Mesenchymal stem cell derived-exosomes: a modern approach in translational medicine

被引:316
作者
Nikfarjam, Sepideh [1 ]
Rezaie, Jafar [2 ]
Zolbanin, Naime Majidi [3 ]
Jafari, Reza [2 ]
机构
[1] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Biotechnol, Tabriz, Iran
[2] Urmia Univ Med Sci, Cellular & Mol Med Res Inst, Solid Tumor Res Ctr, Shafa St,Ershad Blvd,POB 1138, Orumiyeh 57147, Iran
[3] Urmia Univ Med Sci, Fac Pharm, Dept Pharmacol & Toxicol, Orumiyeh, Iran
关键词
Mesenchymal stem cell; Exosome; Extracellular vesicle; Exosome isolation; Regenerative medicine; EXTRACELLULAR VESICLES PROTECT; STROMAL CELLS; FUNCTIONAL RECOVERY; NEUROVASCULAR PLASTICITY; INFLAMMATORY RESPONSES; MYOCARDIAL-INFARCTION; ENHANCE ANGIOGENESIS; CARDIAC-FUNCTION; IMPROVE; KIDNEY;
D O I
10.1186/s12967-020-02622-3
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Mesenchymal stem cells (MSCs) have captured great attention in regenerative medicine for over a few decades by virtue of their differentiation capacity, potent immunomodulatory properties, and their ability to be favorably cultured and manipulated. Recent investigations implied that the pleiotropic effects of MSCs is not associated to their ability of differentiation, but rather is mediated by the secretion of soluble paracrine factors. Exosomes, nanoscale extracellular vesicles, are one of these paracrine mediators. Exosomes transfer functional cargos like miRNA and mRNA molecules, peptides, proteins, cytokines and lipids from MSCs to the recipient cells. Exosomes participate in intercellular communication events and contribute to the healing of injured or diseased tissues and organs. Studies reported that exosomes alone are responsible for the therapeutic effects of MSCs in numerous experimental models. Therefore, MSC-derived exosomes can be manipulated and applied to establish a novel cell-free therapeutic approach for treatment of a variety of diseases including heart, kidney, liver, immune and neurological diseases, and cutaneous wound healing. In comparison with their donor cells, MSC-derived exosomes offer more stable entities and diminished safety risks regarding the administration of live cells, e.g. microvasculature occlusion risk. This review discusses the exosome isolation methods invented and utilized in the clinical setting thus far and presents a summary of current information on MSC exosomes in translational medicine.
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页数:21
相关论文
共 120 条
[1]   Proteomic analysis of exosomal cargo: the challenge of high purity vesicle isolation [J].
Abramowicz, Agata ;
Widlak, Piotr ;
Pietrowska, Monika .
MOLECULAR BIOSYSTEMS, 2016, 12 (05) :1407-1419
[2]   Free and hydrogel encapsulated exosome-based therapies in regenerative medicine [J].
Akbari, Ali ;
Jabbari, Nassrollah ;
Sharifi, Roholah ;
Ahmadi, Mahdi ;
Vahhabi, Ali ;
Seyedzadeh, Seyyed Javad ;
Nawaz, Muhammad ;
Szafert, Slawomir ;
Mahmoodi, Monireh ;
Jabbari, Esmaiel ;
Asghari, Rahim ;
Rezaie, Jafar .
LIFE SCIENCES, 2020, 249
[3]   Exosomes From Human Cardiac Progenitor Cells for Therapeutic Applications: Development of a GMP-Grade Manufacturing Method [J].
Andriolo, Gabriella ;
Provasi, Elena ;
Lo Cicero, Viviana ;
Brambilla, Andrea ;
Soncin, Sabrina ;
Torre, Tiziano ;
Milano, Giuseppina ;
Biemmi, Vanessa ;
Vassalli, Giuseppe ;
Turchetto, Lucia ;
Barile, Lucio ;
Radrizzani, Marina .
FRONTIERS IN PHYSIOLOGY, 2018, 9
[4]   Dendritic cell-derived exosomes as maintenance immunotherapy after first line chemotherapy in NSCLC [J].
Besse, Benjamin ;
Charrier, Melinda ;
Lapierre, Valerie ;
Dansin, Eric ;
Lantz, Olivier ;
Planchard, David ;
Le Chevalier, Thierry ;
Livartoski, Alain ;
Barlesik, Fabrice ;
Laplanche, Agnes ;
Ploix, Stephanie ;
Vimond, Nadege ;
Peguillet, Isabelle ;
Thery, Clotilde ;
Lacroix, Ludovic ;
Zoernig, Inka ;
Dhodapkar, Kavita ;
Dhodapkar, Madhav ;
Viaud, Sophie ;
Soria, Jean-Charles ;
Reiners, Katrin S. ;
von Strandmann, Elke Pogge ;
Vely, Frederic ;
Rusakiewicz, Sylvie ;
Eggermont, Alexander ;
Pitt, Jonathan M. ;
Zitvogel, Laurence ;
Chaput, Nathalie .
ONCOIMMUNOLOGY, 2016, 5 (04)
[5]   Extracellular vesicles derived from human bone marrow mesenchymal stem cells promote angiogenesis in a rat myocardial infarction model [J].
Bian, Suyan ;
Zhang, Liping ;
Duan, Liufa ;
Wang, Xi ;
Min, Ying ;
Yu, Hepeng .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2014, 92 (04) :387-397
[6]   Mesenchymal Stem/Stromal Cell-Derived Extracellular Vesicles and Their Potential as Novel Immunomodulatory Therapeutic Agents [J].
Boerger, Verena ;
Bremer, Michel ;
Ferrer-Tur, Rita ;
Gockeln, Lena ;
Stambouli, Oumaima ;
Becic, Amina ;
Giebel, Bernd .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2017, 18 (07)
[7]  
Bruno S, 2017, TISSUE ENG PT A, V23, P1262, DOI [10.1089/ten.tea.2017.0069, 10.1089/ten.TEA.2017.0069]
[8]   Tangential Flow Filtration for Highly Efficient Concentration of Extracellular Vesicles from Large Volumes of Fluid [J].
Busatto, Sara ;
Vilanilam, George ;
Ticer, Taylor ;
Lin, Wen-Lang ;
Dickson, Dennis W. ;
Shapiro, Shane ;
Bergese, Paolo ;
Wolfram, Joy .
CELLS, 2018, 7 (12)
[9]   Exosomes derived from GDNF-modified human adipose mesenchymal stem cells ameliorate peritubular capillary loss in tubulointerstitial fibrosis by activating the SIRT1/eNOS signaling pathway [J].
Chen, Lu ;
Wang, Yanping ;
Li, Shulin ;
Zuo, Bangjie ;
Zhang, Xiangyu ;
Wang, Fengzhen ;
Sun, Dong .
THERANOSTICS, 2020, 10 (20) :9425-9442
[10]   Different populations of Wnt-containing vesicles are individually released from polarized epithelial cells [J].
Chen, Qiuhong ;
Takada, Ritsuko ;
Noda, Chiyo ;
Kobayashi, Satoru ;
Takada, Shinji .
SCIENTIFIC REPORTS, 2016, 6