Mesenchymal stem cell-derived exosomes as a bioinspired nanoscale tool toward next-generation cell-free treatment

被引:7
作者
Asadi, Khatereh [1 ,2 ]
Amini, Abbas [3 ,4 ]
Gholami, Ahmad [5 ,6 ,7 ]
机构
[1] Shiraz Univ Med Sci, Biotechnol Res Ctr, Shiraz, Iran
[2] Guilan Univ Med Sci, Guilan Rd Trauma Res Ctr, Rasht, Iran
[3] Australian Univ Kuwait, Dept Mech Engn, Kuwait 13015, Kuwait
[4] Western Sydney Univ, Ctr Infrastruct Engn, Kingswood, NSW, Australia
[5] Shiraz Univ Med Sci, Pharmaceut Sci Res Ctr, Shiraz, Iran
[6] Shiraz Univ Med Sci, Sch Adv Med Sci & Technol, Dept Med Nanotechnol, Shiraz, Iran
[7] Shiraz Univ Med Sci, POB 71345-1583, Shiraz, Iran
关键词
Mesenchymal stem cell; Exosome; Isolation; Fabrication; Cargo loading; DRUG-DELIVERY;
D O I
10.1016/j.jddst.2022.103856
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background: Mesenchymal stem cells derived exosomes (MSCs-exosomes) with intrinsic dominance bioinspired nanoscale tools to produce efficient biological compounds based on nanotechnology and biotechnology combinations for clinical use.Main text: MSCs-exosomes with the vesicular bilayer structure are enriched with many proteins, nucleic acids, and lipids that modulate a wide range of biological phenomena and provide various substances for incorporation. Novel modification approaches look viable to assess their target site delivery, intracellular communications, and half-life. Various endeavors have been made to develop efficient production, purification, and functionalization techniques as a straightforward avenue to achieve effective targeted delivery. Moreover, the progress of standard analytical tools could bring exosome products from the bench to the bedside. Furthermore, MSCs-exosomes are expected to be the next generation of cell-free treatments applied to most human pathologic conditions.Conclusion: MSCs-exosomes encompass parental cells' crucial paracrine functions instead of using cells as therapeutic agents. This review mentioned all aspects of MSCs-exosomes isolation, encapsulation, modification strategies, regulations, and the recent research progress in various diseases of MSC-exosomes.
引用
收藏
页数:13
相关论文
共 92 条
[11]   Exosome/microvesicle content is altered in leucine-rich repeat kinase 2 mutant induced pluripotent stem cell-derived neural cells [J].
Candelario, Kate M. ;
Balaj, Leonora ;
Zheng, Tong ;
Skog, Johan ;
Scheffler, Bjorn ;
Breakefield, Xandra ;
Schule, Birgitt ;
Steindler, Dennis A. .
JOURNAL OF COMPARATIVE NEUROLOGY, 2020, 528 (07) :1203-1215
[12]   Exosomes, a New Star for Targeted Delivery [J].
Chen, Huizhi ;
Wang, Liyan ;
Zeng, Xinling ;
Schwarz, Herbert ;
Nanda, Himansu Sekhar ;
Peng, Xinsheng ;
Zhou, Yubin .
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY, 2021, 9
[13]   Human umbilical cord-derived mesenchymal stem cell-exosomal miR-627-5p ameliorates non-alcoholic fatty liver disease by repressing FTO expression [J].
Cheng, Lidan ;
Yu, Peng ;
Li, Fangfang ;
Jiang, Xueling ;
Jiao, Xiaojuan ;
Shen, Yunfeng ;
Lai, Xiaoyang .
HUMAN CELL, 2021, 34 (06) :1697-1708
[14]   Biodistribution of Exosomes and Engineering Strategies for Targeted Delivery of Therapeutic Exosomes [J].
Choi, Hojun ;
Choi, Yoorim ;
Yim, Hwa Young ;
Mirzaaghasi, Amin ;
Yoo, Jae-Kwang ;
Choi, Chulhee .
TISSUE ENGINEERING AND REGENERATIVE MEDICINE, 2021, 18 (04) :499-511
[15]   Novel versatile 3D bio-scaffold made of natural biocompatible hagfish exudate for tissue growth and organoid modeling [J].
Dastjerdi, Mahsa Borzouyan ;
Amini, Abbas ;
Nazari, Marziyeh ;
Cheng, Chun ;
Benson, Veronika ;
Gholami, Ahmad ;
Ghasemi, Younes .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 2020, 158 :894-902
[16]   Photoreceptor protection by mesenchymal stem cell transplantation identifies exosomal MiR-21 as a therapeutic for retinal degeneration [J].
Deng, Chun-Lei ;
Hu, Cheng-Biao ;
Ling, Sheng-Tao ;
Zhao, Na ;
Bao, Li-Hui ;
Zhou, Feng ;
Xiong, Ye-Cheng ;
Chen, Tao ;
Sui, Bing-Dong ;
Yu, Xiao-Rui ;
Hu, Cheng-Hu .
CELL DEATH AND DIFFERENTIATION, 2021, 28 (03) :1041-1061
[17]   Mesenchymal Stem/Stromal Cell Therapy in Blood-Brain Barrier Preservation Following Ischemia: Molecular Mechanisms and Prospects [J].
Do, Phuong Thao ;
Wu, Chung-Che ;
Chiang, Yung-Hsiao ;
Hu, Chaur-Jong ;
Chen, Kai-Yun .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2021, 22 (18)
[18]   Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement [J].
Dominici, M. ;
Le Blanc, K. ;
Mueller, I. ;
Slaper-Cortenbach, I. ;
Marini, F. C. ;
Krause, D. S. ;
Deans, R. J. ;
Keating, A. ;
Prockop, D. J. ;
Horwitz, E. M. .
CYTOTHERAPY, 2006, 8 (04) :315-317
[19]   Exosomes from Umbilical Cord-Originated Mesenchymal Stem Cells (MSCs) Prevent and Treat Diabetic Nephropathy in Rats via Modulating the Wingless-Related Integration Site (Wnt)/β-Catenin Signal Transduction Pathway [J].
Dong, Fuxing ;
Hong, Fuyuan .
JOURNAL OF BIOMATERIALS AND TISSUE ENGINEERING, 2021, 11 (07) :1305-1312
[20]   Preclinical translation of exosomes derived from mesenchymal stem/stromal cells [J].
Elahi, Fanny M. ;
Farwell, D. Gregory ;
Nolta, Jan A. ;
Anderson, Johnathon D. .
STEM CELLS, 2020, 38 (01) :15-21