Sustained adenosine release: Revealing its impact on osteogenic signalling pathways of human mesenchymal stromal cells

Q1 Medicine Engineered regeneration Pub Date : 2024-04-12 DOI:10.1016/j.engreg.2024.04.002
Hadi Hajiali , Jane McLaren , Cristina Gonzalez-García , Salah Abdelrazig , Dong-Hyun Kim , Matthew J. Dalby , Manuel Salmerón-Sánchez , Felicity R.A.J. Rose
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Abstract

Non-healing fractures, a global health concern arising from trauma, osteoporosis, and tumours, can lead to severe disabilities. Adenosine, integral to cellular energy metabolism, gains prominence in bone regeneration via adenosine A2B receptor activation. This study introduces a controlled-release system for localized adenosine delivery, fostering human mesenchymal stromal cell (hMSC) differentiation into functional bone cells. The study investigates how the ratio of lactic acid to glycolic acid in microparticles can influence adenosine release and explores the downstream effects on gene expression and metabolic profiles of osteogenic differentiation in hMSCs cultured in growth and osteoinductive media. Insights into adenosine-modulated signalling pathways during MSC differentiation, with osteogenic factors, provide a comprehensive understanding of the pathways involved. Analysing gene expression and metabolic profiles unravels adenosine's regulatory mechanisms in MSC differentiation. Sustained adenosine release from microparticles induces mineralization, synergizing with osteogenic media supplements, showcasing the potential of adenosine for treating critical bone defects and metabolic disorders. This study highlights the efficacy of a polymeric microparticle-based delivery system, offering novel strategies for bone repair. Unveiling adenosine's roles and associated signalling pathways advances our comprehension of molecular mechanisms steering bone regeneration, propelling innovative biomaterial, combined with metabolites, approaches for clinical use.

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持续腺苷释放:揭示其对人类间充质基质细胞成骨信号通路的影响
骨折不愈合是由创伤、骨质疏松症和肿瘤引起的全球性健康问题,可导致严重残疾。腺苷是细胞能量代谢不可或缺的物质,它通过腺苷 A2B 受体的激活在骨再生中发挥着重要作用。本研究介绍了一种用于局部递送腺苷的控释系统,可促进人间质基质细胞(hMSC)分化为功能性骨细胞。研究调查了微颗粒中乳酸和乙醇酸的比例如何影响腺苷的释放,并探讨了在生长和骨诱导培养基中培养的 hMSCs 成骨分化的基因表达和代谢谱的下游效应。该研究深入揭示了间充质干细胞分化过程中腺苷与成骨因子共同调控的信号通路,从而全面了解了相关通路。通过分析基因表达和新陈代谢图谱,揭示了腺苷在间充质干细胞分化过程中的调控机制。微颗粒持续释放腺苷可诱导矿化,与成骨培养基补充剂协同作用,展示了腺苷治疗严重骨缺损和代谢紊乱的潜力。这项研究强调了基于聚合物微粒的给药系统的功效,为骨修复提供了新的策略。揭示腺苷的作用和相关信号通路有助于我们理解引导骨再生的分子机制,推动创新生物材料与代谢物相结合的临床应用方法。
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来源期刊
Engineered regeneration
Engineered regeneration Biomaterials, Medicine and Dentistry (General), Biotechnology, Biomedical Engineering
CiteScore
22.90
自引率
0.00%
发文量
0
审稿时长
33 days
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