Evidence map›Paper›PMID 21389314›Full record

ArticleBlood2011

Metabolic reprogramming by HIF-1 promotes the survival of bone marrow-derived angiogenic cells in ischemic tissue.

Sergio Rey, Weibo Luo, Larissa A Shimoda, Gregg L Semenza

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

33 citing papers in PubMed, 67 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Cardiomyocyte Maturation-the Road is not Obstructed.Stem cell reviews and reports · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Epigenetic crosstalk between hypoxia and tumor driven by HIF regulation.Journal of experimental & clinical cancer research : CR · 2020
    Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Systems biology of oxygen homeostasis.Wiley interdisciplinary reviews. Systems biology and medicine · 2017
    Review
  16. Review
  17. Targeting hypoxia-inducible factor 1 to stimulate tissue vascularization.Journal of investigative medicine : the official publication of the American Federation for Clinical Research · 2016
    Review
  18. Oxygen Sensing and Homeostasis.Physiology (Bethesda, Md.) · 2015
    Review
  19. Review
  20. Article
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

4 authors at 2 institutions in 1 country.

Sergio ReyInstitute for Cell Engineering, Johns Hopkins University Schoolof Medicine, Baltimore, MD, USA.
Weibo Luo
Larissa A Shimoda
Gregg L Semenza
Johns Hopkins University · USPulmonary and Critical Care Associates · US

Funding

HYPOXIA INDUCIBLE FACTOR I AND OXYGEN HOMEOSTASISR01HL055338 · NHLBI · JOHNS HOPKINS UNIVERSITY · PI SEMENZA, GREGG L · 1996 to 2009
$2.8M
NHLBI NIH HHS R01 HL055338NHLBI NIH HHS R01-HL55338
6 · The paper itself

Abstract

A major obstacle to using bone marrow cell-based therapies for ischemic cardiovascular disease is that transplanted cells must survive in an ischemic microenvironment characterized by low oxygen, glucose, and pH. We demonstrate that treatment of bone marrow-derived angiogenic cells (BMDACs) with dimethyloxalylglycine, an α-ketoglutarate antagonist that induces hypoxia-inducible factor 1 (HIF-1) activity, results in metabolic reprogramming of these cells, with increased glucose uptake, decreased O(2) consumption, increased lactate production, decreased reactive oxygen species, and increased intracellular pH. These effects are dependent on HIF-1, which transactivates target genes encoding metabolic enzymes and membrane transporters. Dimethyloxalylglycine-treated BMDACs have a significant survival advantage under conditions of low O(2) and low pH ex vivo and in ischemic tissue. Combined HIF-1α-based gene and cell therapy reduced tissue necrosis even when BMDAC donors and ischemic recipient mice were 17 months old, suggesting that this approach may have therapeutic utility in elderly patients with critical limb ischemia.

Indexed as

Neovascularization, PhysiologicAgingAmino Acids, DicarboxylicAnimalsBase SequenceBone Marrow CellsCell SurvivalDNA PrimersGlycolysisHumansHydrogen-Ion ConcentrationHypoxia-Inducible Factor 1, alpha SubunitIschemiaMaleMiceMice, 129 StrainAmino Acids, DicarboxylicDNA PrimersHif1a protein, mouseHypoxia-Inducible Factor 1, alpha Subunitoxalylglycine

Identifiers

PMID21389314
PMCPMC3100705
OpenAlexW2009621718

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.