Potential applications of mesenchymal stem cells and their derived exosomes in regenerative medicine

被引:23
作者
Adelipour, Maryam [1 ,2 ]
Lubman, David M. [3 ]
Kim, Jeongkwon [1 ]
机构
[1] Chungnam Natl Univ, Dept Chem, Daejeon, South Korea
[2] Ahvaz Jundishapur Univ Med Sci, Dept Biochem, Ahvaz, Iran
[3] Univ Michigan, Dept Surg, Med Ctr, Ann Arbor, MI USA
基金
新加坡国家研究基金会;
关键词
Mesenchymal stem cells; exosomes; extracellular vesicles; regenerative medicine; degenerative disease; BONE-MARROW; EXTRACELLULAR VESICLES; STROMAL CELLS; PARACRINE FUNCTION; OPEN-LABEL; INHIBITION; CONTACT; CULTURE; SAFETY; FLUID;
D O I
10.1080/14712598.2023.2211203
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
IntroductionRegenerative medicine involves the replacement of damaged cells, tissues, or organs to restore normal function. Mesenchymal stem cells (MSCs) and exosomes secreted by MSCs have unique advantages that make them a suitable candidate in the field of regenerative medicine.Areas coveredThis article provides a comprehensive overview of regenerative medicine, focusing on the use of MSCs and their exosomes as potential therapies for replacing damaged cells, tissues, or organs. This article discusses the distinct advantages of both MSCs and their secreted exosomes, including their immunomodulatory effects, lack of immunogenicity, and recruitment to damaged areas. While both MSCs and exosomes have these advantages, MSCs also have the unique ability to self-renew and differentiate. This article also assesses the current challenges associated with the application of MSCs and their secreted exosomes in therapy. We have reviewed proposed solutions for improving MSC or exosome therapy, including ex-vivo preconditioning strategies, genetic modification, and encapsulation. Literature search was conducted using Google Scholar and PubMed databases.Expert opinionProviding insight into the future development of MSC and exosome-based therapies and to encourage the scientific community to focus on the identified gaps, develop appropriate guidelines, and enhance the clinical application of these therapies.
引用
收藏
页码:491 / 507
页数:17
相关论文
共 141 条
[21]   Methods for the identification and characterization of extracellular vesicles in cardiovascular studies: from exosomes to microvesicles [J].
Davidson, Sean M. ;
Boulanger, Chantal M. ;
Aikawa, Elena ;
Badimon, Lina ;
Barile, Lucio ;
Binder, Christoph J. ;
Brisson, Alain ;
Buzas, Edit ;
Emanueli, Costanza ;
Jansen, Felix ;
Katsur, Miroslava ;
Lacroix, Romaric ;
Lim, Sai Kiang ;
Mackman, Nigel ;
Mayr, Manuel ;
Menasche, Philippe ;
Nieuwland, Rienk ;
Sahoo, Susmita ;
Takov, Kaloyan ;
Thum, Thomas ;
Vader, Pieter ;
Wauben, Marca H. M. ;
Witwer, Kenneth ;
Sluijter, Joost P. G. .
CARDIOVASCULAR RESEARCH, 2023, 119 (01) :45-63
[22]   Final Results of Allogeneic Adipose Tissue-Derived Mesenchymal Stem Cells in Acute Ischemic Stroke (AMASCIS): A Phase II, Randomized, Double-Blind, Placebo-Controlled, Single-Center, Pilot Clinical Trial [J].
de Celis-Ruiz, Elena ;
Fuentes, Blanca ;
Alonso de Lecinana, Maria ;
Gutierrez-Fernandez, Maria ;
Borobia, Alberto M. ;
Gutierrez-Zuniga, Raquel ;
Ruiz-Ares, Gerardo ;
Otero-Ortega, Laura ;
Laso-Garcia, Fernando ;
Carmen Gomez-de Frutos, Mari ;
Diez-Tejedor, Exuperio .
CELL TRANSPLANTATION, 2022, 31
[23]   Mesenchymal Stem Cells [J].
Ding, Dah-Ching ;
Shyu, Woei-Cherng ;
Lin, Shinn-Zong .
CELL TRANSPLANTATION, 2011, 20 (01) :5-14
[24]   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
[25]   Bio-instructive hydrogel expands the paracrine potency of mesenchymal stem cells [J].
Drzeniek, Norman M. ;
Mazzocchi, Andrea ;
Schlickeiser, Stephan ;
Forsythe, Steven D. ;
Moll, Guido ;
Geissler, Sven ;
Reinke, Petra ;
Gossen, Manfred ;
Gorantla, Vijay S. ;
Volk, Hans-Dieter ;
Soker, Shay .
BIOFABRICATION, 2021, 13 (04)
[26]   Mesenchymal stem cell inhibition of T-helper 17 cell-differentiation is triggered by cell-cell contact and mediated by prostaglandin E2 via the EP4 receptor [J].
Duffy, Michelle M. ;
Pindjakova, Jana ;
Hanley, Shirley A. ;
McCarthy, Cathal ;
Weidhofer, Gudrun A. ;
Sweeney, Eva M. ;
English, Karen ;
Shaw, Georgina ;
Murphy, J. Mary ;
Barry, Frank P. ;
Mahon, Bernard P. ;
Belton, Orina ;
Ceredig, Rhodri ;
Griffin, Matthew D. .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2011, 41 (10) :2840-2851
[27]   Genetic Modification of Mesenchymal Stem Cells for Neurological Disease Therapy: What Effects Does it Have on Phenotype/Cell Behavior, Determining Their Effectiveness? [J].
Ebrahim, Nour ;
James, Victoria ;
Rizvanov, Albert A. ;
Mukhamedshina, Yana .
MOLECULAR DIAGNOSIS & THERAPY, 2020, 24 (06) :683-702
[28]   Adipose stem cells and their paracrine factors are therapeutic for early retinal complications of diabetes in the Ins2Akita mouse [J].
Elshaer, Sally L. ;
Evans, William ;
Pentecost, Mickey ;
Lenin, Raji ;
Periasamy, Ramesh ;
Jha, Kumar Abhiram ;
Alli, Shanta ;
Gentry, Jordy ;
Thomas, Samuel M. ;
Sohl, Nicolas ;
Gangaraju, Rajashekhar .
STEM CELL RESEARCH & THERAPY, 2018, 9
[29]  
Escacena-Acosta N., 2019, STEM CELLS CONCEPT P, P41
[30]   Dimethyloxalylglycine preconditioning enhances protective effects of bone marrow-derived mesenchymal stem cells in Aβ- induced Alzheimer disease [J].
Esmaeilzade, Banafshe ;
Artimani, Tayebe ;
Amiri, Iraj ;
Najafi, Rezvan ;
Shahidi, Siamak ;
Sabec, Marie ;
Farzadinia, Parviz ;
Zare, Mohammadali ;
Zahiri, Maria ;
Asl, Sara Soleimani .
PHYSIOLOGY & BEHAVIOR, 2019, 199 :265-272