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BPTF Is Essential for T Cell Homeostasis and Function
Author(s) -
Bing Wu,
Yunqi Wang,
Chaojun Wang,
Gang Greg Wang,
Jie Wu,
Yisong Y. Wan
Publication year - 2016
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.1600642
Subject(s) - phd finger , bromodomain , transcription factor , chromatin , biology , microbiology and biotechnology , homeostasis , immune system , chromatin remodeling , function (biology) , foxp3 , gene , immunology , epigenetics , genetics , zinc finger
Bromodomain PHD finger transcription factor (BPTF), a ubiquitously expressed ATP-dependent chromatin-remodeling factor, is critical for epigenetically regulating DNA accessibility and gene expression. Although BPTF is important for the development of thymocytes, its function in mature T cells remains largely unknown. By specifically deleting BPTF from late double-negative 3/double-negative 4 stage of developing T cells, we found that BPTF was critical for the homeostasis of T cells via a cell-intrinsic manner. In addition, BPTF was essential for the maintenance and function of regulatory T (Treg) cells. Treg cell-specific BPTF deletion led to reduced Foxp3 expression, increased lymphocyte infiltration in the nonlymphoid organs, and a systemic autoimmune syndrome. These findings therefore reveal a vital role for BPTF in T and Treg cell function and immune homeostasis.

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