| Literature DB >> 17785806 |
Kyoko Masuda1, Kiyokazu Kakugawa, Toshinori Nakayama, Nagahiro Minato, Yoshimoto Katsura, Hiroshi Kawamoto.
Abstract
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.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17785806 DOI: 10.4049/jimmunol.179.6.3699
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422