Green Alga Ulva spp. Hydrolysates and Their Peptide Fractions Regulate Cytokine Production in Splenic Macrophages and Lymphocytes Involving the TLR4-NFκB/MAPK Pathways.
Raúl E CianCristina Hernández-ChirlaqueReyes Gámez-BelmonteSilvina R DragoFermín Sánchez de MedinaOlga Martínez-AugustinPublished in: Marine drugs (2018)
Hydrolysates of food protein sources have immunomodulatory effects, which are of interest for use as functional foods. In this study, we have characterized the immune regulatory effect on rat splenocytes, macrophages and T lymphocytes of Ulva spp. hydrolysates and their peptide fractions with or without in vitro gastrointestinal digestion and/or ultrafiltration. IL-10 was induced in almost all conditions and cell types obtained from wild type animals. The induction was in general increased by ultrafiltration and in vitro gastrointestinal digestion. TNF was also induced in basal conditions. In turn, TNF and IFN-γ production was attenuated by the hydrolysate products in lipopolysaccharide or concanavalin A immune stimulated cells. Inhibitors for the activation of NFκB, MAPK p38 and JNK inhibited IL-10 induction in rat splenocytes. The response was dramatically attenuated in TLR4-/- cells, and only modestly in TLR2-/- cells. Food peptides from Ulva spp. genus exert anti-inflammatory effects in immune cells mediated by TLR4 and NFκB. Similarity with the immunomodulatory profile of protein hydrolysates from other sources suggests a common mechanism.
Keyphrases
- induced apoptosis
- signaling pathway
- oxidative stress
- toll like receptor
- pi k akt
- inflammatory response
- cell cycle arrest
- nuclear factor
- lps induced
- immune response
- endoplasmic reticulum stress
- diabetic rats
- rheumatoid arthritis
- high glucose
- wild type
- drinking water
- amino acid
- single cell
- binding protein
- drug induced
- cell proliferation
- risk assessment
- cell therapy
- human health
- climate change