Khan Hiba, Mafi Pouya, Mafi Reza, Khan Wasim
Hull York Medical School, Cottingham Road, Hull, HU6 7RX, United Kingdom.
Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, OX3 7LD, United Kingdom.
Curr Stem Cell Res Ther. 2018;13(5):378-383. doi: 10.2174/1574888X11666160429122527.
BACKGROUND: Mesenchymal stem cells (MSC) are unique in their ability to self-renew and differentiate into one of many lineage possibilities. It is therefore integral to preserve these qualities to prevent the far reaching effects of a defective stem cell. Human mesenchymal stem cells (hMSC) are precursors for and can differentiate into osteoblasts, adipocytes and chondrocytes. They were originally found in the bone marrow, but have also been located in the umbilical cord, adipose tissue and muscle. Few studies have been conducted into the in vivo effects of age on these cells. This contribution reviews current knowledge surrounding the effects of age on the characteriation and differentiation of human mesenchymal stem cells. METHOD: 471 articles were found using a combination of Online published articles from January 1983 to January 2016 were searched using the Cochrane Library, PubMed, Medline, Scopus, Web of Science and Science Direct databases. There were no existing systematic reviews on this research topic. RESULTS: Nine studies were identified that met the predefined selection criteria. Three studies were used to assess the effects of ageing on characterisation of hMSC with no conclusive results. The cumulative results of these studies show that the effect of ageing on characterisation of hMSC remains inconclusive. Seven studies were used to assess the differentiation potentials of hMSC showing that age either decreased or altered lineage preference in hMSC differentiation. CONCLUSION: There is indication that ageing affects hMSC characterisation and differentiation, however it is not conclusive. There are not enough high quality controlled clinical trials to make reliable conclusions.
背景:间充质干细胞(MSC)具有自我更新和分化为多种谱系细胞的独特能力。因此,保持这些特性对于防止有缺陷的干细胞产生深远影响至关重要。人骨髓间充质干细胞(hMSC)是成骨细胞、脂肪细胞和软骨细胞的前体细胞,能够分化为这些细胞。它们最初在骨髓中被发现,但也存在于脐带、脂肪组织和肌肉中。关于年龄对这些细胞的体内影响的研究较少。本文综述了目前关于年龄对人骨髓间充质干细胞特征和分化影响的相关知识。 方法:通过使用Cochrane图书馆、PubMed、Medline、Scopus、科学网和科学直达数据库,检索了1983年1月至2016年1月在线发表的文章,共找到471篇文章。关于该研究主题尚无现有的系统评价。 结果:确定了9项符合预定义选择标准的研究。3项研究用于评估衰老对hMSC特征的影响,结果尚无定论。这些研究的累积结果表明,衰老对hMSC特征的影响仍无定论。7项研究用于评估hMSC的分化潜能,结果表明年龄会降低或改变hMSC分化中的谱系偏好。 结论:有迹象表明衰老会影响hMSC的特征和分化,但尚无定论。没有足够高质量的对照临床试验来得出可靠的结论。
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