Cited by 103Mesenchymal stem cell researchBone Tissue Engineering MaterialsPeriodontal Regeneration and Treatments

The DOI matches its Crossref record; 60 of the 60 references it cites were found in a registry or an index.

Transplanted Umbilical Cord Mesenchymal Stem Cells Modify the In Vivo Microenvironment Enhancing Angiogenesis and Leading to Bone Regeneration

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Abstract

Umbilical cord mesenchymal stem cells (UC-MSCs) show properties similar to bone marrow mesenchymal stem cells (BM-MSCs), although controversial data exist regarding their osteogenic potential. We prepared clinical-grade UC-MSCs from Wharton's Jelly and we investigated if UC-MSCs could be used as substitutes for BM-MSCs in muscoloskeletal regeneration as a more readily available and functional source of MSCs. UC-MSCs were loaded onto scaffolds and implanted subcutaneously (ectopically) and in critical-sized calvarial defects (orthotopically) in mice. For live cell-tracking experiments, UC-MSCs were first transduced with the luciferase gene. Angiogenic properties of UC-MSCs were tested using the mouse metatarsal angiogenesis assay. Cell secretomes were screened for the presence of various cytokines using an array assay. Analysis of implanted scaffolds showed that UC-MSCs, contrary to BM-MSCs, remained detectable in the implants for 3 weeks at most and did not induce bone formation in an ectopic location. Instead, they induced a significant increase of blood vessel ingrowth. In agreement with these observations, UC-MSC-conditioned medium presented a distinct and stronger proinflammatory/chemotactic cytokine profile than BM-MSCs and a significantly enhanced angiogenic activity. When UC-MSCs were orthotopically transplanted in a calvarial defect, they promoted increased bone formation as well as BM-MSCs. However, at variance with BM-MSCs, the new bone was deposited through the activity of stimulated host cells, highlighting the importance of the microenvironment on determining cell commitment and response. Therefore, we propose, as therapy for bone lesions, the use of allogeneic UC-MSCs by not depositing bone matrix directly, but acting through the activation of endogenous repair mechanisms.

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Crossref · 10.1089/scd.2014.0490

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Research works printed but not linked: 2

  1. 1997, Adverse Drug React Toxicol Rev, 16, 113
  2. 10.1210/en.138.10.4456 · DOI

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Metadata

Authors
Todeschi, M. R., El Backly, R., Capelli, C., Daga, A., Patrone, E., Introna, M., Cancedda, R., & Mastrogiacomo, M.
Affiliations
  • University of Genoa (IT)
  • Department of Experimental Medicine (DIMES), University of Genoa, Genoa, Italy.
  • Ospedale Papa Giovanni XXIII (IT)
  • Ospedale Policlinico San Martino (IT)
Corresponding author
Mastrogiacomo, Maddalena
Venue
Stem Cells and Development
Published
2015-07
Volume
24
Issue
13
Pages
1570-1581
ISSN
  • 1525-8165 (ISSN-L)
  • 1547-3287
  • 1557-8534
OpenAlex
W2005472583
Cited by
103
References
60
Citations by year
2026: 3 · 2025: 4 · 2024: 6 · 2023: 11 · 2022: 10 · 2021: 7 · 2020: 12 · 2019: 14 · 2018: 10 · 2017: 12 · 2016: 9 · 2015: 5
FWCI
6.72
Type
journal article
Language
en
Open access
Locations
  • Stem Cells and Development (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • CINECA IRIS Institutial Research Information System (University of Genoa) (submittedVersion)
Funders
Regione Liguria
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Mesenchymal stem cell research
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Health Sciences › Dentistry › Periodontics › Periodontal Regeneration and Treatments
Keywords
human umbilical cord mesenchymal stem cells, Wharton's jelly, bone regeneration, angiogenesis, calvarial defect, bone marrow mesenchymal stem cells, cell microenvironment, secretome, inflammatory cytokines, cell tracking, allogeneic cell therapy, scaffold implantation
MeSH terms
Animals, Bone Regeneration, Cells, Cultured, Female, Humans, Umbilical Cord, Neovascularization, Physiologic, Mesenchymal Stem Cell Transplantation, Mice, Tissue Scaffolds, Stem Cell Niche, Mesenchymal Stem Cells

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