Human Mesenchymal Stem Cell-Derived Extracellular Vesicles Promote Neural Differentiation of Neural Progenitor Cells

被引:16
作者
Park, So-Yeon [1 ,2 ]
Kim, Da-Seul [1 ,3 ]
Kim, Hyun-Mun [1 ]
Lee, Jun-Kyu [1 ]
Hwang, Dong-Youn [1 ]
Kim, Tae-Hyung [3 ]
You, Seungkwon [2 ]
Han, Dong Keun [1 ]
机构
[1] CHA Univ, Dept Biomed Sci, 335 Pangyo Ro, Seongnam Si 13488, South Korea
[2] Korea Univ, Coll Life Sci & Biotechnol, Div Biotechnol, Seoul 02841, South Korea
[3] Chung Ang Univ, Sch Integrat Engn, 84 Heukseok Ro, Seoul 06974, South Korea
基金
新加坡国家研究基金会;
关键词
extracellular vesicle (EV); mesenchymal stem cell; neural progenitor cell; neurogenesis; microRNA; cytokine; REGENERATION; SCAFFOLD; PROTEIN; INJURY;
D O I
10.3390/ijms23137047
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Mesenchymal stem cells (MSCs) have been adopted in various preclinical and clinical studies because of their multipotency and low immunogenicity. However, numerous obstacles relating to safety issues remain. Therefore, MSC-derived extracellular vesicles (EVs) have been recently employed. EVs are nano-sized endoplasmic reticulum particles generated and released in cells that have similar biological functions to their origin cells. EVs act as cargo for bioactive molecules such as proteins and genetic materials and facilitate tissue regeneration. EVs obtained from adipose-derived MSC (ADMSC) also have neuroprotective and neurogenesis effects. On the basis of the versatile effects of EVs, we aimed to enhance the neural differentiation ability of ADMSC-derived EVs by elucidating the neurogenic-differentiation process. ADMSC-derived EVs isolated from neurogenesis conditioned media (differentiated EVs, dEVs) increased neurogenic ability by altering innate microRNA expression and cytokine composition. Consequently, dEVs promoted neuronal differentiation of neural progenitor cells in vitro, suggesting that dEVs are a prospective candidate for EV-based neurological disorder regeneration therapy.
引用
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页数:12
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