Evidence map›Paper›PMID 34021930›Full record

ArticleAmerican journal of hematology2021

Comprehensive phenotyping of erythropoiesis in human bone marrow: Evaluation of normal and ineffective erythropoiesis.

Hongxia Yan, Abdullah Ali, Lionel Blanc, Anupama Narla, Joseph M Lane, Erjing Gao, Julien Papoin, John Hale, Christopher D Hillyer, Naomi Taylor and 4 more

Open access · bronzeAbstract read
In one paragraph

Article in American journal of hematology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.3field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

33 citing papers in PubMed, 46 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors at 7 institutions in 3 countries.

Hongxia YanNew York Blood Center, New York, New York, USA.ORCID 0000-0002-8187-2788
Abdullah AliMyelodysplastic Syndromes Center, Columbia University, New York, New York, USA.
Lionel BlancThe Feinstein Institute for Medical Research, Manhasset, New York, USA.
Anupama NarlaStanford University School of Medicine, Stanford, California, USA.ORCID 0000-0003-2325-3388
Joseph M LaneDepartment of Orthopaedic Surgery, Hospital for Special Surgery, New York, New York, USA.
Erjing GaoNew York Blood Center, New York, New York, USA.
Julien PapoinThe Feinstein Institute for Medical Research, Manhasset, New York, USA.
John HaleNew York Blood Center, New York, New York, USA.
Christopher D HillyerNew York Blood Center, New York, New York, USA.
Naomi TaylorInstitut de Génétique Moléculaire de Montpellier, University of Montpellier, CNRS, Montpellier, France.
Patrick G GallagherDepartment of Pediatrics, Yale University School of Medicine, New Haven, Connecticut, USA.
Azra RazaMyelodysplastic Syndromes Center, Columbia University, New York, New York, USA.
Sandrina KinetInstitut de Génétique Moléculaire de Montpellier, University of Montpellier, CNRS, Montpellier, France.
Narla MohandasNew York Blood Center, New York, New York, USA.
New York Blood Center · USCentre National de la Recherche Scientifique · FRFeinstein Institute for Medical Research · USItalian Foundation of Myelodysplastic Syndromes · ITHospital for Special Surgery · USStanford University · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
YEAST MEMBRANE CYTOSKELETONP01DK032094 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI NARLA, MOHANDAS · 1987 to 2021
$26.7M
Reprogramming hematopoietic stem cell (HSC) differentiation via metabolic conditZIABC011924 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TAYLOR, NAOMI · 2019 to 2025
$9.0M
Molecular targeting of erythroid progenitor cells in normal and disordered human erythropoiesisR01HL144436 · NHLBI · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI BLANC, LIONEL · 2019 to 2023
$2.5M
The Role of Erythroblastic Islands in Anemia of InflammationR01HL152099 · NHLBI · CINCINNATI CHILDRENS HOSP MED CTR · PI BLANC, LIONEL, KALFA, THEODOSIA ANASTASIOS · 2020 to 2023
$2.5M
NCATS NIH HHS UL1 TR001863NHLBI NIH HHS R01 HL144436NHLBI NIH HHS R01 HL152099NIDDK NIH HHS P01 DK032094
6 · The paper itself

Abstract

Identification of stage-specific erythroid cells is critical for studies of normal and disordered human erythropoiesis. While immunophenotypic strategies have previously been developed to identify cells at each stage of terminal erythroid differentiation, erythroid progenitors are currently defined very broadly. Refined strategies to identify and characterize BFU-E and CFU-E subsets are critically needed. To address this unmet need, a flow cytometry-based technique was developed that combines the established surface markers CD34 and CD36 with CD117, CD71, and CD105. This combination allowed for the separation of erythroid progenitor cells into four discrete populations along a continuum of progressive maturation, with increasing cell size and decreasing nuclear/cytoplasmic ratio, proliferative capacity and stem cell factor responsiveness. This strategy was validated in uncultured, primary erythroid cells isolated from bone marrow of healthy individuals. Functional colony assays of these progenitor populations revealed enrichment of BFU-E only in the earliest population, transitioning to cells yielding BFU-E and CFU-E, then CFU-E only. Utilizing CD34/CD105 and GPA/CD105 profiles, all four progenitor stages and all five stages of terminal erythroid differentiation could be identified. Applying this immunophenotyping strategy to primary bone marrow cells from patients with myelodysplastic syndrome, identified defects in erythroid progenitors and in terminal erythroid differentiation. This novel immunophenotyping technique will be a valuable tool for studies of normal and perturbed human erythropoiesis. It will allow for the discovery of stage-specific molecular and functional insights into normal erythropoiesis as well as for identification and characterization of stage-specific defects in inherited and acquired disorders of erythropoiesis.

Indexed as

ErythropoiesisAntigens, CDAntigens, CD34Bone Marrow CellsCells, CulturedEndoglinErythroid CellsErythroid Precursor CellsFlow CytometryHumansImmunophenotypingAntigens, CDAntigens, CD34Endoglin

Identifiers

PMID34021930
PMCPMC8355124
OpenAlexW3161594315

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.