Inflammation negatively regulates FOXP3 and regulatory T-cell function via DBC1.

Abstract:

:Forkhead box P3 (FOXP3)-positive Treg cells are crucial for maintaining immune homeostasis. FOXP3 cooperates with its binding partners to elicit Treg cells' signature and function, but the molecular mechanisms underlying the modulation of the FOXP3 complex remain unclear. Here we report that Deleted in breast cancer 1 (DBC1) is a key subunit of the FOXP3 complex. We found that DBC1 interacts physically with FOXP3, and depletion of DBC1 attenuates FOXP3 degradation in inflammatory conditions. Treg cells from Dbc1-deficient mice were more resistant to inflammation-mediated abrogation of Foxp3 expression and function and delayed the onset and severity of experimental autoimmune encephalomyelitis and colitis in mice. These findings establish a previously unidentified mechanism regulating FOXP3 stability during inflammation and reveal a pathway for potential therapeutic modulation and intervention in inflammatory diseases.

authors

Gao Y,Tang J,Chen W,Li Q,Nie J,Lin F,Wu Q,Chen Z,Gao Z,Fan H,Tsun A,Shen J,Chen G,Liu Z,Lou Z,Olsen NJ,Zheng SG,Li B

doi

10.1073/pnas.1421463112

subject

Has Abstract

pub_date

2015-06-23 00:00:00

pages

E3246-54

issue

25

eissn

0027-8424

issn

1091-6490

pii

1421463112

journal_volume

112

pub_type

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