In vitro augmentation of mesenchymal stem cells viability in stressful microenvironments

被引:96
作者
Amiri, Fatemeh [1 ]
Jahanian-Najafabadi, Ali [2 ]
Roudkenar, Mehryar Habibi [1 ]
机构
[1] High Inst Res & Educ Transfus Med, Blood Transfus Res Ctr, Tehran, Iran
[2] Isfahan Univ Med Sci & Hlth Serv, Sch Pharm, Dept Pharmaceut Biotechnol, Esfahan, Iran
关键词
Mesenchymal stem cell; Preconditioning; Scaffold; Conditioned medium; Microenvironment; Bioreactor; LEVEL LASER IRRADIATION; MARROW STROMAL CELLS; BONE-MARROW; UMBILICAL-CORD; ADIPOSE-TISSUE; INDUCED APOPTOSIS; OXIDATIVE STRESS; PROGENITOR CELLS; CULTURE-CONDITIONS; SERUM DEPRIVATION;
D O I
10.1007/s12192-014-0560-1
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Mesenchymal stem cells (MSCs) are under intensive investigation for use in cell-based therapies because their differentiation abilities, immunomodulatory effects, and homing properties offer potential for significantly augmenting regenerative capacity of many tissues. Nevertheless, major impediments to their therapeutic application, such as low proliferation and survival rates remain as obstacles to broad clinical use of MSCs. Another major challenge to evolution of MSC-based therapies is functional degradation of these cells as a result of their exposure to oxidative stressors during isolation. Indeed, oxidative stress-mediated MSC depletion occurs due to inflammatory processes associated with chemotherapy, radiotherapy, and expression of pro-apoptotic factors, and the microenvironment of damaged tissue in patients receiving MSC therapy is typically therapeutic not favorable to their survival. For this reason, any strategies that enhance the viability and proliferative capacity of MSCs associated with their therapeutic use are of great value. Here, recent strategies used by various researchers to improve MSC allograft function are reviewed, with particular focus on in vitro conditioning of MSCs in preparation for clinical application. Preconditioning, genetic manipulation, and optimization of MSC culture conditions are some examples of the methodologies described in the present article, along with novel strategies such as treatment of MSCs with secretome and MSC-derived microvesicles. This topic material is likely to find value as a guide for both research and clinical use of MSC allografts and for improvement of the value that use of these cells brings to health care.
引用
收藏
页码:237 / 251
页数:15
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