软骨发生
间充质干细胞
间质细胞
细胞生物学
祖细胞
软骨
化学
肌肉肥大
细胞
SMAD公司
再生(生物学)
细胞分化
干细胞
男科
转化生长因子
生物
医学
内分泌学
内科学
解剖
生物化学
基因
作者
Daniel S. Yang,Jay Trivedi,Daniel Betensky,Salomi Desai,Brett D. Owens,Chathuraka T. Jayasuriya
出处
期刊:Current stem cell research & therapy
[Bentham Science]
日期:2024-05-21
卷期号:19
标识
DOI:10.2174/011574888x314971240511151616
摘要
Introduction: Kartogenin (KGN) is a synthetic small molecule that stimulates chondrogenic cellular differentiation by activating smad-4/5 pathways. KGN has been proposed as a feasible alternative to expensive biologic growth factors, such as transforming growth factor β, which remain under strict regulatory scrutiny when it comes to use in patients. Method: This study reports the previously unexplored effects of KGN stimulation on cartilage- derived mesenchymal progenitor cells (CPCs), which have been shown to be effective in applications of cell-based musculoskeletal tissue regeneration. Our findings demonstrate that KGN treatment significantly increased markers of chondrogenesis, SOX9 and COL2 following 3-10 days of treatment in human CPCs. Result: KGN treatment also resulted in a significant dose-dependent increase in GAG production in CPCs. The same efficacy was not observed in human marrow-derived stromal cells (BM-MSCs); however, KGN significantly reduced mRNA expression of cell hypertrophy markers, COL10 and MMP13, in BM-MSCs. Parallel to these mRNA expression results, KGN led to a significant decrease in protein levels of MMP-13 both at 0-5 days and 5-10 days following KGN treatment. Conclusion: In conclusion, this study demonstrates that KGN can boost the chondrogenicity of CPCs and inhibit hypertrophic terminal differentiation of BM-MSCs.
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