Evidence map›Paper›PMID 32589864›Full record

ArticleCell stem cell2020

Intravital Imaging Reveals Motility of Adult Hematopoietic Stem Cells in the Bone Marrow Niche.

Samik Upadhaya, Oleg Krichevsky, Ilseyar Akhmetzyanova, Catherine M Sawai, David R Fooksman, Boris Reizis

Open access · bronzeAbstract read
In one paragraph

Article in Cell stem cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

42 citing papers in PubMed, 69 citations in OpenAlex.

  1. Article
  2. In vivo tracking of ex-vivo-generatedMolecular therapy : the journal of the American Society of Gene Therapy · 2025
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  3. Review
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  8. The evolving hematopoietic niche during development.Frontiers in molecular biosciences · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 3 countries.

Samik UpadhayaDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA.
Oleg KrichevskyPhysics Department, Ben Gurion University of the Negev, Beer-Sheva 84105, Israel.
Ilseyar AkhmetzyanovaDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Catherine M SawaiDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA; INSERM Unit 1218 ACTION Laboratory, University of Bordeaux, Bergonié Cancer Institute, 33076 Bordeaux, France.
David R FooksmanDepartment of Pathology, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: david.fooksman@einsteinmed.org.
Boris ReizisDepartment of Pathology, New York University Grossman School of Medicine, New York, NY 10016, USA. Electronic address: boris.reizis@nyulangone.org.
Albert Einstein College of Medicine · USNew York University · USBen-Gurion University of the Negev · ILInstitut Bergonié · FR

Funding

CD138 Regulates Competition of Antibody Secreting Cells for SurvivalR01HL141491 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI David R Fooksman · 2018 to 2026
$3.8M
Dissecting the aging of hematopoietic stem cells by genetic tracing in vivoR01AG049074 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI REIZIS, BORIS · 2015 to 2019
$1.7M
NHLBI NIH HHS R01 HL141491NIA NIH HHS R01 AG049074
6 · The paper itself

Abstract

Adult mammalian hematopoietic stem cells (HSCs) reside in the bone marrow (BM) but can be mobilized into blood for use in transplantation. HSCs interact with BM niche cells that produce growth factor c-Kit ligand (Kitl/SCF) and chemokine CXCL12, and were thought to be static and sessile. We used two-photon laser scanning microscopy to visualize genetically labeled HSCs in the BM of live mice for several hours. The majority of HSCs showed a dynamic non-spherical morphology and significant motility, undergoing slow processive motion interrupted by short stretches of confined motion. HSCs moved in the perivascular space and showed intermittent close contacts with SCF-expressing perivascular stromal cells. In contrast, mobilization-inducing blockade of CXCL12 receptor CXCR4 and integrins rapidly abrogated HSC motility and shape dynamics in real time. Our results reveal an unexpectedly dynamic nature of HSC residence in the BM and interaction with the SCF

Indexed as

Bone MarrowHematopoietic Stem CellsAnimalsBone Marrow CellsCell MovementChemokine CXCL12Intravital MicroscopyMiceStem Cell NicheChemokine CXCL12bone marrowCXCR4hematopoietic stem cellsintegrinsintravital microscopymobilizationmotilitystem cell nichestronal cells

Identifiers

PMID32589864
PMCPMC7415613
OpenAlexW3037229000

What OpenQuestion 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 OpenQuestion graph.