Mesenchymal stem cells as a potential therapeutic tool to cure cognitive impairment caused by neuroinflammation

被引:22
作者
Skok, Maryna [1 ]
机构
[1] NAS Ukraine, Dept Mol Immunol, Palladin Inst Biochem, 9 Leontovicha str, UA-01054 Kiev, Ukraine
来源
WORLD JOURNAL OF STEM CELLS | 2021年 / 13卷 / 08期
关键词
Mesenchymal stem cells; Neuroinflammation; Cognition; alpha 7 Nicotinic acetylcholine receptor; Extracellular vesicles; Alzheimer disease; NICOTINIC ACETYLCHOLINE-RECEPTOR; AMYLOID-BETA DEPOSITION; ALZHEIMERS-DISEASE; BONE-MARROW; INTRACEREBRAL TRANSPLANTATION; PARKINSONS-DISEASE; RAT MODEL; IN-VITRO; BRAIN; MICROGLIA;
D O I
10.4252/wjsc.v13.i8.1072
中图分类号
Q813 [细胞工程];
学科分类号
摘要
An established contribution of neuroinflammation to multiple brain pathologies has raised the requirement for therapeutic strategies to overcome it in order to prevent age- and disease-dependent cognitive decline. Mesenchymal stem cells (MSCs) produce multiple growth and neurotrophic factors and seem to evade immune rejection due to low expression of major histocompatibility complex class I molecules. Therefore, MSCs are widely used in experiments and clinical trials of regenerative medicine. This review summarizes recent data concerning the optimization of MSC use for therapeutic purposes with the emphasis on the achievements of the last 2 years. Specific attention is paid to extracellular vesicles secreted by MSCs and to the role of alpha 7 nicotinic acetylcholine receptors. The reviewed data demonstrate that MSCs have a significant therapeutic potential in treating neuroinflammation-related cognitive disfunctions including age-related neurodegenerative diseases. The novel data demonstrate that maximal therapeutic effect is being achieved when MSCs penetrate the brain and produce their stimulating factors in situ. Consequently, therapeutic application using MSCs should include measures to facilitate their homing to the brain, support the survival in the brain microenvironment, and stimulate the production of neurotrophic and anti-inflammatory factors. These measures include but are not limited to genetic modification of MSCs and pre-conditioning before transplantation.
引用
收藏
页码:1072 / 1083
页数:12
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