Coordinated regulation of self-renewal and cell cycle during human lympho-myeloid lineage restriction

Abstract

Abstract Recent studies indicate the human lympho-myeloid restriction process to be a different and more heterogeneous one than historically inferred. Here we describe the development of bulk and clonal culture systems that efficiently support early B-lymphoid differentiation and its use to elucidate the biological and molecular changes that accompany their initial restriction from subsets of CD34+ human cord blood cells with lympho-myeloid–limited potential. Analyses of these changes revealed that the acquisition of B-lymphoid– and neutrophil/monocyte (NM)–restricted properties are accompanied by a concomitantly accelerated and lineage-shared cell cycling activity and loss of self-renewal potential. Single-cell transcriptome analysis identified reduced expression of multiple self-renewal–associated genes and an accompanying heterogeneous activation of lineage-regulatory modules during the production of B, NM, and dendritic cell precursors. By applying a novel culture system that supports early human lymphoid differentiation, we uncovered a shared mechanism of proliferation control, along with persistent biological and transcriptional heterogeneity in cells undergoing B- and NM-lineage restriction.