Evidence map›Paper›PMID 36788616›Full record

ArticleCell communication and signaling : CCS2023

Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin.

Ilker A Deniz, Jana Karbanová, Manja Wobus, Martin Bornhäuser, Pauline Wimberger, Jan Dominik Kuhlmann, Denis Corbeil

Open access · goldAbstract readVideo-Audio Media
In one paragraph

Article in Cell communication and signaling : CCS, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
24.7field-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

46 citing papers in PubMed, 86 citations in OpenAlex.

  1. Article
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  9. Review
  10. Migrasomes: A Novel Target for Cancer Treatment.Current cancer drug targets · 2026
    Review
  11. Article
  12. Article
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  18. Deciphering the Regulatory Networks of the Migrasome-Associated Cell Subpopulation in Heterotopic Ossification via Multi-Omics Analysis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  19. Review
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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

7 authors at 4 institutions in 1 country.

Ilker A DenizBiotechnology Center (BIOTEC) and Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, 01307, Dresden, Germany.
Jana KarbanováBiotechnology Center (BIOTEC) and Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, 01307, Dresden, Germany.
Manja WobusDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, Technische Universität Dresden, 01307, Dresden, Germany.
Martin BornhäuserDepartment of Internal Medicine I, University Hospital Carl Gustav Carus, Technische Universität Dresden, 01307, Dresden, Germany.
Pauline WimbergerNational Center for Tumor Diseases (NCT) & German Cancer Research Center (DKFZ) & Faculty of Medicine, University Hospital Carl Gustav Carus & Technische Universität Dresden & Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Dresden and Heidelberg, Germany.
Jan Dominik KuhlmannNational Center for Tumor Diseases (NCT) & German Cancer Research Center (DKFZ) & Faculty of Medicine, University Hospital Carl Gustav Carus & Technische Universität Dresden & Helmholtz-Zentrum Dresden-Rossendorf (HZDR), Dresden and Heidelberg, Germany.
Denis CorbeilBiotechnology Center (BIOTEC) and Center for Molecular and Cellular Bioengineering, Technische Universität Dresden, 01307, Dresden, Germany. denis.corbeil@tu-dresden.de.
TU Dresden · DEHelmholtz-Zentrum Dresden-Rossendorf · DENational Center for Tumor Diseases · DEUniversity Hospital Heidelberg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMultipotent mesenchymal stromal cells (MSCs) are precursors of various cell types. Through soluble factors, direct cell-cell interactions and other intercellular communication mechanisms such as extracellular vesicles and tunneling nanotubes, MSCs support tissue homeostasis. In the bone marrow microenvironment, they promote hematopoiesis. The interaction between MSCs and cancer cells enhances the cancer and metastatic potential. Here, we have demonstrated that plastic-adherent MSCs isolated from human bone marrow generate migrasomes, a newly discovered organelle playing a role in intercellular communication.

resultsMigrasomes are forming a network with retraction fibers behind the migrating MSCs or surrounding them after membrane retraction. The MSC markers, CD44, CD73, CD90, CD105 and CD166 are present on the migrasome network, the latter being specific to migrasomes. Some migrasomes harbor the late endosomal GTPase Rab7 and exosomal marker CD63 indicating the presence of multivesicular bodies. Stromal cell-derived factor 1 (SDF-1) was detected in migrasomes, suggesting that they play a chemoattractant role. Co-cultures with KG-1a leukemic cells or primary CD34

conclusionOverall, we described a novel mechanism used by MSCs to communicate with cells of hematopoietic origin and further studies are needed to decipher all biological aspects of migrasomes in the healthy and transformed bone marrow microenvironment. Video Abstract.

Indexed as

Chemotactic FactorsMesenchymal Stem CellsAntigens, CD34Bone Marrow CellsCell DifferentiationCell Membrane StructuresCells, CulturedHematopoietic Stem CellsHumansNanotubesStromal CellsAntigens, CD34Chemotactic FactorsTunneling NanotubesCellular adhesionExtracellular vesicleHematopoietic stem cellIntercellular signalingMesenchymal stromal cellMigrasomeMotility

Identifiers

PMID36788616
PMCPMC9926842
OpenAlexW4320726013

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.