Level D· Scientific groundwork from lab and animal studiesAnimal StudyEurope PMCOpen access

Effects of basic fibroblast growth factor on cartilage to bone: Time-course histological analysis of in vivo cartilage formation from polydactyly-derived chondrocytes

Nasu M., Takayama S., Amagase R., Umezawa A.

Animal Study on Scar, published in Regen Ther (2025) — summary generated from the PubMed abstract.

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Level D· Scientific groundwork from lab and animal studiesEvidence level of this study

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

  • Level A · Stronger Clinical Evidence
  • Level B · Emerging clinical evidence with positive signals
  • Level C · Early human research exploring benefits
  • Level D · Scientific groundwork from lab and animal studies
  • Emerging · Emerging topic under active research
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This page is generated from the PubMed record. The Thai description is an automated summary of bibliographic fields and the abstract, not a full translation, and is not medical advice.

Study type
Animal Study
Journal
Regen Ther (2025)
Reported sample size
—
Source database
Europe PMC
PMID
39967783
PMCID
PMC11833415
DOI
10.1016/j.reth.2025.01.013
Citations
1

Abstract (original English)

Introduction Cartilage tissue is important in the human body as a ubiquitous connective tissue. However, information on the limits of chondrocyte growth and the effects of basic FGF (bFGF) in vivo is scarce. This study aims to investigate the effects of bFGF on the growth rate, cytology, and morphology of implanted cultured epiphyseal cartilage-derived chondrocytes into NOD/Shi-scid IL-2Rγ null mice (NOG mice). Methods Chondrocytes were isolated from the epiphyseal cartilage derived from the digits of polydactyly patients and were cultivated in a medium supplemented with bFGF (bFGF-treated cells) and without bFGF (bFGF-untreated cells). These cultivated cells were subcutaneously implanted into the backs of NOG mice. Results bFGF-treated cells exhibited a higher growth rate than bFGF-untreated cells. Cartilage was formed after two weeks of implantation. The cartilages generated by bFGF-treated cells (denoted as "BT-cartilage" hereafter) were larger in size and heavier in weight than those cartilages generated by bFGF-untreated cells (denoted as "BUT-cartilage" hereafter). BT-cartilage grew exponentially after 10 weeks. Conclusions From these results, bFGF-treated cells exhibited increased ability for both proliferation and differentiation compared to bFGF-untreated cells. The results of this study may lead to the generation of new alternative therapies for bone and cartilage thr

What this study does not prove

  • • This study does not prove SVF is an approved treatment or a replacement for standard care.
  • • This is preclinical work; animal or laboratory results cannot be applied to humans.

Evidence level

Evidence from laboratory and animal studies provides groundwork for understanding mechanisms and potential before human studies continue.

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