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Cloning thymic precursor cells: Demonstration that individual pro-T1 cells have dual T-NK potential and individual pro-T2 cells have dual alpha beta-gamma delta T cell potential

  1. Author:
    Lee, C. K.
    Kim, K.
    Geiman, T. M.
    Murphy, W. J.
    Muegge, K.
    Durum, S. K.
  2. Author Address

    Lee CK NCI, Immunoregulat Lab, Div Basic Sci Frederick, MD 21702 USA NCI, Immunoregulat Lab, Div Basic Sci Frederick, MD 21702 USA NCI, SAIC Frederick, MD 21702 USA
    1. Year: 1999
  1. Journal: Cellular Immunology
    1. 191
    2. 2
    3. Pages: 139-144
  2. Type of Article: Article
  1. Abstract:

    Thymic progenitors have the capacity to generate alpha beta T cells, gamma delta T cells, and NK cells. To determine whether these three lineages derive from a single precursor cell or from different precursors, a procedure was developed for cloning precursor cells from mouse embryonic thymus. The progeny of each pro-T cell clone were then tested for the potential to generate alpha beta, gamma delta, and NK cells. Of these precursor clones, about half displayed dual potential, developing into either T cells or NK cells, demonstrating the existence of a common T/NK precursor cell in the thymus. The other half of the clones were restricted to T cell development. No precursor clones were restricted to NK development. The common T/NK precursors were shown to be of the pro-T1 (CD25(-)) stage whereas the T-restricted precursors were shown to be of the later pro-TS (CD25(+)) stage. Both alpha beta and gamma delta T cells were generated from all clones derived from either pro-T1 or -T2 precursors. This shows that commitment of a cell to the (YP versus gamma delta lineages does not precede rearrangement of the TCR genes (which occurs immediately after the pro-T2 stage). (C) 1999 Academic Press. [References: 28]

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