Cell-Intrinsic NF-κB Activation Is Critical for the Development of Natural Regulatory T Cells in Mice

被引:22
|
作者
Gueckel, Eva [1 ]
Frey, Silke [1 ]
Zaiss, Mario M. [2 ]
Schett, Georg [2 ]
Ghosh, Sankar [3 ]
Voll, Reinhard E. [1 ,4 ]
机构
[1] Univ Erlangen Nurnberg, Dept Internal Med, Nikolaus Fiebiger Ctr Mol Med, Clin Res Grp, Erlangen, Germany
[2] Univ Erlangen Nurnberg, Univ Hosp Erlangen, Dept Internal Med Rheumatol & Clin Immunol 3, Erlangen, Germany
[3] Columbia Univ, Coll Phys & Surg, Dept Microbiol & Immunol, New York, NY USA
[4] Univ Med Ctr Freiburg, Dept Rheumatol & Clin Immunol, Ctr Chron Immunodeficiency, Freiburg, Germany
来源
PLOS ONE | 2011年 / 6卷 / 05期
关键词
IMMUNOLOGICAL SELF-TOLERANCE; FOXP3; TRANSCRIPTION-FACTOR; GROWTH-FACTOR-BETA; NUCLEAR-FACTOR; C-REL; IN-VIVO; AUTOIMMUNE ENCEPHALOMYELITIS; DIFFERENTIAL REQUIREMENT; LYMPHOCYTE-PROLIFERATION; INTESTINAL INFLAMMATION;
D O I
10.1371/journal.pone.0020003
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Naturally occurring CD4(+)CD25(+)Foxp3(+) regulatory T (Treg) cells develop in the thymus and represent a mature T cell subpopulation critically involved in maintaining peripheral tolerance. The differentiation of Treg cells in the thymus requires T cell receptor (TCR)/CD28 stimulation along with cytokine-promoted Foxp3 induction. TCR-mediated nuclear factor kappa B (NF-kappa B) activation seems to be involved in differentiation of Treg cells because deletion of components of the NF-kappa B signaling pathway, as well as of NF-kB transcription factors, leads to markedly decreased Treg cell numbers in thymus and periphery. Methodology/ Principal Findings: To investigate if Treg cell-intrinsic NF-kappa B activation is required for thymic development and peripheral homeostasis of Treg cells we used transgenic (Tg) mice with thymocyte-specific expression of a stable I kappa B alpha mutant to inhibit NF-kappa B activation solely within the T cell lineage. Here we show that Treg cell-intrinsic NF-kappa B activation is important for the generation of cytokine-responsive Foxp3(-) thymic Treg precursors and their further differentiation into mature Treg cells. Treg cell development could neither be completely rescued by the addition of exogenous Interleukin 2 (IL-2) nor by the presence of wild-type derived cells in adoptive transfer experiments. However, peripheral NF-kappa B activation appears to be required for IL-2 production by conventional T cells, thereby participating in Treg cell homeostasis. Moreover, pharmacological NF-kappa B inhibition via the I kappa B kinase beta (IKK beta) inhibitor AS602868 led to markedly diminished thymic and peripheral Treg cell frequencies. Conclusion/Significance: Our results indicate that Treg cell-intrinsic NF-kappa B activation is essential for thymic Treg cell differentiation, and further suggest pharmacological NF-kappa B inhibition as a potential therapeutic approach for manipulating this process.
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页数:12
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