Ly6d marks the earliest stage of B-cell specification and identifies the branchpoint between B-cell and T-cell development

Matthew A. Inlay, Deepta Bhattacharya, Debashis Sahoo, Thomas Serwold, Jun Seita, Holger Karsunky, Sylvia K. Plevritis, David L. Dill, Irving L. Weissman

Research output: Contribution to journalArticlepeer-review

231 Scopus citations

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 languageEnglish (US)
Pages (from-to)2376-2381
Number of pages6
JournalGenes and Development
Volume23
Issue number20
DOIs
StatePublished - Oct 15 2009
Externally publishedYes

Keywords

  • B-cell development
  • Fate decisions
  • Hematopoiesis
  • Lymphopoiesis
  • T-cell development

ASJC Scopus subject areas

  • General Medicine

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