Evidence map›Paper›PMID 33878141›Full record

ArticlePloS one2021

Human hematopoietic microenvironments.

Helene Bjoerg Kristensen, Thomas Levin Andersen, Andrea Patriarca, Klaus Kallenbach, Birgit MacDonald, Tanja Sikjaer, Charlotte Ejersted, Jean-Marie Delaisse

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Artificial Intelligence in Bone Marrow Histological Diagnostics: Potential Applications and Challenges.Pathobiology : journal of immunopathology, molecular and cellular biology · 2024
    Review
  4. Review
  5. Closer to Nature: The Role of MSCs in Recreating the Microenvironment of the Hematopoietic Stem Cell Niche in vitro.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2022
    Review
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

8 authors at 4 institutions in 1 country.

Helene Bjoerg KristensenDepartment of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.ORCID 0000-0002-3695-3650
Thomas Levin AndersenDepartment of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.
Andrea PatriarcaDivision of Hematology, Department of Oncology, Hospital "Maggiore della Carità", Novara, Italy.ORCID 0000-0003-4415-2906
Klaus KallenbachDepartment of Pathology, Zealand University Hospital, Roskilde, Denmark.
Birgit MacDonaldDepartment of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.
Tanja SikjaerDepartment of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.
Charlotte EjerstedDepartment of Endocrinology, Odense University Hospital, Odense, Denmark.
Jean-Marie DelaisseDepartment of Clinical Cell Biology, Institute of Regional Health Science, University of Southern Denmark, Lillebaelt Hospital, Vejle, Denmark.
University of Southern Denmark · DKAarhus University Hospital · DKOdense University Hospital · DKZealand University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dormancy of hematopoietic stem cells and formation of progenitors are directed by signals that come from the bone marrow microenvironment. Considerable knowledge has been gained on the murine hematopoietic stem cell microenvironment, while less so on the murine progenitor microenvironment and even less so on these microenvironments in humans. Characterization of these microenvironments is decisive for understanding hematopoiesis and finding new treatment modalities against bone marrow malignancies in the clinic. However, it is equally challenging, because hematopoietic stem cells are difficult to detect in the complex bone marrow landscape. In the present study we are characterizing the human hematopoietic stem cell and progenitor microenvironment. We obtained three adjacent bone marrow sections from ten healthy volunteers. One was used to identify a population of CD34+/CD38- "hematopoietic stem cells and multipotent progenitors" and a population of CD34+/CD38+ "progenitors" based on immunofluorescence pattern/intensity and cellular morphology. The other two were immunostained respectively for CD34/CD56 and for CD34/SMA. Using the combined information we performed a non-computer-assisted quantification of nine bone marrow components (adipocytes, megakaryocytes, bone surfaces, four different vessel types (arteries, capillaries, sinusoids and collecting sinuses), other "hematopoietic stem cells and multipotent progenitors" and other "progenitors") within 30 μm of "hematopoietic stem cells and multipotent progenitors", "progenitors", and "random cell profiles". We show that the microenvironment of the "hematopoietic stem cells and multipotent progenitors" is significantly enriched in sinusoids and megakaryocytes, while the microenvironment of the "progenitors" is significantly enriched in capillaries, other "progenitors", bone surfaces and arteries.

Indexed as

AdipocytesAdultAgedAntigens, CD34Bone MarrowBone Marrow CellsCell DifferentiationCells, CulturedCell SeparationFemaleFlow CytometryHematopoiesisHematopoietic Stem CellsHematopoietic Stem Cell TransplantationHumansImmunophenotypingAntigens, CD34Membrane Glycoproteins

Identifiers

PMID33878141
PMCPMC8057613
OpenAlexW3154243080

What OpenQuestion holds

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LicenceCC BY
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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 OpenQuestion graph.