Abstract
Common lymphoid progenitors (CLPs) clonally produce both B- and T-cell lineages, but have little myeloid potential in vivo. However, some studies claim that the upstream lymphoid-primed multipotent progenitor (LMPP) is the thymic seeding population, and suggest that CLPs are primarily B-cell-restricted. To identify surface proteins that distinguish functional CLPs from B-cell progenitors, we used a new computational method of Mining Developmentally Regulated Genes (MiDReG). We identified Ly6d, which divides CLPs into two distinct populations: one that retains full in vivo lymphoid potential and produces more thymocytes at early timepoints than LMPP, and another that behaves essentially as a B-cell progenitor.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 2376-2381 |
| Number of pages | 6 |
| Journal | Genes and Development |
| Volume | 23 |
| Issue number | 20 |
| DOIs | |
| State | Published - Oct 15 2009 |
| Externally published | Yes |
Keywords
- B-cell development
- Fate decisions
- Hematopoiesis
- Lymphopoiesis
- T-cell development
ASJC Scopus subject areas
- General Medicine
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