Evidence map›Paper›PMID 17567755›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

IGF binding protein-3 regulates hematopoietic stem cell and endothelial precursor cell function during vascular development.

Kyung-Hee Chang, Tailoi Chan-Ling, Evan L McFarland, Aqeela Afzal, Hao Pan, Louise C Baxter, Lynn C Shaw, Sergio Caballero, Nilanjana Sengupta, Sergio Li Calzi and 2 more

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 88 papers.

0numbers the graph read from it
0cells of the map it votes in
88citing papers in PubMed
12.1field-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

88 citing papers in PubMed, 134 citations in OpenAlex.

  1. Trial
  2. IGFBP3 suppresses retinopathy through suppression of oxygen-induced vessel loss and promotion of vascular regrowth.Proceedings of the National Academy of Sciences of the United States of America · 2007
    Trial
  3. Article
  4. Review
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  6. The role of IGF/IGF-1R signaling in the regulation of cancer stem cells.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  7. Review
  8. Article
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  16. Article
  17. Review
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  19. Article
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28 more citing papers are in PubMed but not listed here.

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

12 authors at 3 institutions in 3 countries.

Kyung-Hee ChangProgram in Stem Cell Biology, University of Florida, Gainesville, FL 32610, USA.
Tailoi Chan-Ling
Evan L McFarland
Aqeela Afzal
Hao Pan
Louise C Baxter
Lynn C Shaw
Sergio Caballero
Nilanjana Sengupta
Sergio Li Calzi
Sean M Sullivan
Maria B Grant
University of Florida · USUniversity of Sydney · AUInstitute for Stem Cell Biology and Regenerative Medicine · IN

Funding

NITRIC OXIDE IN THE PATHOGENESIS OF DIABETIC RETINOPATHYR01EY012601 · NEI · UNIVERSITY OF FLORIDA · PI Julia V Busik, Maria Bartolomeo Grant · 1998 to 2026
$9.6M
Targeting the IGF-1 System in Retinal AngiogenesisR01EY007739 · NEI · UNIVERSITY OF FLORIDA · PI ABCOUWER, STEVEN F, GRANT, MARIA BARTOLOMEO · 1995 to 2015
$5.4M
HORMONES &NEOVASCULARIZATION IN DIABETIC RETINOPATHYR29EY007739 · NEI · UNIVERSITY OF FLORIDA · PI GRANT, MARIA B · 1989 to 1993
–
NEI NIH HHS EY007739NEI NIH HHS EY012601NEI NIH HHS R01 EY007739NEI NIH HHS R01 EY012601
6 · The paper itself

Abstract

We asked whether the hypoxia-regulated factor, insulin-like growth factor binding protein-3 (IGFBP3), could modulate stem cell factor receptor (c-kit+), stem cell antigen-1 (sca-1+), hematopoietic stem cell (HSC), or CD34+ endothelial precursor cell (EPC) function. Exposure of CD34+ EPCs to IGFBP3 resulted in rapid differentiation into endothelial cells and dose-dependent increases in cell migration and capillary tube formation. IGFBP3-expressing plasmid was injected into the vitreous of neonatal mice undergoing the oxygen-induced retinopathy (OIR) model. In separate studies, GFP-expressing HSCs were transfected with IGFBP3 plasmid and injected into the vitreous of OIR mice. Administering either IGFBP3 plasmid alone or HSCs transfected with the plasmid resulted in a similar reduction in areas of vasoobliteration, protection of the developing vasculature from hyperoxia-induced regression, and reduction in preretinal neovascularization compared to control plasmid or HSCs transfected with control plasmid. In conclusion, IGFBP3 mediates EPC migration, differentiation, and capillary formation in vitro. Targeted expression of IGFBP3 protects the vasculature from damage and promotes proper vascular repair after hyperoxic insult in the OIR model. IGFBP3 expression may represent a physiological adaptation to ischemia and potentially a therapeutic target for treatment of ischemic conditions.

Indexed as

AnimalsAnimals, NewbornAntigens, CD34Cell MovementCells, CulturedDose-Response Relationship, DrugEndothelial CellsGene Expression RegulationGreen Fluorescent ProteinsHematopoietic Stem CellsInjectionsInsulin-Like Growth Factor Binding Protein 3Lipopolysaccharide ReceptorsMiceMice, TransgenicNeovascularization, PhysiologicAntigens, CD34Green Fluorescent ProteinsInsulin-Like Growth Factor Binding Protein 3Lipopolysaccharide ReceptorsProto-Oncogene Proteins c-kit

Identifiers

PMID17567755
PMCPMC1965558
OpenAlexW2019329034

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.