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The Journal of Immunology, 2000, 164: 5782-5787.
Copyright © 2000 by The American Association of Immunologists

Size Estimate of the {alpha}ß TCR Repertoire of Naive Mouse Splenocytes1

Armanda Casrouge*, Emmanuel Beaudoing{dagger}, Sophie Dalle*, Christophe Pannetier*, Jean Kanellopoulos2,* and Philippe Kourilsky*

* Unité de Biologie Moléculaire du Gène, Institut National de la Santé et de la Recherche Médicale, Unité 277, Institut Pasteur, Paris, France; and {dagger} Information Génétique et Structurale, EP 91, Centre National de la Recherche Scientifique, Institut de Biologie Structurale et Microbiologie, Marseille, France

The diversity of the T cell repertoire of mature T splenocytes is generated, in the thymus, by pairing of {alpha} and ß variable domains of the {alpha}ß TCR and by the rearrangements of various gene segments encoding these domains. In the periphery, it results from competition between various T cell subpopulations including recent thymic migrants and long-lived T cells. Quantitative data on the actual size of the T cell repertoire are lacking. Using PCR methods and extensive sequencing, we have measured for the first time the size of the TCR-{alpha}ß repertoire of naive mouse T splenocytes. There are 5–8 x 105 different nucleotide sequences of BV chains in the whole spleen of young adult mice. We have also determined the size of the BV repertoire in a subpopulation of AV2+ T splenocytes, which allows us to provide a minimum estimate of the {alpha}ß repertoire. We find that the mouse spleen harbors about 2 x 106 clones of about 10 cells each. This figure, although orders of magnitude smaller than the maximum theoretical diversity (estimated up to 1015), is still large enough to maintain a high functional diversity.




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