Single-cell RNA sequencing reveals developmental heterogeneity among early lymphoid progenitors

Abstract

Single-cell RNA sequencing is a powerful technology for assessing heterogeneity within defined cell populations. Here, we describe the heterogeneity of a B220⁺CD117^intCD19^-NK1.1^- uncommitted hematopoietic progenitor having combined lymphoid and myeloid potential. Phenotypic and functional assays revealed four subpopulations within the progenitor with distinct lineage developmental potentials. Among them, the Ly6D⁺SiglecH^-CD11c^- fraction was lymphoid-restricted exhibiting strong B-cell potential, whereas the Ly6D^-SiglecH^-CD11c^- fraction showed mixed lympho-myeloid potential. Single-cell RNA sequencing of these subsets revealed that the latter population comprised a mixture of cells with distinct lymphoid and myeloid transcriptional signatures and identified a subgroup as the potential precursor of Ly6D⁺SiglecH^-CD11c^- Subsequent functional assays confirmed that B220⁺CD117^intCD19^-NK1.1^- single cells are, with rare exceptions, not bipotent for lymphoid and myeloid lineages. A B-cell priming gradient was observed within the Ly6D⁺SiglecH^-CD11c^- subset and we propose a herein newly identified subgroup as the direct precursor of the first B-cell committed stage. Therefore, the apparent multipotency of B220⁺CD117^intCD19^-NK1.1^- progenitors results from underlying heterogeneity at the single-cell level and highlights the validity of single-cell transcriptomics for resolving cellular heterogeneity and developmental relationships among hematopoietic progenitors.

Keywords: hematopoiesis; heterogeneity; lineage priming; multipotentiality; single‐cell RNA sequencing.