Evidence map›Paper›PMID 24268694›Full record

ArticleCell stem cell2014

Contractile forces sustain and polarize hematopoiesis from stem and progenitor cells.

Jae-Won Shin, Amnon Buxboim, Kyle R Spinler, Joe Swift, David A Christian, Christopher A Hunter, Catherine Léon, Christian Gachet, P C Dave P Dingal, Irena L Ivanovska and 3 more

Abstract read
In one paragraph

Article in Cell stem cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

77 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Mechanical confinement prevents ectopic platelet release.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  12. Article
  13. Review
  14. Review
  15. Article
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  17. Article
  18. Article
  19. Article
  20. Hematopoietic responses to SARS-CoV-2 infection.Cellular and molecular life sciences : CMLS · 2022
    Review

17 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Jae-Won ShinBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology and Pharmacology Graduate Groups, University of Pennsylvania, Philadelphia, PA 19104, USA.
Amnon BuxboimBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.
Kyle R SpinlerBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.
Joe SwiftBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.
David A ChristianDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Christopher A HunterDepartment of Pathobiology, School of Veterinary Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Catherine LéonUMR S949, Inserm, Université de Strasbourg, Établissement Français du Sang, Strasbourg, 67000, France.
Christian GachetUMR S949, Inserm, Université de Strasbourg, Établissement Français du Sang, Strasbourg, 67000, France.
P C Dave P DingalBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.
Irena L IvanovskaBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.
Florian RehfeldtBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA.
Joel Anne ChasisLife Sciences Division, University of California, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA; Division of Hematology/Oncology, University of California, San Francisco, San Francisco, CA 94143, USA.
Dennis E DischerBiophysical Engineering Lab, University of Pennsylvania, Philadelphia, PA 19104, USA; Cell and Molecular Biology and Pharmacology Graduate Groups, University of Pennsylvania, Philadelphia, PA 19104, USA. Electronic address: discher@seas.upenn.edu.

Funding

Institutional Clinical and Translational Science AwardUL1TR000003 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI FITZGERALD, GARRET A · 2012 to 2015
$38.9M
YEAST MEMBRANE CYTOSKELETONP01DK032094 · NIDDK · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI NARLA, MOHANDAS · 1987 to 2021
$26.7M
Research BaseP30DK090969 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI CARROLL, MARTIN · 2010 to 2015
$5.7M
SPECTRIN EXTENSIBILITY and CD47 CONNECTIONS &FUNCTIONR01HL062352 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 1999 to 2012
$3.3M
Nanoscience of 'Self' - reductionist approaches to hCD47 inhibition of phagocytesR01HL124106 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2014 to 2022
$3.1M
Carrier Shape Matters: Filomicelles, Long-circulation, and the EPR effectR01EB007049 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2006 to 2014
$2.8M
Understanding HIV escape using atomic force microscopyR21AI087516 · NIAID · CHILDREN'S HOSP OF PHILADELPHIA · PI DISCHER, DENNIS E., FINKEL, TERRI H · 2010 to 2011
$474k
Myocytes sense substrate stiffness - New materialsR21EB004489 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2005 to 2006
$415k
AFM(T) + FLUORESCENCE MEASUREMENTS ON SINGLE MOLECULESS10RR022575 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2007 to 2007
$382k
Matrix-induced Myogenesis & Pharmaco-Screens of MSCsR21AR056128 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2008 to 2009
$364k
CD47-Display on NanomaterialsR21EB003164 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2003 to 2004
$360k
Worm-like Micelles for Targeted Delivery and ImagingR21EB004000 · NIBIB · UNIVERSITY OF PENNSYLVANIA · PI DISCHER, DENNIS E. · 2004 to 2005
$348k
NCATS NIH HHS 8UL1TR000003NCATS NIH HHS UL1 TR000003NCRR NIH HHS S10 RR022575NHLBI NIH HHS R01 HL062352NHLBI NIH HHS R01HL062352NHLBI NIH HHS R01 HL124106NIAID NIH HHS R21 AI087516NIAMS NIH HHS R21 AR056128NIBIB NIH HHS R01 EB007049NIBIB NIH HHS R01-EB007049NIBIB NIH HHS R21 EB003164NIBIB NIH HHS R21 EB004000NIBIB NIH HHS R21 EB004489NIDDK NIH HHS P01 DK032094NIDDK NIH HHS P01DK032094NIDDK NIH HHS P30-DK090969
6 · The paper itself

Abstract

Self-renewal and differentiation of stem cells depend on asymmetric division and polarized motility processes that in other cell types are modulated by nonmuscle myosin-II (MII) forces and matrix mechanics. Here, mass spectrometry-calibrated intracellular flow cytometry of human hematopoiesis reveals MIIB to be a major isoform that is strongly polarized in hematopoietic stem cells and progenitors (HSC/Ps) and thereby downregulated in differentiated cells via asymmetric division. MIIA is constitutive and activated by dephosphorylation during cytokine-triggered differentiation of cells grown on stiff, endosteum-like matrix, but not soft, marrow-like matrix. In vivo, MIIB is required for generation of blood, while MIIA is required for sustained HSC/P engraftment. Reversible inhibition of both isoforms in culture with blebbistatin enriches for long-term hematopoietic multilineage reconstituting cells by 5-fold or more as assessed in vivo. Megakaryocytes also become more polyploid, producing 4-fold more platelets. MII is thus a multifunctional node in polarized division and niche sensing.

Indexed as

Cell DifferentiationCell MovementApoptosisBlotting, WesternCell Culture TechniquesCell LineageCell ProliferationFlow CytometryHematopoiesisHematopoietic Stem CellsHeterocyclic Compounds, 4 or More RingsHumansMuscle ContractionNonmuscle Myosin Type IIANonmuscle Myosin Type IIBPhosphorylationblebbistatinHeterocyclic Compounds, 4 or More RingsNonmuscle Myosin Type IIANonmuscle Myosin Type IIB

Identifiers

PMID24268694
PMCPMC3969018

What OpenQuestion holds

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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.