Anti-inflammatory properties of lemon-derived extracellular vesicles are achieved through the inhibition of ERK/NF-κB signalling pathways

Autor: Stefania Raimondo, Ornella Urzì, Serena Meraviglia, Marta Di Simone, Anna Maria Corsale, Nima Rabienezhad Ganji, Antonio Palumbo Piccionello, Giulia Polito, Elena Lo Presti, Francesco Dieli, Alice Conigliaro, Riccardo Alessandro
Přispěvatelé: Raimondo, Stefania, Urzi, Ornella, Meraviglia, Serena, Di Simone, Marta, Corsale, Anna Maria, Rabienezhad Ganji, Nima, Palumbo Piccionello, Antonio, Polito, Giulia, Lo Presti, Elena, Dieli, Francesco, Conigliaro, Alice, Alessandro, Riccardo
Jazyk: angličtina
Rok vydání: 2022
Předmět:
Popis: Chronic inflammation is associated with the occurrence of several diseases. However, the side effects of anti-inflammatory drugs prompt the identification of new therapeutic strategies. Plant-derived extracellular vesicles (PDEVs) are gaining increasing interest in the scientific community for their biological properties. We isolated PDEVs from the juice of Citrus limon L. (LEVs) and characterized their flavonoid, limonoid and lipid contents through reversed-phase high-performance liquid chromatography coupled to electrospray ionization quadrupole time-of-flight mass spectrometry (RP-HPLC-ESI-Q-TOF-MS). To investigate whether LEVs have a protective role on the inflammatory process, murine and primary human macrophages were pre-treated with LEVs for 24 h and then were stimulated with lipopolysaccharide (LPS). We found that pre-treatment with LEVs decreased gene and protein expression of pro-inflammatory cytokines, such as IL-6, IL1-β and TNF-α, and reduced the nuclear translocation and phosphorylation of NF-κB in LPS-stimulated murine macrophages. The inhibition of NF-κB activation was associated with the reduction in ERK1-2 phosphorylation. Furthermore, the ability of LEVs to decrease pro-inflammatory cytokines and increase anti-inflammatory molecules was confirmed ex vivo in human primary T lymphocytes. In conclusion, we demonstrated that LEVs exert anti-inflammatory effects both in vitro and ex vivo by inhibiting the ERK1-2/NF-κB signalling pathway.
Databáze: OpenAIRE