iPSCs in Modeling and Therapy of Osteoarthritis

被引:25
作者
Csobonyeiova, Maria [1 ]
Polak, Stefan [1 ]
Nicodemou, Andreas [2 ]
Zamborsky, Radoslav [3 ]
Danisovic, Lubos [2 ,4 ]
机构
[1] Comenius Univ, Inst Histol & Embryol, Fac Med, Sasinkova 4, Bratislava 81108, Slovakia
[2] Comenius Univ, Fac Med, Inst Med Biol Genet & Clin Genet, Sasinkova 4, Bratislava 81108, Slovakia
[3] Comenius Univ, Fac Med, Dept Orthoped, Natl Inst Childrens Dis, Limbova 1, Bratislava 83340, Slovakia
[4] Regenmed Ltd, Medena 29, Bratislava 81101, Slovakia
关键词
osteoarthritis; iPSCs; articular cartilage; stem cell-based therapy; disease modeling; PLURIPOTENT STEM-CELLS; CHONDROGENIC DIFFERENTIATION; DIRECTED DIFFERENTIATION; CARTILAGE; GENERATION; TISSUE; INDUCTION; CHONDROCYTES; FIBROBLASTS; MOUSE;
D O I
10.3390/biomedicines9020186
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
Osteoarthritis (OA) belongs to chronic degenerative disorders and is often a leading cause of disability in elderly patients. Typically, OA is manifested by articular cartilage erosion, pain, stiffness, and crepitus. Currently, the treatment options are limited, relying mostly on pharmacological therapy, which is often related to numerous complications. The proper management of the disease is challenging because of the poor regenerative capacity of articular cartilage. During the last decade, cell-based approaches such as implantation of autologous chondrocytes or mesenchymal stem cells (MSCs) have shown promising results. However, the mentioned techniques face their hurdles (cell harvesting, low proliferation capacity). The invention of induced pluripotent stem cells (iPSCs) has created new opportunities to increase the efficacy of the cartilage healing process. iPSCs may represent an unlimited source of chondrocytes derived from a patient's somatic cells, circumventing ethical and immunological issues. Aside from the regenerative potential of iPSCs, stem cell-derived cartilage tissue models could be a useful tool for studying the pathological process of OA. In our recent article, we reviewed the progress in chondrocyte differentiation techniques, disease modeling, and the current status of iPSC-based regenerative therapy of OA.
引用
收藏
页码:1 / 12
页数:12
相关论文
共 50 条
[1]  
[Anonymous], 2014, THE J, DOI DOI 10.1055/s-0034-1390329
[2]   Selected small molecules as inducers of pluripotency [J].
Baranek, Malgorzata ;
Markiewicz, Wojciech T. ;
Barciszewski, Jan .
ACTA BIOCHIMICA POLONICA, 2016, 63 (04) :709-716
[3]  
Cheng AX, 2014, TISSUE ENG PART B-RE, V20, P257, DOI [10.1089/ten.teb.2012.0757, 10.1089/ten.TEB.2012.0757]
[4]  
Chu CR, 2010, TISSUE ENG PART B-RE, V16, P105, DOI [10.1089/ten.teb.2009.0452, 10.1089/ten.TEB.2009.0452]
[5]   Induction of pluripotency in long-term cryopreserved human neonatal fibroblasts in feeder-free condition [J].
Csobonyeiova, Maria ;
Krajciova, Lubica ;
Nicodemou, Andreas ;
Polak, Stefan ;
Danisovic, Lubos .
CELL AND TISSUE BANKING, 2017, 18 (01) :45-52
[6]   Cartilage tissue engineering using differentiated and purified induced pluripotent stem cells [J].
Diekman, Brian O. ;
Christoforou, Nicolas ;
Willard, Vincent P. ;
Sun, Haosi ;
Sanchez-Adams, Johannah ;
Leong, Kam W. ;
Guilak, Farshid .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2012, 109 (47) :19172-19177
[7]   Cellular reprogramming for clinical cartilage repair [J].
Driessen, Britta J. H. ;
Logie, Colin ;
Vonk, Lucienne A. .
CELL BIOLOGY AND TOXICOLOGY, 2017, 33 (04) :329-349
[8]   Combating Osteoarthritis through Stem Cell Therapies by Rejuvenating Cartilage: A Review [J].
Dubey, Navneet Kumar ;
Mishra, Viraj Krishna ;
Dubey, Rajni ;
Syed-Abdul, Shabbir ;
Wang, Joseph R. ;
Wang, Peter D. ;
Deng, Win-Ping .
STEM CELLS INTERNATIONAL, 2018, 2018
[9]  
Fukunaga N, 2010, CELL REPROGRAM, V12, P369, DOI [10.1089/cell.2009.0097, 10.1089/cell.2009.0086]
[10]   Efficient induction of transgene-free human pluripotent stem cells using a vector based on Sendai virus, an RNA virus that does not integrate into the host genome [J].
Fusaki, Noemi ;
Ban, Hiroshi ;
Nishiyama, Akiyo ;
Saeki, Koichi ;
Hasegawa, Mamoru .
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES, 2009, 85 (08) :348-362