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鉴定成骨潜能分析的生物标志物。

Identifying Biomarkers for Osteogenic Potency Assay Development.

机构信息

Department of Environmental and Prevention Sciences, University of Ferrara, Ferrara, Italy.

University Hospital of Odense, University of Southern Denmark, Odense, Denmark.

出版信息

Adv Exp Med Biol. 2023;1420:39-58. doi: 10.1007/978-3-031-30040-0_4.

Abstract

There has been extensive exploration of how cells may serve as advanced therapy medicinal products to treat skeletal pathologies. Osteoblast progenitors responsible for production of extracellular matrix that is subsequently mineralized during bone formation have been characterised as a rare bone marrow subpopulation of cell culture plastic adherent cells. Conveniently, they proliferate to form single-cell derived colonies of fibroblastoid cells, termed colony forming unit fibroblasts that can subsequently differentiate to aggregates resembling small areas of cartilage or bone. However, donor heterogeneity and loss of osteogenic differentiation capacity during extended cell culture have made the discovery of reliable potency assay biomarkers difficult. Nonetheless, functional osteoblast models derived from telomerised human bone marrow stromal cells have allowed extensive comparative analysis of gene expression, microRNA, morphological phenotypes and secreted proteins. This chapter highlights numerous insights into the molecular mechanisms underpinning osteogenic differentiation of multipotent stromal cells and bone formation, discussing aspects involved in the choice of useful biomarkers for functional attributes that can be quantitively measured in osteogenic potency assays.

摘要

人们对细胞如何作为治疗骨骼疾病的高级治疗药物进行了广泛的探索。成骨细胞祖细胞负责产生细胞外基质,随后在骨形成过程中矿化,已被描述为骨髓细胞培养塑料贴壁细胞的稀有亚群。方便的是,它们增殖形成单个细胞衍生的成纤维细胞集落,称为成纤维细胞集落形成单位,随后可分化为类似于小块软骨或骨的聚集物。然而,供体异质性和细胞培养过程中骨生成分化能力的丧失使得发现可靠的效力测定生物标志物变得困难。尽管如此,源自端粒化人骨髓基质细胞的功能性成骨细胞模型允许对基因表达、microRNA、形态表型和分泌蛋白进行广泛的比较分析。本章重点介绍了对多能基质细胞成骨分化和骨形成的分子机制的许多深入了解,讨论了在选择有用的生物标志物方面的一些内容,这些生物标志物可用于在成骨效力测定中定量测量功能属性。

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