Mesenchymal Stromal Cell-Derived Extracellular Vesicles - Silver Linings for Cartilage Regeneration?

被引:13
作者
De Luna, Andrea [1 ]
Otahal, Alexander [1 ]
Nehrer, Stefan [1 ]
机构
[1] Danube Univ Krems, Dept Hlth Sci Med & Res, Ctr Regenerat Med, Krems An Der Donau, Austria
关键词
mesenchymal stem cell; extracellular vesicle; osteoarthritis; biomarkers; in vitro studies and in vivo studies; PI3K/AKT SIGNALING PATHWAY; STEM-CELLS; KNEE OSTEOARTHRITIS; CHONDROGENIC DIFFERENTIATION; UP-REGULATION; SYNOVIAL-FLUID; EXOSOMES; MICRORNA; TISSUE; THERAPY;
D O I
10.3389/fcell.2020.593386
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
As the world's population is aging, the incidence of the degenerative disease Osteoarthritis (OA) is increasing. Current treatment options of OA focus on the alleviation of the symptoms including pain and inflammation rather than on restoration of the articular cartilage. Cell-based therapies including the application of mesenchymal stromal cells (MSCs) have been a promising tool for cartilage regeneration approaches. Due to their immunomodulatory properties, their differentiation potential into cells of the mesodermal lineage as well as the plurality of sources from which they can be isolated, MSCs have been applied in a vast number of studies focusing on the establishment of new treatment options for Osteoarthritis. Despite promising outcomes in vitro and in vivo, applications of MSCs are connected with teratoma formation, limited lifespan of differentiated cells as well as rejection of the cells after transplantation, highlighting the need for new cell free approaches harboring the beneficial properties of MSCs. It has been demonstrated that the regenerative potential of MSCs is mediated by the release of paracrine factors rather than by differentiation into cells of the desired tissue. Besides soluble factors, extracellular vesicles are the major component of a cell's secretome. They represent novel mechanisms by which (pathogenic) signals can be communicated between cell types as they deliver bioactive molecules (nucleic acids, proteins, lipids) from the cell of origin to the target cell leading to specific biological processes upon uptake. This review will give an overview about extracellular vesicles including general characteristics, isolation methods and characterization approaches. Furthermore, the role of MSC-derived extracellular vesicles in in vitro and in vivo studies for cartilage regeneration will be summarized with special focus on transported miRNA which either favored the progression of OA or protected the cartilage from degradation. In addition, studies will be reviewed investigating the impact of MSC-derived extracellular vesicles on inflammatory arthritis. As extracellular vesicles are present in all body fluids, their application as potential biomarkers for OA will also be discussed in this review. Finally, studies exploring the combination of MSC-derived extracellular vesicles with biomaterials for tissue engineering approaches are summarized.
引用
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页数:16
相关论文
共 153 条
[81]
Exosomes and Ectosomes in Intercellular Communication [J].
Meldolesi, Jacopo .
CURRENT BIOLOGY, 2018, 28 (08) :R435-R444
[82]
Cancer-Derived Extracellular Vesicle-Associated MicroRNAs in Intercellular Communication: One Cell's Trash Is Another Cell's Treasure [J].
Mills, Joseph ;
Capece, Marina ;
Cocucci, Emanuele ;
Tessari, Anna ;
Palmieri, Dario .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2019, 20 (24)
[83]
MicroRNA-140 plays dual roles in both cartilage development and homeostasis [J].
Miyaki, Shigeru ;
Sato, Tempei ;
Inoue, Atsushi ;
Otsuki, Shuhei ;
Ito, Yoshiaki ;
Yokoyama, Shigetoshi ;
Kato, Yoshio ;
Takemoto, Fuko ;
Nakasa, Tomoyuki ;
Yamashita, Satoshi ;
Takada, Shuji ;
Lotz, Martin K. ;
Ueno-Kudo, Hiroe ;
Asahara, Hiroshi .
GENES & DEVELOPMENT, 2010, 24 (11) :1173-1185
[84]
MicroRNA-140 Is Expressed in Differentiated Human Articular Chondrocytes and Modulates Interleukin-1 Responses [J].
Miyaki, Shigeru ;
Nakasa, Tomoyuki ;
Otsuki, Shuhei ;
Grogan, Shawn P. ;
Higashiyama, Reiji ;
Inoue, Atsushi ;
Kato, Yoshio ;
Sato, Tempei ;
Lotz, Martin K. ;
Asahara, Hiroshi .
ARTHRITIS AND RHEUMATISM, 2009, 60 (09) :2723-2730
[85]
Plasma and synovial fluid microRNAs as potential biomarkers of rheumatoid arthritis and osteoarthritis [J].
Murata, Koichi ;
Yoshitomi, Hiroyuki ;
Tanida, Shimei ;
Ishikawa, Masahiro ;
Nishitani, Kohei ;
Ito, Hiromu ;
Nakamura, Takashi .
ARTHRITIS RESEARCH & THERAPY, 2010, 12 (03)
[86]
Emerging role of extracellular vesicles in musculoskeletal diseases [J].
Murphy, Cameron ;
Withrow, Joseph ;
Hunter, Monte ;
Liu, Yutao ;
Tang, Yao Liang ;
Fulzele, Sadanand ;
Hamrick, Mark W. .
MOLECULAR ASPECTS OF MEDICINE, 2018, 60 :123-128
[87]
Mesenchymal stem cells: environmentally responsive therapeutics for regenerative medicine [J].
Murphy, Matthew B. ;
Moncivais, Kathryn ;
Caplan, Arnold I. .
EXPERIMENTAL AND MOLECULAR MEDICINE, 2013, 45 :e54-e54
[88]
Exosomes: roles and therapeutic potential in osteoarthritis [J].
Ni, Zhenhong ;
Zhou, Siru ;
Li, Song ;
Kuang, Liang ;
Chen, Hangang ;
Luo, Xiaoqing ;
Ouyang, Junjie ;
He, Mei ;
Du, Xiaolan ;
Chen, Lin .
BONE RESEARCH, 2020, 8 (01)
[89]
The exosome-like vesicles from osteoarthritic chondrocyte enhanced mature IL-1β production of macrophages and aggravated synovitis in osteoarthritis [J].
Ni, Zhenhong ;
Kuang, Liang ;
Chen, Hangang ;
Xie, Yangli ;
Zhang, Bin ;
Ouyang, Junjie ;
Wu, Jiangyi ;
Zhou, Siru ;
Chen, Liang ;
Su, Nan ;
Tan, QiaoYan ;
Luo, Xiaoqing ;
Chen, Bo ;
Chen, Shuai ;
Yin, Liangjun ;
Huang, Haiyang ;
Du, Xiaolan ;
Chen, Lin .
CELL DEATH & DISEASE, 2019, 10 (7)
[90]
MicroRNA-92a Upholds Bmp Signaling by Targeting noggin3 during Pharyngeal Cartilage Formation [J].
Ning, Guozhu ;
Liu, Xiuli ;
Dai, Miaomiao ;
Meng, Anming ;
Wang, Qiang .
DEVELOPMENTAL CELL, 2013, 24 (03) :283-295