Evidence map›Paper›PMID 23850217›Full record

ReviewDifferentiation; research in biological diversity2013

Biomechanical force in blood development: extrinsic physical cues drive pro-hematopoietic signaling.

Hyun Jung Lee, Nan Li, Siobahn M Evans, Miguel F Diaz, Pamela L Wenzel

Open access · greenAbstract readReview
In one paragraph

Review in Differentiation; research in biological diversity, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

31 citing papers in PubMed, 54 citations in OpenAlex.

  1. Blood Flow Regulates Metabolism in Hematopoietic Development.Advances in experimental medicine and biology · 2026
    Review
  2. Review
  3. Review
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  5. Pumping up the blood progenitors by Piezo.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Biomechanical cues as master regulators of hematopoietic stem cell fate.Cellular and molecular life sciences : CMLS · 2021
    Review
  11. Article
  12. Article
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  16. 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

5 authors at 2 institutions in 1 country.

Hyun Jung LeeChildren's Regenerative Medicine Program, Department of Pediatric Surgery, University of Texas Medical School at Houston, Houston, TX 77030, USA; Center for Stem Cell and Regenerative Medicine, The Brown Foundation Institute of Molecular Medicine, University of Texas Health Science Center at Houston, Houston, TX 77030, USA.
Nan Li
Siobahn M Evans
Miguel F Diaz
Pamela L Wenzel
The University of Texas Health Science Center at Houston · USBrown Foundation · US

Funding

Identification of biomechanical pathways that promote hematopoiesisK01DK092365 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WENZEL, PAMELA LYNN · 2011 to 2015
$708k
NIDDK NIH HHS 1K01DK092365NIDDK NIH HHS K01 DK092365
6 · The paper itself

Abstract

The hematopoietic system is dynamic during development and in adulthood, undergoing countless spatial and temporal transitions during the course of one's life. Microenvironmental cues in the many unique hematopoietic niches differ, characterized by distinct soluble molecules, membrane-bound factors, and biophysical features that meet the changing needs of the blood system. Research from the last decade has revealed the importance of substrate elasticity and biomechanical force in determination of stem cell fate. Our understanding of the role of these factors in hematopoiesis is still relatively poor; however, the developmental origin of blood cells from the endothelium provides a model for comparison. Many endothelial mechanical sensors and second messenger systems may also determine hematopoietic stem cell fate, self renewal, and homing behaviors. Further, the intimate contact of hematopoietic cells with mechanosensitive cell types, including osteoblasts, endothelial cells, mesenchymal stem cells, and pericytes, places them in close proximity to paracrine signaling downstream of mechanical signals. The objective of this review is to present an overview of the sensors and intracellular signaling pathways activated by mechanical cues and highlight the role of mechanotransductive pathways in hematopoiesis.

Indexed as

HematopoiesisMechanotransduction, CellularAnimalsHematopoietic Stem CellsHumansStem Cell NicheStress, MechanicalADAMa disintegrin and metalloproteaseAGMaorta-gonad-mesonephrosBiomechanical forcecalcium sensing receptorCaSRCellular microenvironmentchemokine C-X-C motif receptorCXCRDAGdelta-likediacylglycerolDllECMextracellular matrixFAFAKfetal liver kinase-1Flk-1focal adhesionfocal adhesion kinaseFrizzledFZDGPCRG protein-coupled receptorhematopoietic stem and progenitor cellshematopoietic stem cellHematopoietic stem cellsHemogenic endotheliumHSCHSPChuman umbilical vein endothelial cellsHUVECILKinositol triphosphateintegrin linked kinaseIP3MAPKMechanotransductionmitogen activated protein kinaseNICDnitric oxide synthaseNOSNotch intracellular domainPGE2phosphatidylinositide 3-kinasephospholipase CPI3KPKAPKDPLCpolycystinprostaglandin E2protein kinase ARho-associated protein kinaseROCKS1PS1PR/EDG1SDF1Shear stresssphingosine 1-phosphatesphingosine 1-phosphate receptorstromal derived factor 1transient receptor potential vallinoid type 4TRPV4

Identifiers

PMID23850217
PMCPMC3795909
OpenAlexW2054227456

What OpenQuestion holds

Textmetadata
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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.