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Article: Differential roles of cytokine receptors in the development of epidermal γδ T cells

TitleDifferential roles of cytokine receptors in the development of epidermal γδ T cells
Authors
Issue Date2001
Citation
Journal of Immunology, 2001, v. 167, n. 4, p. 1929-1934 How to Cite?
AbstractIL-7 and IL-15 play important roles in γδ T cell development. These receptors transmit proliferation and/or survival signals in γδ T cells. In addition, the IL-7R promotes recombination and transcription in the TCR γ locus. To clarify the role of the cytokine receptors in the development of epidermal γδ T cells, we introduced a Vγ3/Vδ1 TCR transgene, derived from Thy-1+ dendritic epidermal T cells (DETC), into IL-7Rα-deficient mice, and we found that they partly rescued γδ T cells in the adult thymus but not in the spleen. Introduction of an additional Bcl-2 transgene had a minimal effect on γδ T cells in the adult thymus of these mice. In contrast to the adult thymus, the introduction of the Vγ3/Vδ1 TCR transgene into IL-7Rα-/- mice completely restored Vγ3+ T cells in the fetal thymus and DETC in the adult skin. On the contrary, the same Vγ3/Vδ1 TCR transgene failed to rescue DETC in the skin of IL-2Rβ-deficient mice, even with the additional Bcl-2 transgene. These results suggest that the IL-2/IL-15R, rather than the IL-7R, plays an essential role in proliferation and survival of DETC in the fetal thymus and the skin. In contrast, the IL-7R is probably essential in the induction of V-J recombination of TCRγ, genes. Thus, this study proves that IL-7R and IL-2/IL-15R serve differential functions in epidermal γδ T cell development.
Persistent Identifierhttp://hdl.handle.net/10722/291586
ISSN
2023 Impact Factor: 3.6
2023 SCImago Journal Rankings: 1.558
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorYe, S. K.-
dc.contributor.authorMaki, K.-
dc.contributor.authorLee, H. C.-
dc.contributor.authorIto, A.-
dc.contributor.authorKawai, K.-
dc.contributor.authorSuzuki, H.-
dc.contributor.authorMak, T. W.-
dc.contributor.authorChien, Y. H.-
dc.contributor.authorHonjo, T.-
dc.contributor.authorIkuta, K.-
dc.date.accessioned2020-11-17T14:54:41Z-
dc.date.available2020-11-17T14:54:41Z-
dc.date.issued2001-
dc.identifier.citationJournal of Immunology, 2001, v. 167, n. 4, p. 1929-1934-
dc.identifier.issn0022-1767-
dc.identifier.urihttp://hdl.handle.net/10722/291586-
dc.description.abstractIL-7 and IL-15 play important roles in γδ T cell development. These receptors transmit proliferation and/or survival signals in γδ T cells. In addition, the IL-7R promotes recombination and transcription in the TCR γ locus. To clarify the role of the cytokine receptors in the development of epidermal γδ T cells, we introduced a Vγ3/Vδ1 TCR transgene, derived from Thy-1+ dendritic epidermal T cells (DETC), into IL-7Rα-deficient mice, and we found that they partly rescued γδ T cells in the adult thymus but not in the spleen. Introduction of an additional Bcl-2 transgene had a minimal effect on γδ T cells in the adult thymus of these mice. In contrast to the adult thymus, the introduction of the Vγ3/Vδ1 TCR transgene into IL-7Rα-/- mice completely restored Vγ3+ T cells in the fetal thymus and DETC in the adult skin. On the contrary, the same Vγ3/Vδ1 TCR transgene failed to rescue DETC in the skin of IL-2Rβ-deficient mice, even with the additional Bcl-2 transgene. These results suggest that the IL-2/IL-15R, rather than the IL-7R, plays an essential role in proliferation and survival of DETC in the fetal thymus and the skin. In contrast, the IL-7R is probably essential in the induction of V-J recombination of TCRγ, genes. Thus, this study proves that IL-7R and IL-2/IL-15R serve differential functions in epidermal γδ T cell development.-
dc.languageeng-
dc.relation.ispartofJournal of Immunology-
dc.titleDifferential roles of cytokine receptors in the development of epidermal γδ T cells-
dc.typeArticle-
dc.description.naturelink_to_OA_fulltext-
dc.identifier.doi10.4049/jimmunol.167.4.1929-
dc.identifier.pmid11489972-
dc.identifier.scopuseid_2-s2.0-0035881676-
dc.identifier.volume167-
dc.identifier.issue4-
dc.identifier.spage1929-
dc.identifier.epage1934-
dc.identifier.isiWOS:000170949600014-
dc.identifier.issnl0022-1767-

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