Hartman Institute for Therapeutic Organ Regeneration

Multipotent progenitors and hematopoietic stem cells arise independently from hemogenic endothelium in the mouse embryo.

TitleMultipotent progenitors and hematopoietic stem cells arise independently from hemogenic endothelium in the mouse embryo.
Publication TypeJournal Article
Year of Publication2021
AuthorsDignum T, Varnum-Finney B, Srivatsan SR, Dozono S, Waltner O, Heck AM, Ishida T, Nourigat-McKay C, Jackson DL, Rafii S, Trapnell C, Bernstein ID, Hadland B
JournalCell Rep
Volume36
Issue11
Pagination109675
Date Published2021 Sep 14
ISSN2211-1247
KeywordsAnimals, Cell Differentiation, Cell Lineage, Cell Self Renewal, Coculture Techniques, Embryo, Mammalian, Female, Hemangioblasts, Hematopoiesis, Hematopoietic Stem Cells, Male, Mice, Mice, Inbred C57BL, Multipotent Stem Cells, Receptors, CXCR4, Transcription, Genetic
Abstract

<p>During embryogenesis, waves of hematopoietic progenitors develop from hemogenic endothelium (HE) prior to the emergence of self-renewing hematopoietic stem cells (HSCs). Although previous studies have shown that yolk-sac-derived erythromyeloid progenitors and HSCs emerge from distinct populations of HE, it remains unknown whether the earliest lymphoid-competent progenitors, multipotent progenitors, and HSCs originate from common HE. In this study, we demonstrate by clonal assays and single-cell transcriptomics that rare HE with functional HSC potential in the early murine embryo are distinct from more abundant HE with multilineage hematopoietic potential that fail to generate HSCs. Specifically, HSC-competent HE are characterized by expression of CXCR4 surface marker and by higher expression of genes tied to arterial programs regulating HSC dormancy and self-renewal. Taken together, these findings suggest a revised model of developmental hematopoiesis in which the initial populations of multipotent progenitors and HSCs arise independently from HE with distinct phenotypic and transcriptional properties.</p>

DOI10.1016/j.celrep.2021.109675
Alternate JournalCell Rep
PubMed ID34525376
PubMed Central IDPMC8478150
Grant ListK08 HL140143 / HL / NHLBI NIH HHS / United States
P30 CA015704 / CA / NCI NIH HHS / United States
R35 HL150809 / HL / NHLBI NIH HHS / United States
RC2 DK114777 / DK / NIDDK NIH HHS / United States

Weill Cornell Medicine
Hartman Institute for Therapeutic Organ Regeneration
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