期刊
NATURE IMMUNOLOGY
卷 8, 期 4, 页码 359-368出版社
NATURE PUBLISHING GROUP
DOI: 10.1038/ni1445
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- NIAID NIH HHS [R01 AI47154, 2R01 AI065617, R01 AI047154] Funding Source: Medline
Although the development of regulatory T cells ( T-reg cells) in the thymus is defined by expression of the lineage marker Foxp3, the precise function of Foxp3 in T-reg cell lineage commitment is unknown. Here we examined T-reg cell development and function in mice with a Foxp3 allele that directs expression of a nonfunctional fusion protein of Foxp3 and enhanced green fluorescent protein ( Foxp3(Delta EGFP)). Thymocyte development in Foxp3(Delta EGFP) male mice and Foxp3(Delta EGFP/+) female mice recapitulated that of wild-type mice. Although mature EGFP(+) CD4(+) T cells from Foxp3(Delta EGFP) mice lacked suppressor function, they maintained the characteristic T-reg cell 'genetic signature' and failed to develop from EGFP(-) CD4(+) T cells when transferred into lymphopenic hosts, indicative of their common ontogeny with T-reg cells. Our results indicate that T-reg cell effector function but not lineage commitment requires the expression of functional Foxp3 protein.
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