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TCR-α/ß CD4- CD8- double negative T cells arise from CD8+ T cells.
Rodríguez-Rodríguez, Noé; Flores-Mendoza, Giovanna; Apostolidis, Sokratis A; Rosetti, Florencia; Tsokos, George C; Crispín, José C.
Affiliation
  • Rodríguez-Rodríguez N; Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Flores-Mendoza G; Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
  • Apostolidis SA; Current address: Medical Research Council Laboratory of Molecular Biology, Cambridge, UK.
  • Rosetti F; Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico.
  • Tsokos GC; Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, USA.
  • Crispín JC; Current address: Division of Rheumatology, University of Pennsylvania, Philadelphia, Pennsylvania, USA.
J Leukoc Biol ; 108(3): 851-857, 2020 09.
Article in En | MEDLINE | ID: mdl-32052478
ABSTRACT
The cellular origin of CD4- CD8- (double negative, DNT) TCR-α/ß+ T cells remains unknown. Available evidence indicates that they may derive from CD8+ T cells, but most published data have been obtained using cells that bear an invariant transgenic T cell receptor that recognizes an Ag that is not present in normal mice. Here, we have used complementary fate mapping and adoptive transfer experiments to identify the cellular lineage of origin of DNT cells in wild-type mice with a polyclonal T cell repertoire. We show that TCR-α/ß+ DNT cells can be traced back to CD8+ and CD4+ CD8+ double positive cells in the thymus. We also demonstrate that polyclonal DNT cells generated in secondary lymphoid organs proliferate upon adoptive transfer and can regain CD8 expression in lymphopenic environment. These results demonstrate the cellular origin of DNT cells and provide a conceptual framework to understand their presence in pathological circumstances.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: CD4 Antigens / T-Lymphocyte Subsets / Receptors, Antigen, T-Cell, alpha-beta / CD8 Antigens / CD8-Positive T-Lymphocytes / Lymphopoiesis Limits: Animals Language: En Journal: J Leukoc Biol Year: 2020 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: CD4 Antigens / T-Lymphocyte Subsets / Receptors, Antigen, T-Cell, alpha-beta / CD8 Antigens / CD8-Positive T-Lymphocytes / Lymphopoiesis Limits: Animals Language: En Journal: J Leukoc Biol Year: 2020 Document type: Article Affiliation country: