Abstract
The extensive range of specificities of T-cell receptors is generated, as for immunoglobulins, by rearrangement of genetic information1. Much valuable information about rearrangement processes has been inferred by comparing DNA from (monoclonal) lymphoid lines with germ-line DNA2,3 and, for B cells, from rearrangements in some Abelson murine leukaemia virus-transformed cell lines4,5. However, because it is difficult to isolate and grow precursor populations, it has not proved possible to study rearrangements occurring in normal untransformed cells in vitro. Here we show that a single T-cell precursor colonizing an alymphoid thymus lobe in organ culture can generate multiple receptor β-chain gene rearrangements. These observations provide unequivocal evidence for the intra-thymic diversification of the T-cell repertoire. They also offer the possibility of investigating rearrangement and its control in the clonal progeny of a single normal T-cell precursor without the perturbations involved in the use of viral transformation or the production of T-cell hybridomas.
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Williams, G., Kingston, R., Owen, M. et al. A single micromanipulated stem cell gives rise to multiple T-cell receptor gene rearrangements in the thymus in vitro. Nature 324, 63–64 (1986). https://doi.org/10.1038/324063a0
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DOI: https://doi.org/10.1038/324063a0
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