Age-Related Changes in the Inflammatory Status of Human Mesenchymal Stem Cells: Implications for Cell Therapy

被引:56
作者
Zhang, Ying [1 ]
Ravikumar, Maanasa [1 ,2 ]
Ling, Ling [3 ]
Nurcombe, Victor [3 ,4 ]
Cool, Simon M. [1 ,2 ]
机构
[1] ASTAR, Inst Mol & Cell Biol, 61 Biopolis Dr, Singapore 138673, Singapore
[2] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Orthopaed Surg, Singapore 119288, Singapore
[3] ASTAR, Inst Med Biol, Singapore 138648, Singapore
[4] Nanyang Technol Univ Imperial Coll London, Lee Kong Chian Sch Med, Singapore 636921, Singapore
来源
STEM CELL REPORTS | 2021年 / 16卷 / 04期
关键词
PROLIFERATION IN-VITRO; VERSUS-HOST-DISEASE; BONE-MARROW; STROMAL CELLS; INDOLEAMINE 2,3-DIOXYGENASE; EXTRACELLULAR VESICLES; HEPARAN-SULFATE; SENESCENT CELLS; SURVIVAL; MSCS;
D O I
10.1016/j.stemcr.2021.01.021
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human mesenchymal stem/stromal cell (hMSC)-based cell therapies are promising for treating a variety of diseases. The unique immunomodulatory properties of hMSCs have extended their therapeutic potential beyond tissue regeneration. However, extensive pre-clinical culture expansion inevitably drives cells toward replicative ?aging?and a consequent decline in quality. These ?in vitro-aged?hMSCs resemble biologically aged cells, which have been reported to show senescence signatures, diminished immunosuppressive capacity, and weakened regenerative potential as well as pro-inflammatory features. In this review, we have surveyed the literature to explore the intimate relationship between the inflammatory status of hMSCs and their in vitro aging process. We posit that a shift from an anti-inflammatory to a pro-inflammatory phenotype of culture-expanded hMSCs contributes to a deterioration in their therapeutic efficacy. Potential molecular and cellular mechanisms underpinning this phenomenon have been discussed. We have also highlighted studies that leverage these mechanisms to make culture-expanded hMSCs more amenable for clinical use.
引用
收藏
页码:694 / 707
页数:14
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