Evidence map›Paper›PMID 24386129›Full record

ArticlePloS one2013

Protective effects of mesenchymal stem cells with CXCR4 up-regulation in a rat renal transplantation model.

Zhiqiang Cao, Geng Zhang, Fuli Wang, Hongbao Liu, Long Liu, Yaling Han, Jian Zhang, Jianlin Yuan

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

21 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. CXCR4Stem cells international · 2022
    Article
  5. Review
  6. Review
  7. Review
  8. The Role of CXCL12 in Kidney Diseases: A Friend or Foe?Kidney diseases (Basel, Switzerland) · 2021
    Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
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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

8 authors at 3 institutions in 1 country.

Zhiqiang CaoDepartment of Urinary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Geng ZhangDepartment of Urinary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Fuli WangDepartment of Urinary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Hongbao LiuDepartment of Nephrology, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Long LiuLiaoning Province Translational Medicine Laboratory, Department of Urinary Urology and Cardiology of General Hospital of Shenyang Military Region, Shenyang, China.
Yaling HanDepartment of Urinary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China ; Liaoning Province Translational Medicine Laboratory, Department of Urinary Urology and Cardiology of General Hospital of Shenyang Military Region, Shenyang, China.
Jian ZhangState Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, Xi'an, China.
Jianlin YuanDepartment of Urinary Surgery, Xijing Hospital, Fourth Military Medical University, Xi'an, China.
Air Force Medical University · CNXijing Hospital · CNGeneral Hospital of Shenyang Military Region · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The homing of mesenchymal stem cells to injured tissue, which is important for the correction of conditions such as ischemia-reperfusion injury (IRI) and immunolesions, has been performed previously, but with poor efficiency. Substantial improvements in engraftment are required to derive clinical benefits from MSC transplantation. Chemokines are the most important factors that control cellular migration. Stromal derived factor-1 (SDF-1) is up-regulated during tissue/organ ischemia damage, and its cognate receptor, chemokine receptor 4 (CXCR4), is involved in stem cell migration. The aim of our study was to investigate CXCR4 expression in MSCs and to validate both its role in mediating migration to transplanted kidneys and its immunoregulatory effects in renal protection. Specifically, the present study was designed to investigate the short-term tissue homing of MSCs carrying genetically modified CXCR4 in a rat renal transplantation model. We tested the hypothesis that MSCs with CXCR4 over-expression can more efficiently regulate immunological reactions. Lentiviral vectors were used to over-express CXCR4 or to introduce a short hairpin ribonucleic acid (shRNA) construct targeting endogenous CXCR4 in rat MSCs. MSCs were labeled with enhanced green fluorescent protein (eGFP). After cell sorting, recipient kidneys were regionally perfused; recipient animals were injected with transduced MSCs, native MSCs, or PBS via tail vein following renal transplantation; and the effects of MSC injection were observed.

Indexed as

Mesenchymal Stem Cell TransplantationUp-RegulationAnimalsCell MovementChemokine CXCL12Graft RejectionGreen Fluorescent ProteinsKidney TransplantationModels, AnimalRatsReceptors, CXCR4TransplantsChemokine CXCL12CXCL12 protein, ratCxcr4 protein, ratGreen Fluorescent ProteinsReceptors, CXCR4

Identifiers

PMID24386129
PMCPMC3875425
OpenAlexW2042640240

What OpenQuestion holds

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LicenceCC BY
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.