Common lymphoid progenitors (CLP) are generated in adult bone marrow (BM), but the intermediate steps leading to T cell commitment are unknown, and so is the site at which this commitment occurs. Here, we show that colonies arising in the spleen 12 days after BM injection harbor T cell precursors that are undetectable in BM. These precursors did not generate myeloid cells in vivo but repopulated the thymus and the peripheral T cell compartment much faster than did CLP. Two lineage negative (Lin-) subpopulations were distinguished, namely CD44+ Thy1- cells still capable of natural killer generation and transient low-level B cell generation, and T cell-restricted CD44- Thy1+ cells. At a molecular level, frequency of CD3ε and preTα mRNA was very different in each subset. Furthermore, only the CD44- Thy1+ subset have initiated rearrangements in the T cell receptor β locus. Thus, this study identifies extramedullary T cell progenitors and will allow easy approach to T cell commitment studies.
CITATION STYLE
Lancrin, C., Schneider, E., Lambolez, F., Arcangeli, M. L., Garcia-Cordier, C., Rocha, B., & Ezine, S. (2002). Major T cell progenitor activity in bone marrow-derived spleen colonies. Journal of Experimental Medicine, 195(7), 919–929. https://doi.org/10.1084/jem.20011475
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