In:
Journal of Cellular Biochemistry, Wiley, Vol. 113, No. 12 ( 2012-12), p. 3797-3809
Abstract:
Regulatory T cells (Tregs) are critical for maintaining self‐tolerance and homeostasis, and have potential application in clinical disease therapy, such as autoimmune diseases and transplant rejection, but their numbers are limited. FOXP3 is a key transcription factor controlling Tregs development and function. Although transfection of CD4 + CD25 − lymphocytes with the FOXP3 gene can convert them to Treg‐like cells, there is the risk of insertional mutagenesis and thus an alternative to genetic intervention is sought. The protein transduction domain (PTD) from the HIV transactivator of transcription is a useful tool to deliver protein to the cytoplasm and nucleus. In this study, we generated a fusion protein linking the human FOXP3 to PTD (PTD‐hFOXP3), and explored its function in T cells. The results showed that the PTD rapidly and effectively delivered the hFOXP3 protein into cells where it localized not only in the cytoplasm, but also to the nucleus. PTD‐hFOXP3‐transduced Jurkat cells (human T lymphoma cell line) and CD4 + CD25 − T cells failed to proliferate and produce IL‐2 and IFN‐γ, but produced large amounts of the cytokines IL‐4, IL‐10, and TGF‐β, in response to TCR stimulation in vitro. PTD‐hFOXP3‐transduced CD4 + CD25 − T cells also expressed high levels of CTLA‐4 and low levels of CD25 after stimulation. Most importantly, PTD‐hFOXP3‐transduced T cells inhibited the proliferation of activated CD4 + CD25 − T cells. Furthermore, chromatin immunoprecipitation assays demonstrated that PTD‐hFOXP3 can bind with the IL‐2 gene promoter and repress the expression of IL‐2. These results indicate that PTD‐hFOXP3 has the capability to convert conventional T cells to Treg‐like cells. J. Cell. Biochem. 113: 3797–3809, 2012. © 2012 Wiley Periodicals, Inc.
Type of Medium:
Online Resource
ISSN:
0730-2312
,
1097-4644
Language:
English
Publisher:
Wiley
Publication Date:
2012
detail.hit.zdb_id:
1479976-5
SSG:
12
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