Evidence map›Paper›PMID 36876630›Full record

ArticleeLife2023

Identification of phenotypically, functionally, and anatomically distinct stromal niche populations in human bone marrow based on single-cell RNA sequencing.

Hongzhe Li, Sandro Bräunig, Parashar Dhapolar, Göran Karlsson, Stefan Lang, Stefan Scheding

Open access · goldAbstract read
In one paragraph

Article in eLife, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
11.0field-weighted citation impact, top 1% 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

34 citing papers in PubMed, 38 citations in OpenAlex.

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  12. Metabolomics of healthy hematopoietic stem cells and leukemic stem cells.Journal of clinical and translational research · 2025
    Article
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  19. Modeling of skeletal development and diseases using human pluripotent stem cells.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Review
  20. Matrix stiffness-dependent regulation of immunomodulatory genes in human MSCs is associated with the lncRNA CYTOR.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
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

6 authors at 1 institution in 1 country.

Hongzhe LiDivision of Molecular Hematology and Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0001-7788-878X
Sandro BräunigDivision of Molecular Hematology and Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0002-4418-0854
Parashar DhapolarDivision of Molecular Hematology and Stem Cell Center, Lund University, Lund, Sweden.
Göran KarlssonDivision of Molecular Hematology and Stem Cell Center, Lund University, Lund, Sweden.
Stefan LangDivision of Molecular Hematology and Stem Cell Center, Lund University, Lund, Sweden.
Stefan SchedingDivision of Molecular Hematology and Stem Cell Center, Lund University, Lund, Sweden.ORCID 0000-0002-8005-9568
Lund University · SE

Funding

Swedish Cancer Foundation 20-1163PjF 01HSwedish Childhood Cancer Foundation PR2018-0078Swedish Childhood Cancer Foundation PR2021-0065
6 · The paper itself

Abstract

Hematopoiesis is regulated by the bone marrow (BM) stroma. However, cellular identities and functions of the different BM stromal elements in humans remain poorly defined. Based on single-cell RNA sequencing (scRNAseq), we systematically characterized the human non-hematopoietic BM stromal compartment and we investigated stromal cell regulation principles based on the RNA velocity analysis using scVelo and studied the interactions between the human BM stromal cells and hematopoietic cells based on ligand-receptor (LR) expression using CellPhoneDB. scRNAseq led to the identification of six transcriptionally and functionally distinct stromal cell populations. Stromal cell differentiation hierarchy was recapitulated based on RNA velocity analysis and in vitro proliferation capacities and differentiation potentials. Potential key factors that might govern the transition from stem and progenitor cells to fate-committed cells were identified. In situ localization analysis demonstrated that different stromal cells were localized in different niches in the bone marrow. In silico cell-cell communication analysis further predicted that different stromal cell types might regulate hematopoiesis through distinct mechanisms. These findings provide the basis for a comprehensive understanding of the cellular complexity of the human BM microenvironment and the intricate stroma-hematopoiesis crosstalk mechanisms, thus refining our current view on human hematopoietic niche organization.

Indexed as

Bone MarrowHematopoietic Stem CellsBone Marrow CellsHematopoiesisHumansRNASequence Analysis, RNAStem Cell NicheRNAdifferentiation hierarchyhematopoietic microenvironmenthematopoietic-stromal communicationhumanhuman bone marrowregenerative medicinesingle-cell RNA sequencingstem cellsstromal stem/progenitor cells

Identifiers

PMID36876630
PMCPMC10097421
OpenAlexW4323294384

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.