Evidence map›Paper›PMID 24161166›Full record

ArticleBiomaterials2014

Promotion of airway anastomotic microvascular regeneration and alleviation of airway ischemia by deferoxamine nanoparticles.

Xinguo Jiang, Andrey V Malkovskiy, Wen Tian, Yon K Sung, Wenchao Sun, Joe L Hsu, Sathish Manickam, Dhananjay Wagh, Lydia-Marie Joubert, Gregg L Semenza and 2 more

Abstract read
In one paragraph

Article in Biomaterials, 2014. 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
1.7field-weighted citation impact, top 16% 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, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Deferoxamine Reduces Inflammation and Osteoclastogenesis in Avulsed Teeth.International journal of molecular sciences · 2021
    Article
  9. Article
  10. Nanoparticle Delivery Systems with Cell-Specific Targeting for Pulmonary Diseases.American journal of respiratory cell and molecular biology · 2021
    Review
  11. Article
  12. Review
  13. Endothelial HIF-2α as a Key Endogenous Mediator Preventing Emphysema.American journal of respiratory and critical care medicine · 2020
    Article
  14. Article
  15. Article
  16. Article
  17. Airway hypoxia in lung transplantation.Current opinion in physiology · 2019
    Article
  18. Article
  19. Hypoxia Signaling in Vascular Homeostasis.Physiology (Bethesda, Md.) · 2018
    Review
  20. A Modular Strategy to Engineer Complex Tissues and Organs.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2018
    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

12 authors at 3 institutions in 1 country.

Xinguo Jiang *Division of Pulmonary/Critical Care, Department of Medicine, VA Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA, USA.
Andrey V Malkovskiy *Stanford BioADD Laboratory, Stanford, CA, USA.
Wen TianDivision of Pulmonary/Critical Care, Department of Medicine, VA Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA, USA.
Yon K SungDivision of Pulmonary/Critical Care, Department of Medicine, VA Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA, USA.
Wenchao SunStanford BioADD Laboratory, Stanford, CA, USA.
Joe L HsuDivision of Pulmonary/Critical Care, Department of Medicine, VA Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA, USA.
Sathish ManickamStanford BioADD Laboratory, Stanford, CA, USA.
Dhananjay WaghStanford BioADD Laboratory, Stanford, CA, USA.
Lydia-Marie JoubertStanford Cell Sciences Imaging Facility, Stanford, CA, USA.
Gregg L SemenzaVascular Program, Institute for Cell Engineering, Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA.
Jayakumar RajadasStanford BioADD Laboratory, Stanford, CA, USA.
Mark R NicollsDivision of Pulmonary/Critical Care, Department of Medicine, VA Palo Alto Health Care System/Stanford University School of Medicine, Stanford, CA, USA.
VA Palo Alto Health Care System · USJohns Hopkins Medicine · USStanford University · US

Funding

The Cellular Response to Elafin in PAHP01HL108797 · NHLBI · STANFORD UNIVERSITY · PI NOLAN, GARRY P · 2011 to 2021
$19.7M
Critical Role for Microvasculature in Airway TransplantationR01HL095686 · NHLBI · PALO ALTO VETERANS INSTIT FOR RESEARCH · PI NICOLLS, MARK ROBERT · 2010 to 2022
$4.7M
The Role of Complement in Airway Microvascular DiseaseI01BX000509 · VA · VETERANS ADMIN PALO ALTO HEALTH CARE SYS · PI NICOLLS, MARK ROBERT · 2011 to 2013
–
BLRD VA I01 BX000509NHLBI NIH HHS HL095686NHLBI NIH HHS P01 HL108797NHLBI NIH HHS R01 HL095686
6 · The paper itself

Abstract

Airway tissue ischemia and hypoxia in human lung transplantation is a consequence of the sacrifice of the bronchial circulation during the surgical procedure and is a major risk factor for the development of airway anastomotic complications. Augmented expression of hypoxia-inducible factor (HIF)-1α promotes microvascular repair and alleviates allograft ischemia and hypoxia. Deferoxamine mesylate (DFO) is an FDA-approved iron chelator which has been shown to upregulate cellular HIF-1α. Here, we developed a nanoparticle formulation of DFO that can be topically applied to airway transplants at the time of surgery. In a mouse orthotopic tracheal transplant (OTT) model, the DFO nanoparticle was highly effective in enhancing airway microvascular perfusion following transplantation through the production of the angiogenic factors, placental growth factor (PLGF) and stromal cell-derived factor (SDF)-1. The endothelial cells in DFO treated airways displayed higher levels of p-eNOS and Ki67, less apoptosis, and decreased production of perivascular reactive oxygen species (ROS) compared to vehicle-treated airways. In summary, a DFO formulation topically-applied at the time of surgery successfully augmented airway anastomotic microvascular regeneration and the repair of alloimmune-injured microvasculature. This approach may be an effective topical transplant-conditioning therapy for preventing airway complications following clinical lung transplantation.

Indexed as

Angiogenesis Inducing AgentsAnimalsApoptosisChemokine CXCL12DeferoxamineEndothelial CellsHumansHypoxia-Inducible Factor 1, alpha SubunitIschemiaLung TransplantationMiceMice, Inbred BALB CMice, Inbred C57BLMicrovesselsNanoparticlesNitric Oxide Synthase Type IIIAngiogenesis Inducing AgentsChemokine CXCL12Cxcl12 protein, mouseDeferoxamineHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitNitric Oxide Synthase Type IIINos3 protein, mousePGF protein, humanPgf protein, mousePlacenta Growth FactorPregnancy ProteinsReactive Oxygen SpeciesBioabsorptionNanoparticleOxygenationSurface treatmentTransplantationWound healing

Identifiers

PMID24161166
PMCPMC4011640
OpenAlexW2106146695

What OpenQuestion holds

Textmetadata
LicenceTDM
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.