Evidence map›Paper›PMID 21499736›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2011

Aging impairs the mobilization and homing of bone marrow-derived angiogenic cells to burn wounds.

Xianjie Zhang, Kakali Sarkar, Sergio Rey, Raul Sebastian, Efstathia Andrikopoulou, Guy P Marti, Karen Fox-Talbot, Gregg L Semenza, John W Harmon

Abstract read
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

28 citing papers in PubMed, 56 citations in OpenAlex.

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  12. Uniquely human CHRFAM7A gene increases the hematopoietic stem cell reservoir in mice and amplifies their inflammatory response.Proceedings of the National Academy of Sciences of the United States of America · 2019
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  20. Hypoxic signaling during tissue repair and regenerative medicine.International journal of molecular sciences · 2014
    Review
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 3 institutions in 1 country.

Xianjie ZhangHendrix Burn Laboratory, Department of Surgery, Johns Hopkins Bayview Medical Center, Baltimore, MD 21224, USA.
Kakali Sarkar
Sergio Rey
Raul Sebastian
Efstathia Andrikopoulou
Guy P Marti
Karen Fox-Talbot
Gregg L Semenza
John W Harmon
Johns Hopkins University · USJohns Hopkins Bayview Medical Center · USJohns Hopkins Medicine · US

Funding

HIF-1-Regulated Endothelial Progenitor Cell Recruitment in Burn Wound HealingP20GM078494 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI SEMENZA, GREGG L · 2006 to 2010
$3.3M
NIGMS NIH HHS P20 GM078494NIGMS NIH HHS P20-GM078494
6 · The paper itself

Abstract

Impaired wound healing in the elderly represents a major clinical problem. Delineating the cellular and molecular mechanisms by which aging impairs wound healing may lead to the development of improved treatment strategies for elderly patients with non-healing wounds. Neovascularization is an essential step in wound healing, and bone marrow-derived angiogenic cells (BMDACs) play an important role in vascularization. Using a mouse full-thickness burn wound model, we demonstrate that perfusion and vascularization of burn wounds were impaired by aging and were associated with dramatically reduced mobilization of BMDACs bearing the cell surface molecules CXCR4 and Sca1. Expression of stromal-derived factor 1 (SDF-1), the cytokine ligand for CXCR4, was significantly decreased in peripheral blood and burn wounds of old mice. Expression of hypoxia-inducible factor (HIF)-1α was detected in burn wounds from young (2-month-old), but not old (2-year-old), mice. When BMDACs from young donor mice were injected intravenously, homing to burn wound tissue was impaired in old recipient mice, whereas the age of the BMDAC donor mice had no effect on homing. Our results indicate that aging impairs burn wound vascularization by impairing the mobilization of BMDACs and their homing to burn wound tissue as a result of impaired HIF-1 induction and SDF-1 signaling.

Indexed as

Cell MovementNeovascularization, PhysiologicWound HealingAgingAnimalsBone Marrow CellsBurnsCell CountChemokine CXCL12Gene Expression RegulationHypoxia-Inducible Factor 1, alpha SubunitMaleMiceMice, Inbred C57BLModels, BiologicalPerfusionChemokine CXCL12Hypoxia-Inducible Factor 1, alpha Subunit

Identifiers

PMID21499736
PMCPMC3587336
OpenAlexW2004857262

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.