An effective approach to cartilage regeneration using antler stem cell-conditioned medium
Zhou J., Xing B., Guo Q., Zhao J., Li X., Wang D.
Animal Study on Cartilage Damage, published in Sci Rep (2025) — summary generated from the PubMed abstract.
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
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
- Sci Rep (2025)
- Reported sample size
- —
- Source database
- Europe PMC
- PMID
- 40745014
- PMCID
- PMC12314024
- DOI
- 10.1038/s41598-025-13841-3
- Citations
- 2
Abstract (original English)
Articular cartilage has a low capacity for self-regeneration. Therefore, stem cell therapy has been proposed and is gaining momentum. Antler can self-repair and its cartilaginous tissue can grow at an unprecedented rate (Up to 2 cm/day) and antler regeneration is based on antler stem cells. Therefore, we predicted that antler stem cells or their paracrine factors might be a good source for promoting cartilage repair. In this study, we prepared conditioned medium from antler stem cells (ASC-CM) and evaluated its effect. We implanted the medium into rat cartilage defects and assessed its capacity to promote cartilage repair. The protein composition of ASC-CM was analyzed using via DIA assay. ASC-CM can strongly promote chondrocyte proliferation in vitro; it significantly up-regulates the expression of chondrogenesis-related genes (Aggrecan, Col II, and Sox-9) and promotes glycosaminoglycan formation and type II collagen deposition in cartilaginous tissue; meanwhile up-regulate the apoptosis suppressor gene NAMPT and down-regulate apoptosis gene BAX. In vivo, cartilage defect in rats was significantly repaired using ASC-CM. The compositions of ASC-CM were got and some key proteins such as S100A4 were identified by bioinformatics analysis. The ASC-CM can promote the proliferation of rat-chondrocytes, maintain the chondrocyte phenotype, and inhibit apoptosis of rat-chondrocytes. The
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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