Evidence map›Paper›PMID 21855069›Full record

ArticleAtherosclerosis2011

Impaired CXCR4 expression and cell engraftment of bone marrow-derived cells from aged atherogenic mice.

Qiyuan Xu, Jian'An Wang, Jinlin He, Mingsheng Zhou, Jennipher Adi, Keith A Webster, Hong Yu

Open access · greenAbstract read
In one paragraph

Article in Atherosclerosis, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.5field-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

14 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Review
  3. Role of Endothelial Progenitor Cells in Frailty.International journal of molecular sciences · 2023
    Review
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Review
  11. Review
  12. Review
  13. Review
  14. Regulation of atherogenesis by chemokines and chemokine receptors.Archivum immunologiae et therapiae experimentalis · 2013
    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

7 authors at 3 institutions in 2 countries.

Qiyuan XuDepartment of Cardiology, 2nd Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Jian'An Wang
Jinlin He
Mingsheng Zhou
Jennipher Adi
Keith A Webster
Hong Yu
Second Affiliated Hospital of Zhejiang University · CNUniversity of Miami · USSouth Florida Veterans Affairs Foundation for Research and Education · US

Funding

Regulated Therapeutic Angiogenesis: for Ischemic DiseaseR01HL072924 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WEBSTER, KEITH A · 2003 to 2014
$3.2M
JNK exacerbates ischemia/reperfusion injury in hyperglycemic subjects.R01HL092499 · NHLBI · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI WEBSTER, KEITH A · 2009 to 2010
$956k
NHLBI NIH HHS HL072924NHLBI NIH HHS HL092499NHLBI NIH HHS R01 HL072924NHLBI NIH HHS R01 HL092499
6 · The paper itself

Abstract

objectivesReduced numbers and activity of circulating progenitor cells are associated with aging and have been linked with coronary artery disease. To determine the impact of aging and atherosclerotic disease on the chemotaxic activity of bone marrow derived cells (BMCs), we examined CXCR4 surface expression on BMCs from aged and atherosclerotic mice.

methodsCXCR4 expression and cellular mobility were compared between BMCs of young (6-week old) ApoE null mice (ApoE(-/-)) and aged ApoE(-/-) mice that had been fed with a high-fat, high-cholesterol diet for 6-months.

resultsAge and atherosclerosis correlated with significantly lower surface expression of CXCR4 that was less inducible by calcium. The impaired calcium response was associated with defective calcium influx and was partially recovered by treatment with the calcium ionophore ionomycin. ApoE(-/-) mice fed high fat diet for 6-months had defective CXCR4 expression and SDF-1 regulation that is equivalent to that of 24-month old wild type mice. BMCs from aged, atherogenic ApoE(-/-) mice also displayed defective homing to SDF-1, and the animals had lower serum and bone marrow levels of SDF-1.

conclusionEvolution of atherosclerosis in ApoE(-/-) mice is paralleled by progressive loss of mobility of BMCs with reductions of CXCR4 expression, and reduced levels of SDF-1 in both serum and bone marrow. These changes mute the homing capability of BMCs and may contribute to the progression of atherosclerosis in this model.

Indexed as

AgingAnimalsApolipoproteins EApoptosisAtherosclerosisBone Marrow CellsCalciumCell MovementCell SurvivalChemokine CXCL12Diet, High-FatMiceMice, KnockoutReceptors, CXCR4Apolipoproteins ECalciumChemokine CXCL12Cxcl12 protein, mouseReceptors, CXCR4

Identifiers

PMID21855069
PMCPMC3206201
OpenAlexW2166877698

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.