Eicosanoids in the Innate Immune Response: TLR and Non-TLR Routes
Author(s) -
Yolanda Álvarez,
Isela Valera,
Cristina Municio,
Etzel Hugo,
Francisco Padrón,
Lydia Blanco,
Mario Rodríguez Rodríguez,
Nieves Fernández,
Mariano Sánchez Crespo
Publication year - 2010
Publication title -
mediators of inflammation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.37
H-Index - 97
eISSN - 1466-1861
pISSN - 0962-9351
DOI - 10.1155/2010/201929
Subject(s) - zymosan , innate immune system , immune system , eicosanoid , autocrine signalling , interleukin 10 , biology , microbiology and biotechnology , cytokine , immunology , chemistry , receptor , arachidonic acid , biochemistry , in vitro , enzyme
The variable array of pattern receptor expression in different cells of the innate immune system explains the induction of distinct patterns of arachidonic acid (AA) metabolism. Peptidoglycan and mannan were strong stimuli in neutrophils, whereas the fungal extract zymosan was the most potent stimulus in monocyte-derived dendritic cells since it induced the production of PGE(2), PGD(2), and several cytokines including a robust IL-10 response. Zymosan activated kappaB-binding activity, but inhibition of NF-kappaB was associated with enhanced IL-10 production. In contrast, treatments acting on CREB (CRE binding protein), including PGE(2), showed a direct correlation between CREB activation and IL-10 production. Therefore, in dendritic cells zymosan induces il10 transcription by a CRE-dependent mechanism that involves autocrine secretion of PGE(2), thus unraveling a functional cooperation between eicosanoid production and cytokine production.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom