Abstract

Common lymphoid progenitors (CLPs) are thought to represent major intermediates in the transition of hematopoietic stem cells (HSCs) to B lineage lymphocytes. However, it has been obvious for some time that CLPs are heterogeneous, and there has been controversy concerning their differentiation potential. We have now resolved four Flt3+ CLP subsets that are relatively homogenous and capable of forming B cells. Differentiation potential and gene expression patterns suggest Flt3+ CLPs lacking both Ly6D and RAG-1 are the least differentiated. In addition to B cells, they generate natural killer (NK) and dendritic cells (DCs). At the other extreme is a subset of the recently described Flt3+ Ly6D+ CLPs that have a history of RAG-1 expression and are B lineage restricted. These relatively abundant and potent CLPs were depleted within 48 hours of acute in vivo estrogen elevation, suggesting they descend from hormone regulated progenitors. This contrasts with the hormone insensitivity of other CLP subsets that include NK lineage progenitors. This progenitor heterogeneity and differentiation complexity may add flexibility in response to environmental changes. Expression of RAG-1 and display of Ly6D are both milestone events, but they are neither synchronized nor dependent on each other.

Highlights

  • Relationships between hematopoietic stem cells (HSCs) and B lineage lymphocytes have long been studied as a model for differentiation and as one that is informative about several diseases

  • Flt3 is up-regulated as HSCs give rise to very primitive lymphoid primed multipotent progenitors (LMPPs)/early lymphoid progenitors (ELPs) [5,12,16]

  • We found that both RAG-1/tdRFP positive and negative categories of Common lymphoid progenitors (CLPs) include Flt3+ cells

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Summary

Introduction

Relationships between hematopoietic stem cells (HSCs) and B lineage lymphocytes have long been studied as a model for differentiation and as one that is informative about several diseases. Display of Flt, a history of RAG-1 locus activation and expression of Ly6D are all well-established differentiation milestones in the B lymphocyte lineage [7,12,13,14,15]. Models based on those parameters have allowed subdivision of lymphoid progenitors, and helped to position B lineage progenitors in a sequence [5,8,9]. It has been unclear if there is a single, strict order to these events

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