New Therapeutic Options in Pulmonal Diseases: Sphingolipids and Modulation of Sphingolipid Metabolism
- PMID: 37922034
- DOI: 10.1007/164_2023_700
New Therapeutic Options in Pulmonal Diseases: Sphingolipids and Modulation of Sphingolipid Metabolism
Abstract
Sphingolipids are crucial molecules in the respiratory airways. As in most other tissues and organs, in the lung sphingolipids play an essential role as structural constituents as they regulate barrier function and fluidity of cell membranes. A lung-specific feature is the occurrence of sphingolipids as minor structural components in the surfactant. However, sphingolipids are also key signaling molecules involved in airway cell signaling and their dynamical formation and metabolism are important for normal lung physiology. Dysregulation of sphingolipid metabolism and signaling is involved in altering lung tissue and initiates inflammatory processes promoting the pathogenesis of pulmonal diseases including cystic fibrosis (CF), chronic obstructive pulmonary disease (COPD), and asthma.In the present review, the important role of specific sphingolipid species in pulmonal diseases will be discussed. Only such an understanding opens up the possibility of developing new therapeutic strategies with the aim of correcting the imbalance in sphingolipid metabolism and signaling. Such delivery strategies have already been studied in animal models of these lung diseases, demonstrating that targeting the sphingolipid profile represents new therapeutic opportunities for lung disorders.
Keywords: Asthma bronchiale; COPD; Ceramides; Cystic fibrosis; Sphingolipids; Sphingosine; Sphingosine 1-phosphate.
© 2023. The Author(s), under exclusive license to Springer Nature Switzerland AG.
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References
-
- Adams C, Icheva V, Deppisch C, Lauer J, Herrmann G, Graepler-Mainka U, Heyder S, Gulbins E, Riethmueller J (2016) Long-term Pulmonal therapy of cystic fibrosis-patients with amitriptyline. Cell Physiol Biochem 39:565–572. https://doi.org/10.1159/000445648 - DOI - PubMed
-
- Barrera NP, Zhou M, Robinson CV (2013) The role of lipids in defining membrane protein interactions: insights from mass spectrometry. Trends Cell Biol 23:1–8. https://doi.org/10.1016/j.tcb.2012.08.007 - DOI - PubMed
-
- Becker KA, Riethmuller J, Luth A, Doring G, Kleuser B, Gulbins E (2010) Acid sphingomyelinase inhibitors normalize pulmonary ceramide and inflammation in cystic fibrosis. Am J Respir Cell Mol Biol 42:716–724. https://doi.org/10.1165/rcmb.2009-0174OC - DOI - PubMed
-
- Becker KA, Verhaegh R, Verhasselt HL, Keitsch S, Soddemann M, Wilker B, Wilson GC, Buer J, Ahmad SA, Edwards MJ, Gulbins E (2021) Acid ceramidase rescues cystic fibrosis mice from pulmonary infections. Infect Immun 89. https://doi.org/10.1128/IAI.00677-20
-
- Bektas M, Allende ML, Lee BG, Chen W, Amar MJ, Remaley AT, Saba JD, Proia RL (2010) Sphingosine 1-phosphate lyase deficiency disrupts lipid homeostasis in liver. J Biol Chem 285:10880–10889. https://doi.org/10.1074/jbc.M109.081489 - DOI - PubMed - PMC
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