021; 62(2):307-317.
PMID: 33638812 DOI: 10.1007/s13353-021-00624-5.
Redox Signaling and Advanced Glycation Endproducts (AGEs) in Diet-Related Diseases.
Cepas V, Collino M, Mayo J, Sainz R Antioxidants (Basel). 2020; 9(2).
PMID: 32041293 PMC: 7070562. DOI: 10.3390/antiox9020142.
Grant G, Liou T, Paine 3rd R, Helms M Am J Physiol Cell Physiol. 2020; 318(3):C570-C580.
PMID: 31913693 PMC: 7099525. DOI: 10.1152/ajpcell.00291.2019.
HMGB1 Mediates Paraquat-Induced Neuroinflammatory Responses via Activating RAGE Signaling Pathway.
Huang M, Guo M, Wang K, Wu K, Li Y, Tian T Neurotox Res. 2019; 37(4):913-925.
PMID: 31858421 DOI: 10.1007/s12640-019-00148-1.