Epigenetic regulation of the expression of Il12 and Il23 and autoimmune inflammation by the deubiquitinase Trabid
Sun and colleagues show that the deubiquitinase Trabid mediates the TLR-induced deubiqutination and stabilization of the histone demethylase Jmjd2d at the Il12 and Il23 promoters in dendritic cells. The proinflammatory cytokines interleukin 12 (IL-12) and IL-23 connect innate responses and adaptive...
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Published in | Nature immunology Vol. 17; no. 3; pp. 259 - 268 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.03.2016
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Sun and colleagues show that the deubiquitinase Trabid mediates the TLR-induced deubiqutination and stabilization of the histone demethylase Jmjd2d at the
Il12
and
Il23
promoters in dendritic cells.
The proinflammatory cytokines interleukin 12 (IL-12) and IL-23 connect innate responses and adaptive immune responses and are also involved in autoimmune and inflammatory diseases. Here we describe an epigenetic mechanism for regulation of the genes encoding IL-12 (
Il12a
and
Il12b
; collectively called '
Il12
' here) and IL-23 (
Il23a
and
Il12b
; collectively called '
Il23
' here) involving the deubiquitinase Trabid. Deletion of
Zranb1
(which encodes Trabid) in dendritic cells inhibited induction of the expression of
Il12
and
Il23
by Toll-like receptors (TLRs), which impaired the differentiation of inflammatory T cells and protected mice from autoimmune inflammation. Trabid facilitated TLR-induced histone modifications at the promoters of
Il12
and
Il23
, which involved deubiqutination and stabilization of the histone demethylase Jmjd2d. Our findings highlight an epigenetic mechanism for the regulation of
Il12
and
Il23
and establish Trabid as an innate immunological regulator of inflammatory T cell responses. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 ObjectType-Feature-2 content type line 23 |
ISSN: | 1529-2908 1529-2916 1529-2916 |
DOI: | 10.1038/ni.3347 |