Subcellular localization of FOXP3 in human regulatory and nonregulatory T cells

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Abstract

The transcriptional regulator FOXP3 is an important determinant of regulatory T (Treg) cell development and function and is frequently used to quantitate Treg cells. However, FOXP3 is also expressed in recently activated conventional human T cells. Here, we investigated the FOXP3 expression patterns in Treg and activated T cells at a cellular level. Upon activation, human CD4 +CD25 - T cells expressed FOXP3 mainly in the cytoplasm, in sharp contrast to human CD4 +CD25 + Treg cells, where we found FOXP3 to be predominantly expressed in the nucleus. A GFP-FOXP3-fusion protein shuttled from the nucleus to the cytoplasm in transfected primary human T cells. We identified two novel leucine-rich nuclear export signals in FOXP3. Site-directed mutagenesis of both sequences completely abolished nuclear export of FOXP3 in human T cells. Both export sequences localized to exons affected by alternative splicing. The three isoforms FOXP3Δ2, FOXP3Δ7, and FOXP3Δ2Δ7 localized preferentially to the nucleus. Additionally, forced expression of nucleus-directed FOXP3 induced a Treg-cell-associated gene expression pattern and induced regulatory capacity. These findings should aid in the interpretation of future studies utilizing FOXP3 expression as a Treg-cell marker and shed some light on the molecular mechanisms controlling subcellular FOXP3 localization in human T cells. © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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Magg, T., Mannert, J., Ellwart, J. W., Schmid, I., & Albert, M. H. (2012). Subcellular localization of FOXP3 in human regulatory and nonregulatory T cells. European Journal of Immunology, 42(6), 1627–1638. https://doi.org/10.1002/eji.201141838

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