循环祖细胞是软骨形成和成骨的重要生物标志物:在诊断和治疗随访中的应用

M. Valenti, M. Mottes, L. Carbonare
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引用次数: 0

摘要

成体多能间充质干细胞(MSCs)具有许多可能的临床应用,引起了人们极大的科学兴趣。除了组织再生和修复的治疗潜力外,它们还提供了作为诊断工具的新机会。出于诊断目的,外周血是循环MSC的一种容易获得的来源,与骨髓MSC相比,循环MSC表现出相似的特征。骨髓间充质干细胞的软骨和成骨分化功能障碍与骨关节炎和骨质疏松等年龄相关性退行性疾病的发生有关。可以在患者外周血MSC的离体分析中监测特定转录因子的表达谱的改变;它们代表了诊断的重要生物标志物。此外,药物治疗诱导的MSCs表达谱的变化是治疗随访的有用生物标志物。微小RNA在祖细胞的软骨和成骨分化中也起着至关重要的作用;差异表达的微小RNA已分别与骨关节炎和骨质疏松症相关。微小核糖核酸可以从血液、尿液和滑液中回收,是诊断这些退行性疾病的有用补充工具。总之,循环MSC可以通过非侵入性方法获得,并为监测正常和病理条件下的各种分化途径提供“离体”来源;因此,它们代表了用于各种临床应用的显著资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Circulating progenitor stem cells are important biomarkers of chondrogenesis and osteogenesis: employment in diagnosis and treatment follow up
Adult multipotent mesenchymal stem cells (MSCs) arouse great scientific interest because of their many possible clinical applications. Besides the therapeutic potential for tissue regeneration and repair, they also offer new opportunities as diagnostic tools. For diagnostic purposes peripheral blood represents an easily accessible source of circulating MSCs which show similar characteristics compared to bone marrow MSCs. Dysfunctions in chondrogenic and osteogenic differentiation of MSCs are involved in the genesis of age-related degenerative disorders as osteoarthritis and osteoporosis. Altered expression profiles of specific transcription factors may be monitored in the ex vivo analysis of patients’ peripheral blood MSCs; they represent important biomarkers for diagnosis. Furthermore, changes in MSCs expression profiles induced by pharmacological treatments are useful biomarkers for therapy followup. MicroRNAs also play a crucial role in chondrogenic and osteogenic differentiation of progenitor cells; differentially expressed microRNAs have been associated with osteoarthritis and osteoporosis, respectively. MicroRNAs can be recovered from blood, urine, and synovial fluid and represent useful supplemental tools for the diagnosis of these degenerative disorders. In conclusion, circulating MSCs can be obtained by a non-invasive approach and provide an “ex vivo” source for monitoring various differentiation pathways in normal and pathological conditions; thus they represent a remarkable resource for various clinical applications.
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