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Cutting Edge: Recombinase-Activating Gene Expression and V(D)J Recombination in CD4+CD3low Mature T Lymphocytes
Author(s) -
Erica Lantelme,
Belinda Palermo,
Luisa Granziero,
Stefania Mantovani,
Rita Campanelli,
V. Monafò,
Antonio Lanzavecchia,
Claudia Giachino
Publication year - 2000
Publication title -
the journal of immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.164.7.3455
Subject(s) - recombinase , v(d)j recombination , germinal center , biology , t cell receptor , gene , rag2 , somatic cell , microbiology and biotechnology , recombination activating gene , receptor , genetics , gene rearrangement , t cell , recombination , b cell , immune system , antibody
The recombinase-activating genes, RAG-1 and RAG-2, can be expressed by a subset of B cells within germinal centers, where they mediate secondary V(D)J rearrangements. This receptor revision mechanism could serve either receptor diversification or tolerance-induced functions. Alternatively, it might rescue those cells the receptors of which have been damaged by somatic mutation. Less is known about the occurrence of similar mechanisms in T cells. Here we show that mature T cells with defective TCR surface expression can express RAG genes and are capable of initiating secondary V(D)J rearrangements. The possibility that a cell rescue mechanism based on the generation of a novel Ag receptor might be active in peripheral T cells is envisaged.

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