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Identifying Foxp3-expressing suppressor T cells with a bicistronic reporter.

http://www.ncbi.nlm.nih.gov/pubmed/15795373

Regulatory T cells are critical for maintaining self-tolerance and to negatively regulate immune responses. Foxp3 is a regulatory T cell-specific transcription factor that functions as the master regulator of the development and function of regulatory T cells. Here, we report the generation of a mouse model, in which a bicistronic reporter expressing a red fluorescent protein has been knocked into the endogenous Foxp3 locus. Using this mouse model, we assessed Foxp3 expression in various lymphocyte compartments and identified previously unreported Foxp3-expressing cells. In addition, we showed that de novo Foxp3 expression along with suppressive function were induced by TGF-beta in activated CD4 T cells in vitro. Finally, we demonstrated that non-Foxp3-expressing CD4 T cells could not be converted into Foxp3-expressing cells upon adoptive transfer into immunodeficient hosts. This Foxp3 bicistronic reporter knockin mouse model should greatly enhance the study of regulation and function of Foxp3-expressing regulatory T cells.

Pubmed ID: 15795373 RIS Download

Mesh terms: Adoptive Transfer | Animals | Base Sequence | DNA | DNA-Binding Proteins | Forkhead Transcription Factors | Gene Expression | Genes, Reporter | In Vitro Techniques | Luminescent Proteins | Mice | Mice, Inbred BALB C | Mice, Inbred C57BL | Mice, Knockout | Mice, Transgenic | Models, Animal | Models, Immunological | Recombinant Proteins | Severe Combined Immunodeficiency | T-Lymphocytes, Regulatory | Transforming Growth Factor beta

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Associated grants

  • Agency: NIDDK NIH HHS, Id: R01 DK51665

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