Abstract
Using a human CD25 reporter transgene controlled by regulatory sequences from the gene encoding pre-T cell receptor α, we identified a common lymphocyte precursor (CLP-2) population that, in contrast to the previously identified CLP-1 population, was c-Kit-B220+. In short-term culture, the CLP-2 could be derived from the CLP-1 subset, and contained cells that in clonogenic assays were assessed to be bipotent precursors of T and B cells. Intravenous injection of bone marrow cells yielded a selective accumulation of CLP-2 thymic immigrants that in thymic organ culture generated mature αβ T cells. Although the CLP-2 subset may represent the most differentiated population with T cell potential before commitment to the B cell lineage, other subsets of thymic immigrants capable of generating T cells may exist.
Original language | English (US) |
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Pages (from-to) | 866-873 |
Number of pages | 8 |
Journal | Nature immunology |
Volume | 4 |
Issue number | 9 |
DOIs | |
State | Published - Sep 1 2003 |
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology