T Cell Lineage Determination Precedes the Initiation of TCRβ Gene Rearrangement
Author(s) -
Kyoko Masuda,
Kiyokazu Kakugawa,
Toshinori Nakayama,
Nagahiro Minato,
Yoshimoto Katsura,
Hiroshi Kawamoto
Publication year - 2007
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.179.6.3699
Subject(s) - biology , lineage (genetic) , progenitor cell , t cell receptor , gene rearrangement , green fluorescent protein , microbiology and biotechnology , transgene , t cell , progenitor , gene , event (particle physics) , genetics , stem cell , immune system , physics , quantum mechanics
Loss of dendritic cell potential is one of the major events in intrathymic T cell development, during which the progenitors become determined to the T cell lineage. However, it remains unclear whether this event occurs in synchrony with another important event, TCRbeta chain gene rearrangement, which has been considered the definitive sign of irreversible T cell lineage commitment. To address this issue, we used transgenic mice in which GFP expression is controlled by the lck proximal promoter. We found that the double-negative (DN) 2 stage can be subdivided into GFP- and GFP+ populations, representing functionally different developmental stages in that the GFP-DN2, but not GFP+DN2, cells retain dendritic cell potential. The GFP+DN2 cells were found to undergo several rounds of proliferation before the initiation of TCRbeta rearrangement as evidenced by the diversity of D-Jbeta rearrangements seen in T cells derived from a single GFP+DN2 progenitor. These results indicated that the determination step of progenitors to the T cell lineage is a separable event from TCRbeta rearrangement.
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