Imaging flow cytometry reveals that granulocyte colony-stimulating factor treatment causes loss of erythroblastic islands in the mouse bone marrow.


Journal

Experimental hematology
ISSN: 1873-2399
Titre abrégé: Exp Hematol
Pays: Netherlands
ID NLM: 0402313

Informations de publication

Date de publication:
02 2020
Historique:
received: 11 12 2019
revised: 03 02 2020
accepted: 04 02 2020
pubmed: 12 2 2020
medline: 15 7 2020
entrez: 12 2 2020
Statut: ppublish

Résumé

The erythroblastic island (EBI) is a multicellular structure forming an erythropoietic niche consisting of a central macrophage surrounded by a rosette of maturing erythroblasts. Since their discovery more than 60 years ago, simultaneous quantification and visualization of EBIs remain difficult. Although flow cytometry enables high-throughput quantification of cell aggregates co-expressing macrophage and erythroblast markers, it cannot visually confirm whether the aggregates are genuine EBIs. While immunofluorescence microscopy allows visualization of EBIs, its low throughput limits its use for quantification. In the current study we employed nine-channel imaging flow cytometry (IFC) to develop a method to directly visualize and quantify EBIs in the mouse bone marrow. We found that EBI central macrophages do express F4/80, VCAM-1, and CD169, but not CD11b or Ly6G, and that CD11b

Identifiants

pubmed: 32045657
pii: S0301-472X(20)30042-4
doi: 10.1016/j.exphem.2020.02.003
pii:
doi:

Substances chimiques

Antigens, Differentiation 0
Granulocyte Colony-Stimulating Factor 143011-72-7

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

33-42

Informations de copyright

Copyright © 2020 ISEH -- Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest disclosure The authors declare no competing financial interests.

Auteurs

Joshua Tay (J)

Stem Cell and Cancer Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia.

Kavita Bisht (K)

Stem Cell Biology Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia.

Crystal McGirr (C)

Stem Cell Biology Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia.

Susan M Millard (SM)

Bones and Immunology Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia.

Allison R Pettit (AR)

Bones and Immunology Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia.

Ingrid G Winkler (IG)

Stem Cell and Cancer Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia. Electronic address: ingrid.winkler@mater.uq.edu.au.

Jean-Pierre Levesque (JP)

Stem Cell Biology Group, Mater Research-University of Queensland Translational Research Institute, Woolloongabba, QLD, Australia. Electronic address: jp.levesque@mater.uq.edu.au.

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Classifications MeSH