z-logo
open-access-imgOpen Access
Withasteroid B from D. metel L. regulates immune responses by modulating the JAK/STAT pathway and the IL‐17 + RORγt + /IL‐10 + FoxP3 + ratio
Author(s) -
Su Y.,
Wang Q.,
Yang B.,
Wu L.,
Cheng G.,
Kuang H.
Publication year - 2017
Publication title -
clinical & experimental immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.329
H-Index - 135
eISSN - 1365-2249
pISSN - 0009-9104
DOI - 10.1111/cei.12998
Subject(s) - rar related orphan receptor gamma , stat protein , foxp3 , janus kinase , stat , immune system , orphan receptor , biology , t cell , retinoic acid , immunology , interleukin 17 , stat6 , proinflammatory cytokine , jak stat signaling pathway , cytokine , psoriasis , stat3 , microbiology and biotechnology , interleukin 4 , signal transduction , transcription factor , cell culture , inflammation , tyrosine kinase , biochemistry , genetics , gene
Summary Datura metel L. is a medicinal herb that contains withasteroids and has a wide range of biological activities. We isolated seven withasteroids from the flowers of D. metel L and examined their ability to inhibit immune responses in vitro and in vivo . Among the withasteroids, withasteroid B2 exhibited the strongest inhibitory effect on immune responses comparing B2 with other isolated compounds from D. metel L., including suppressing the differentiation of CD4 + T cells by inhibiting the expression and production of T cell lineage‐specific master regulators and cytokines and directly suppressing the cytokine‐induced Janus kinase/signal transducer and activator of transcription (JAK/STAT) signalling pathways. In the interleukin (IL)‐23‐induced mouse ear model of skin disease, B2 repressed disease development by inhibiting the expression of proinflammatory mediators in murine ear skin. Moreover, B2 affected the maturation of dendritic cells (DCs) in vitro which, in turn, induced T cell differentiation with an increased regulatory T cell (T reg ) phenotype and decreased T helper type 17 (Th17) phenotype. This study provides new evidence that B2 might ameliorate chronic inflammatory skin diseases by suppressing pathogenic CD4 + T cell differentiation and the IL‐17 + retinoic‐acid‐receptor‐related orphan receptor gamma t (RORγt) + /IL‐10 + forkhead box protein 3 (FoxP3) + ratio. These findings suggest that B2 might mediate the therapeutic effects observed in psoriasis patients following treatment with D. metel L.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom