Docosahexaenoic acid reduces suppressive and migratory functions of CD4 + CD25 + regulatory T-cells

AuteurYESSOUFOU, AKADIRI A RACHIDI
AuteurPLE, AUDE
AuteurMOUTAIROU, KABIROU
AuteurHICHAMI, AZIZ
AuteurKHAN, NAIM AKHTAR
Date d'ajout2026-06-02T16:06:57Z
Date de disponibilite2026-06-02T16:06:57Z
Date de publication2009
ResumeImmunological tolerance is one of the fundamental aspects of the immune system. The CD4 + CD25 + regulatory T (Treg) cells have emerged as key players in the development of tolerance to self and foreign antigens. However, little is known about the endogenous factors and mechanisms controlling their suppressive capacity on immune response. In this study, we observed that docosahexaenoic acid (DHA), an n-3 polyunsaturated fatty acid, diminished, in a dose-dependent manner, the capacity of Treg cells to inhibit the CD4 + CD25  effector T-cell proliferation. DHA not only reduced the migration of Treg cells toward chemokines but also downregulated the mRNA expression of CCR-4 and CXCR-4 in Treg cells. DHA also curtailed ERK1/2 and Akt phosphorylation and downregulated the Smad7 levels in these cells. Contradictorily, DHA upregulated the mRNA expression of Foxp3, CTLA-4, TGF-  , and IL-10; nonetheless, this fatty acid increased the expression of p27 KIP1 mRNA, known to be involved in Treg cell unresponsiveness. In Foxp3-immunoprepitated nuclear proteins, DHA upregulated histone desacetylase 7 levels that would again participate in the unresposnsiveness of these cells. Finally, a DHA-enriched diet also diminished, ex vivo, the suppressive capacity of Treg cells. Altogether, these results suggest that DHA, by diminishing Treg cell functions, may play a key role in health and disease
DOI10.1194/jlr.M900101-JLR200
Autre identifiantBECDB-15181
URIhttps://dspace.uac.bj/handle/123456789/12901
Languefr
Fait partie deJournal of Lipid Research
SujetDocosahexaenoic acid reduces suppressive and migratory
Sujetfunctions of Treg cells
TitreDocosahexaenoic acid reduces suppressive and migratory functions of CD4 + CD25 + regulatory T-cells
TypeArticle

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