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Distinct myeloid progenitor-differentiation pathways identified through single-cell RNA sequencing.

TitleDistinct myeloid progenitor-differentiation pathways identified through single-cell RNA sequencing.
Publication TypeJournal Article
Year of Publication2016
AuthorsDrissen R, Buza-Vidas N, Woll P, Thongjuea S, Gambardella A, Giustacchini A, Mancini E, Zriwil A, Lutteropp M, Grover A, Mead A, Sitnicka E, Jacobsen SEirik W, Nerlov C
JournalNat Immunol
Volume17
Issue6
Pagination666-676
Date Published2016 06
ISSN1529-2916
KeywordsAnimals, Antigens, CD, Cell Differentiation, Cell Lineage, Cells, Cultured, Computational Biology, fms-Like Tyrosine Kinase 3, GATA1 Transcription Factor, Hematopoiesis, Immunity, Innate, Lymphocytes, Mice, Mice, Inbred C57BL, Mice, Knockout, Mice, Transgenic, Myeloid Cells, Myeloid Progenitor Cells, Sequence Analysis, RNA, Single-Cell Analysis, Tissue Array Analysis
Abstract

According to current models of hematopoiesis, lymphoid-primed multi-potent progenitors (LMPPs) (Lin(-)Sca-1(+)c-Kit(+)CD34(+)Flt3(hi)) and common myeloid progenitors (CMPs) (Lin(-)Sca-1(+)c-Kit(+)CD34(+)CD41(hi)) establish an early branch point for separate lineage-commitment pathways from hematopoietic stem cells, with the notable exception that both pathways are proposed to generate all myeloid innate immune cell types through the same myeloid-restricted pre-granulocyte-macrophage progenitor (pre-GM) (Lin(-)Sca-1(-)c-Kit(+)CD41(-)FcγRII/III(-)CD150(-)CD105(-)). By single-cell transcriptome profiling of pre-GMs, we identified distinct myeloid differentiation pathways: a pathway expressing the gene encoding the transcription factor GATA-1 generated mast cells, eosinophils, megakaryocytes and erythroid cells, and a pathway lacking expression of that gene generated monocytes, neutrophils and lymphocytes. These results identify an early hematopoietic-lineage bifurcation that separates the myeloid lineages before their segregation from other hematopoietic-lineage potential.

DOI10.1038/ni.3412
Alternate JournalNat. Immunol.
PubMed ID27043410
PubMed Central IDPMC4972405
Grant ListMR/M00919X/1 / / Medical Research Council / United Kingdom
087371 / / Wellcome Trust / United Kingdom
G0902418 / / Medical Research Council / United Kingdom
G0701761 / / Medical Research Council / United Kingdom
MR/L006340/1 / / Medical Research Council / United Kingdom
11-0724 / / Worldwide Cancer Research / United Kingdom
G0801073 / / Medical Research Council / United Kingdom
MC_UU_12009/5 / / Medical Research Council / United Kingdom
G0501838 / / Medical Research Council / United Kingdom
MC_UU_12009/7 / / Medical Research Council / United Kingdom
MR/L012766/1 / / Medical Research Council / United Kingdom
G0900892 / / Medical Research Council / United Kingdom
MC_UU_12025 / / Medical Research Council / United Kingdom
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