Mesenchymal Stem Cell-Derived Extracellular Vesicles to the Rescue of Renal Injury

被引:70
作者
Birtwistle, Lucy [1 ]
Chen, Xin-Ming [2 ]
Pollock, Carol [2 ]
机构
[1] Univ Sydney, Fac Med & Hlth, Sydney Med Sch, Camperdown, NSW 2050, Australia
[2] Univ Sydney, Royal North Shore Hosp, Sydney Med Sch, Kolling Inst, St Leonards, NSW 2065, Australia
关键词
extracellular vesicle; exosome; mesenchymal stem cells; acute kidney injury; chronic kidney disease; miRNA; CHRONIC KIDNEY-DISEASE; ISCHEMIA-REPERFUSION INJURY; HUMAN UMBILICAL-CORD; PERITUBULAR CAPILLARY RAREFACTION; STROMAL CELLS; DIABETIC-NEPHROPATHY; TUBULOINTERSTITIAL FIBROSIS; METABOLIC SYNDROME; IN-VIVO; MICROVESICLES PROTECT;
D O I
10.3390/ijms22126596
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
Acute kidney injury (AKI) and chronic kidney disease (CKD) are rising in global prevalence and cause significant morbidity for patients. Current treatments are limited to slowing instead of stabilising or reversing disease progression. In this review, we describe mesenchymal stem cells (MSCs) and their constituents, extracellular vesicles (EVs) as being a novel therapeutic for CKD. MSC-derived EVs (MSC-EVs) are membrane-enclosed particles, including exosomes, which carry genetic information that mimics the phenotype of their cell of origin. MSC-EVs deliver their cargo of mRNA, miRNA, cytokines, and growth factors to target cells as a form of paracrine communication. This genetically reprograms pathophysiological pathways, which are upregulated in renal failure. Since the method of exosome preparation significantly affects the quality and function of MSC-exosomes, this review compares the methodologies for isolating exosomes from MSCs and their role in tissue regeneration. More specifically, it summarises the therapeutic efficacy of MSC-EVs in 60 preclinical animal models of AKI and CKD and the cargo of biomolecules they deliver. MSC-EVs promote tubular proliferation and angiogenesis, and inhibit apoptosis, oxidative stress, inflammation, the epithelial-to-mesenchymal transition, and fibrosis, to alleviate AKI and CKD. By reprogramming these pathophysiological pathways, MSC-EVs can slow or even reverse the progression of AKI to CKD, and therefore offer potential to transform clinical practice.
引用
收藏
页数:27
相关论文
共 189 条
[1]   Comprehensive review on lactate metabolism in human health [J].
Adeva-Andany, M. ;
Lopez-Ojen, M. ;
Funcasta-Calderon, R. ;
Ameneiros-Rodriguez, E. ;
Donapetry-Garcia, C. ;
Vila-Altesor, M. ;
Rodriguez-Seijas, J. .
MITOCHONDRION, 2014, 17 :76-100
[2]   Biogenesis of extracellular vesicles (EV): exosomes, microvesicles, retrovirus-like vesicles, and apoptotic bodies [J].
Akers, Johnny C. ;
Gonda, David ;
Kim, Ryan ;
Carter, Bob S. ;
Chen, Clark C. .
JOURNAL OF NEURO-ONCOLOGY, 2013, 113 (01) :1-11
[3]   Delivery of siRNA to the mouse brain by systemic injection of targeted exosomes [J].
Alvarez-Erviti, Lydia ;
Seow, Yiqi ;
Yin, HaiFang ;
Betts, Corinne ;
Lakhal, Samira ;
Wood, Matthew J. A. .
NATURE BIOTECHNOLOGY, 2011, 29 (04) :341-U179
[4]  
Alzahrani FA, 2019, AM J TRANSL RES, V11, P2887
[5]  
ANZDATA Registry, 2017, 40 ANN ANZ REP AUSTR
[6]  
Australian Institute of Health and Welfare, 2019, CHR KIDN DIS
[7]  
Australian Institute of Health and Welfare, 2018, ADM PAT CAR 2014 15
[8]   Short ischemia induces rat kidney mitochondria dysfunction [J].
Baniene, Rasa ;
Trumbeckas, Darius ;
Kincius, Marius ;
Pauziene, Neringa ;
Raudone, Lina ;
Jievaltas, Mindaugas ;
Trumbeckaite, Sonata .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2016, 48 (01) :77-85
[9]   Safety and Efficacy Endpoints for Mesenchymal Stromal Cell Therapy in Renal Transplant Recipients [J].
Bank, J. R. ;
Rabelink, T. J. ;
de Fijter, J. W. ;
Reinders, M. E. J. .
JOURNAL OF IMMUNOLOGY RESEARCH, 2015, 2015
[10]   Assessment of Global Kidney Health Care Status [J].
Bello, Aminu K. ;
Levin, Adeera ;
Tonelli, Marcello ;
Okpechi, Ikechi G. ;
Feehally, John ;
Harris, David ;
Jindal, Kailash ;
Salako, Babatunde L. ;
Rateb, Ahmed ;
Osman, Mohamed A. ;
Qarni, Bilal ;
Saad, Syed ;
Lunney, Meaghan ;
Wiebe, Natasha ;
Johnson, David W. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2017, 317 (18) :1864-1881