Please use this identifier to cite or link to this item: https://doi.org/10.1038/srep00642
Title: In situ differentiation of CD8α αt cells from CD4 T cells in peripheral lymphoid tissues
Authors: Nambu, Y.
Hayashi, T.
Jang, K.-J.
Aoki, K.
Mano, H.
Nakano, K.
Osato, M. 
Takahashi, K.
Itoh, K.
Teramukai, S.
Komori, T.
Fujita, J.
Ito, Y.
Shimizu, A.
Sugai, M.
Issue Date: 2012
Citation: Nambu, Y., Hayashi, T., Jang, K.-J., Aoki, K., Mano, H., Nakano, K., Osato, M., Takahashi, K., Itoh, K., Teramukai, S., Komori, T., Fujita, J., Ito, Y., Shimizu, A., Sugai, M. (2012). In situ differentiation of CD8α αt cells from CD4 T cells in peripheral lymphoid tissues. Scientific Reports 2 : -. ScholarBank@NUS Repository. https://doi.org/10.1038/srep00642
Abstract: Mutually exclusive cell fate determination of CD4 helper or CD8 killer T cells occurs in the thymus. These T-cell subsets are not believed to redirect other lineages. Here we showed that retinoic acid and transforming growth factor-Î 21 promoted the differentiation of CD8α α T cells from CD4 T cells in a Runx3-dependent manner. These cells were inferred to belong to immunoregulatory populations because subpopulations of CD8αα+TCRαβ T cells are known to suppress activated T cells, and mice with Runx3-/-' T cells showed defects during recovery from experimental allergic encephalomyelitis. Our results demonstrate that CD4 T cells play fundamental roles in controlling immune reactions through promotion and attenuation. We accordingly anticipate that clarifying the mechanisms underlying this process will provide insights leading to autoimmune and immunodeficiency disease therapies.
Source Title: Scientific Reports
URI: http://scholarbank.nus.edu.sg/handle/10635/110750
ISSN: 20452322
DOI: 10.1038/srep00642
Appears in Collections:Staff Publications

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