Evidence map›Paper›PMID 25351363›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2015

Mesenchymal stem cell expression of stromal cell-derived factor-1β augments bone formation in a model of local regenerative therapy.

Samuel Herberg, Galina Kondrikova, Khaled A Hussein, Maribeth H Johnson, Mohammed E Elsalanty, Xingming Shi, Mark W Hamrick, Carlos M Isales, William D Hill

Open access · greenAbstract readValidation Study
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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  3. Review
  4. Article
  5. Cxcl12 Deletion in Mesenchymal Cells Increases Bone Turnover and Attenuates the Loss of Cortical Bone Caused by Estrogen Deficiency in Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2020
    Article
  6. Article
  7. Article
  8. Review
  9. 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

9 authors at 3 institutions in 1 country.

Samuel HerbergDepartment of Biomedical Engineering, Case Western Reserve University, Cleveland, Ohio.
Galina Kondrikova
Khaled A Hussein
Maribeth H Johnson
Mohammed E Elsalanty
Xingming Shi
Mark W Hamrick
Carlos M Isales
William D Hill
Georgia Regents Medical Center · USAugusta University · USCase Western Reserve University · US

Funding

THE LEPTIN-IGF1 AXIS IN MUSCULOSKELETAL AGINGP01AG036675 · NIA · AUGUSTA UNIVERSITY · PI XINGMING SHI · 2011 to 2026
$31.5M
Bad to the Bone: Age-related Increases in Serum SDF-1 Leads to Bone Loss with AgeI01CX000930 · VA · RALPH H JOHNSON VA MEDICAL CENTER · PI HILL, WILLIAM D · 2014 to 2019
–
CSRD VA I01 CX000930NIA NIH HHS AG036675-01NIA NIH HHS P01 AG036675
6 · The paper itself

Abstract

Bone has the potential for spontaneous healing. However, this process often fails in patients with co-morbidities requiring clinical intervention. Numerous studies have revealed that bone marrow-derived mesenchymal stem/stromal cells (BMSCs) hold great potential for regenerative therapies. Common problems include poor cell engraftment, which can be addressed by irradiation prior to transplantation. Increasing evidence suggests that stromal cell-derived factor-1 (SDF-1) is involved in bone formation. However, osteogenic contributions of the beta splice variant of SDF-1 (SDF-1β), which is highly expressed in bone, remain unclear. Using the tetracycline (Tet)-regulatory system we have shown that SDF-1β enhances BMSC osteogenic differentiation in vitro. Here we test the hypothesis that SDF-1β augments bone formation in vivo in a model of local BMSC transplantation following irradiation. We found that SDF-1β, expressed at high levels in Tet-Off-SDF-1β BMSCs, augments the cell-mediated therapeutic effects resulting in enhanced bone formation, as evidenced by ex vivo μCT and bone histomorphometry. The data demonstrate the specific contribution of SDF-1β to BMSC-mediated bone formation, and validate the feasibility of the Tet-Off technology to regulate SDF-1β expression in vivo. In conclusion, SDF-1β provides potent synergistic effects supporting BMSC-mediated bone formation and appears a suitable candidate for optimization of bone augmentation in translational protocols.

Indexed as

Fracture HealingGenetic TherapyMesenchymal Stem Cell TransplantationOsteogenesisAnimalsBone TransplantationChemokine CXCL12MaleMice, Inbred C57BLTibiaChemokine CXCL12BMSCsbone formationirradiationSDF-1/CXCL12stem cell transplantation

Identifiers

PMID25351363
PMCPMC4706461
OpenAlexW1840439998

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.