Sigmarsdóttir Þóra, McGarrity Sarah, Rolfsson Óttar, Yurkovich James T, Sigurjónsson Ólafur E
The Blood Bank, Landspitali - The National University Hospital of Iceland, Reykjavik, Iceland.
School of Science and Engineering, Reykjavik University, Reykjavik, Iceland.
Front Bioeng Biotechnol. 2020 Mar 31;8:239. doi: 10.3389/fbioe.2020.00239. eCollection 2020.
Mesenchymal stem cells are a promising source for externally grown tissue replacements and patient-specific immunomodulatory treatments. This promise has not yet been fulfilled in part due to production scaling issues and the need to maintain the correct phenotype after re-implantation. One aspect of extracorporeal growth that may be manipulated to optimize cell growth and differentiation is metabolism. The metabolism of MSCs changes during and in response to differentiation and immunomodulatory changes. MSC metabolism may be linked to functional differences but how this occurs and influences MSC function remains unclear. Understanding how MSC metabolism relates to cell function is however important as metabolite availability and environmental circumstances in the body may affect the success of implantation. Genome-scale constraint based metabolic modeling can be used as a tool to fill gaps in knowledge of MSC metabolism, acting as a framework to integrate and understand various data types (e.g., genomic, transcriptomic and metabolomic). These approaches have long been used to optimize the growth and productivity of bacterial production systems and are being increasingly used to provide insights into human health research. Production of tissue for implantation using MSCs requires both optimized production of cell mass and the understanding of the patient and phenotype specific metabolic situation. This review considers the current knowledge of MSC metabolism and how it may be optimized along with the current and future uses of genome scale constraint based metabolic modeling to further this aim.
间充质干细胞是用于体外培养组织替代物和患者特异性免疫调节治疗的一种有前景的细胞来源。这一前景尚未完全实现,部分原因是生产规模扩大的问题以及重新植入后维持正确表型的需求。体外生长的一个可被操控以优化细胞生长和分化的方面是代谢。间充质干细胞的代谢在分化和免疫调节变化期间以及对这些变化的反应中会发生改变。间充质干细胞的代谢可能与功能差异相关,但这种关联如何发生以及如何影响间充质干细胞的功能仍不清楚。然而,了解间充质干细胞代谢与细胞功能的关系很重要,因为体内的代谢物可用性和环境状况可能会影响植入的成功率。基于基因组规模约束的代谢建模可作为一种工具来填补间充质干细胞代谢知识的空白,作为整合和理解各种数据类型(如基因组、转录组和代谢组)的框架。这些方法长期以来一直用于优化细菌生产系统的生长和生产力,并且越来越多地用于为人类健康研究提供见解。使用间充质干细胞生产用于植入的组织既需要优化细胞量的生产,也需要了解患者和表型特异性的代谢情况。本综述考虑了间充质干细胞代谢的现有知识以及如何对其进行优化,同时也探讨了基于基因组规模约束的代谢建模在当前和未来为实现这一目标的应用。