Evidence map›Paper›PMID 18055451›Full record

ArticleStem cells (Dayton, Ohio)2008

Fluorophore-conjugated iron oxide nanoparticle labeling and analysis of engrafting human hematopoietic stem cells.

Dustin J Maxwell, Jesper Bonde, David A Hess, Sarah A Hohm, Ryan Lahey, Ping Zhou, Michael H Creer, David Piwnica-Worms, Jan A Nolta

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

24 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Transient loading of CD34International journal of nanomedicine · 2017
    Article
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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

9 authors at 5 institutions in 2 countries.

Dustin J MaxwellMolecular Imaging Center, Mallinckrodt Institute of Radiology, Department of Molecular Biology and Pharmacology, Washington University School of Medicine, St. Louis, Missouri, USA.
Jesper Bonde
David A Hess
Sarah A Hohm
Ryan Lahey
Ping Zhou
Michael H Creer
David Piwnica-Worms
Jan A Nolta
University of California, Davis · USMallinckrodt (United States) · USWashington University in St. Louis · USSaint Louis University · USWestern University · CA

Funding

WU-MDACC Inter-Institutional Molecular Imaging CenterP50CA094056 · NCI · WASHINGTON UNIVERSITY · PI KOPAN, RAPHAEL · 2002 to 2016
$26.3M
MEMBRANE PERMEANT PEPTIDES FOR IMAGING CELL FUNCTIONR01EY019587 · NEI · WASHINGTON UNIVERSITY · PI PIWNICA-WORMS, DAVID · 2009 to 2022
$5.3M
Immunodeficient Mouse Model of Stem Cell PlasticityR01DK061848 · NIDDK · WASHINGTON UNIVERSITY · PI NOLTA, JAN A. · 2001 to 2009
$2.7M
Functional dissection of human A-MSC vs BM-MSC phenotypeR01HL073256 · NHLBI · WASHINGTON UNIVERSITY · PI NOLTA, JAN A. · 2003 to 2010
$2.3M
EX VIVO STEM CELL MANIPULATION AND HUMAN HEMATOPOIESISR01DK053041 · NIDDK · WASHINGTON UNIVERSITY · PI NOLTA, JAN A. · 1998 to 2006
$1.6M
NCI NIH HHS P50 CA094056NCI NIH HHS P50-CA94056NEI NIH HHS R01 EY019587NHLBI NIH HHS R01 HL073256NHLBI NIH HHS R01HL073256NIDDK NIH HHS 2R01DK53041NIDDK NIH HHS 2R01DK61848NIDDK NIH HHS R01 DK053041NIDDK NIH HHS R01 DK061848
6 · The paper itself

Abstract

The use of nanometer-sized iron oxide particles combined with molecular imaging techniques enables dynamic studies of homing and trafficking of human hematopoietic stem cells (HSC). Identifying clinically applicable strategies for loading nanoparticles into primitive HSC requires strictly defined culture conditions to maintain viability without inducing terminal differentiation. In the current study, fluorescent molecules were covalently linked to dextran-coated iron oxide nanoparticles (Feridex) to characterize human HSC labeling to monitor the engraftment process. Conjugating fluorophores to the dextran coat for fluorescence-activated cell sorting purification eliminated spurious signals from nonsequestered nanoparticle contaminants. A short-term defined incubation strategy was developed that allowed efficient labeling of both quiescent and cycling HSC, with no discernable toxicity in vitro or in vivo. Transplantation of purified primary human cord blood lineage-depleted and CD34(+) cells into immunodeficient mice allowed detection of labeled human HSC in the recipient bones. Flow cytometry was used to precisely quantitate the cell populations that had sequestered the nanoparticles and to follow their fate post-transplantation. Flow cytometry endpoint analysis confirmed the presence of nanoparticle-labeled human stem cells in the marrow. The use of fluorophore-labeled iron oxide nanoparticles for fluorescence imaging in combination with flow cytometry allows evaluation of labeling efficiencies and homing capabilities of defined human HSC subsets.

Indexed as

Hematopoietic Stem Cell TransplantationIronOxidesAnimalsAntigens, CD34Cell CycleCell SurvivalColony-Forming Units AssayDextransFerrosoferric OxideFluorescent DyesGraft SurvivalHematopoietic Stem CellsHumansMagnetite NanoparticlesMetal NanoparticlesAntigens, CD34DextransFerrosoferric OxideferumoxidesFluorescent DyesIronMagnetite NanoparticlesOxides

Identifiers

PMID18055451
PMCPMC2863008
OpenAlexW2085068856

What OpenQuestion holds

Textmetadata
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.