Unravelling human hematopoietic progenitor cell diversity through association with intrinsic regulatory factors.

ATAC-seq bone marrow cord blood erythrocyte/megakaryocyte lineage fetal liver hematopoietic stem and progenitor cell human hematopoiesis mass cytometry mobilized peripheral blood molecular regulator myeloid lineage pseudotime single-cell trajectory analysis transcription factor

Journal

bioRxiv : the preprint server for biology
Titre abrégé: bioRxiv
Pays: United States
ID NLM: 101680187

Informations de publication

Date de publication:
30 Aug 2023
Historique:
pubmed: 11 9 2023
medline: 11 9 2023
entrez: 11 9 2023
Statut: epublish

Résumé

Hematopoietic stem and progenitor cell (HSPC) transplantation is an essential therapy for hematological conditions, but finer definitions of human HSPC subsets with associated function could enable better tuning of grafts and more routine, lower-risk application. To deeply phenotype HSPCs, following a screen of 328 antigens, we quantified 41 surface proteins and functional regulators on millions of CD34+ and CD34- cells, spanning four primary human hematopoietic tissues: bone marrow, mobilized peripheral blood, cord blood, and fetal liver. We propose more granular definitions of HSPC subsets and provide new, detailed differentiation trajectories of erythroid and myeloid lineages. These aspects of our revised human hematopoietic model were validated with corresponding epigenetic analysis and

Identifiants

pubmed: 37693547
doi: 10.1101/2023.08.30.555623
pmc: PMC10491219
pii:
doi:

Types de publication

Preprint

Langues

eng

Subventions

Organisme : NIA NIH HHS
ID : P30 AG066515
Pays : United States
Organisme : NIBIB NIH HHS
ID : DP2 EB024246
Pays : United States
Organisme : NCI NIH HHS
ID : U24 CA224309
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG056287
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG057915
Pays : United States
Organisme : NIA NIH HHS
ID : U19 AG065156
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG068279
Pays : United States
Organisme : NHLBI NIH HHS
ID : U54 HL165445
Pays : United States

Déclaration de conflit d'intérêts

Declaration of interests I.S. is an employee of bluebird bio. The remaining authors declare no competing interests.

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Auteurs

Patricia Favaro (P)

Department of Pathology, Stanford University.
These authors contributed equally.

David R Glass (DR)

Department of Pathology, Stanford University.
Immunology Graduate Program, Stanford University.
Present address: Vaccine and Infectious Diseases Division, Fred Hutchinson Cancer Center, Seattle, WA, USA.
These authors contributed equally.

Luciene Borges (L)

Department of Pathology, Stanford University.
Present address: Boehringer Ingelheim Pharmaceuticals, Inc., Ridgefield, CT, USA.
These authors contributed equally.

Reema Baskar (R)

Department of Pathology, Stanford University.
Present address: Genome Institute of Singapore.

Warren Reynolds (W)

Department of Pathology, Stanford University.

Daniel Ho (D)

Department of Pathology, Stanford University.

Trevor Bruce (T)

Department of Pathology, Stanford University.

Dmitry Tebaykin (D)

Department of Pathology, Stanford University.

Vanessa M Scanlon (VM)

Department of Laboratory Medicine, Yale School of Medicine.
Present address: Center for Regenerative Medicine and Skeletal Biology, University of Connecticut Health.

Ilya Shestopalov (I)

bluebird bio, inc.

Sean C Bendall (SC)

Department of Pathology, Stanford University.
Immunology Graduate Program, Stanford University.
Lead author.

Classifications MeSH