Time-Dependent Anabolic Response of hMSC-Derived Cartilage Grafts to Hydrostatic Pressure

IF 3.1 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Farhad Chariyev-Prinz, N. Neto, M. Monaghan, D. Kelly
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引用次数: 0

Abstract

It is generally accepted that the application of hydrostatic pressure (HP) is beneficial for MSC chondrogenesis. There is, however, evidence to suggest that the timing of application might determine its impact on cell fate and tissue development. Furthermore, understanding how the maturity of engineered cartilage affects its response to the application of HP can provide critical insight into determining when such a graft is ready for in vivo implantation into a mechanically loaded environment. In this study, we systematically examined chondrogenic maturation of hMSCs over 35 days in the presence of TGF-β3 in vitro. At specific timepoints, the response of hMSCs to the application of HP following the removal of TGF-β3 was assessed; this partially models conditions such grafts will experience in vivo upon implantation. In free swelling culture, the expression of chondrogenic (COL2A1 and ACAN) and hypertrophic (COL10A1) markers increased with time. At early timepoints, the expression of such markers continued to increase following TGF-β3 withdrawal; however, this was not observed after prolonged periods of chondrogenic priming (35 days). Interestingly, the application of HP was only beneficial after 35 days of chondrogenic priming, where it enhanced sGAG synthesis and improved key chondrogenic gene ratios. It was also found that HP can facilitate a metabolic shift towards oxidative phosphorylation, which can be viewed as a hallmark of successfully differentiating MSCs. These results point to the importance of mechanical loading as a key stimulus for maintaining a chondrogenic phenotype once MSCs are removed from chemically defined culture conditions.
hmsc衍生软骨移植物对静水压力的合成代谢响应
人们普遍认为,应用静水压(HP)有利于MSC软骨形成。然而,有证据表明,应用的时间可能决定其对细胞命运和组织发育的影响。此外,了解工程软骨的成熟度如何影响其对HP应用的反应,可以为确定这种移植物何时准备好在体内植入机械负载环境提供关键见解。在这项研究中,我们系统地检测了35岁以上hMSCs的软骨形成成熟度 在体外TGF-β3存在下的天数。在特定时间点,评估hMSCs在去除TGF-β3后对HP应用的反应;这部分模拟了这种移植物在植入时将在体内经历的条件。在自由肿胀培养中,软骨生成(COL2A1和ACAN)和肥大(COL10A1)标志物的表达随着时间的推移而增加。在早期,TGF-β3退出后,这些标志物的表达继续增加;然而,在长时间的软骨原性启动后没有观察到这种情况(35 天)。有趣的是,HP的应用仅在35岁后才有益 几天的软骨形成启动,在那里它增强了sGAG的合成并提高了关键的软骨形成基因比率。研究还发现,HP可以促进代谢向氧化磷酸化的转变,这可以被视为成功分化MSCs的标志。这些结果表明,一旦MSCs从化学定义的培养条件中去除,机械负载作为维持软骨形成表型的关键刺激的重要性。
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来源期刊
CiteScore
7.50
自引率
3.00%
发文量
97
审稿时长
4-8 weeks
期刊介绍: Journal of Tissue Engineering and Regenerative Medicine publishes rapidly and rigorously peer-reviewed research papers, reviews, clinical case reports, perspectives, and short communications on topics relevant to the development of therapeutic approaches which combine stem or progenitor cells, biomaterials and scaffolds, growth factors and other bioactive agents, and their respective constructs. All papers should deal with research that has a direct or potential impact on the development of novel clinical approaches for the regeneration or repair of tissues and organs. The journal is multidisciplinary, covering the combination of the principles of life sciences and engineering in efforts to advance medicine and clinical strategies. The journal focuses on the use of cells, materials, and biochemical/mechanical factors in the development of biological functional substitutes that restore, maintain, or improve tissue or organ function. The journal publishes research on any tissue or organ and covers all key aspects of the field, including the development of new biomaterials and processing of scaffolds; the use of different types of cells (mainly stem and progenitor cells) and their culture in specific bioreactors; studies in relevant animal models; and clinical trials in human patients performed under strict regulatory and ethical frameworks. Manuscripts describing the use of advanced methods for the characterization of engineered tissues are also of special interest to the journal readership.
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