iPSC Therapy for Myocardial Infarction in Large Animal Models: Land of Hope and Dreams

被引:13
作者
Martinez-Falguera, Daina [1 ,2 ,3 ]
Iborra-Egea, Oriol [2 ,3 ]
Galvez-Monton, Carolina [2 ,3 ,4 ,5 ]
机构
[1] Univ Barcelona UB, Fac Med, Barcelona 08036, Spain
[2] Germans Trias & Pujol Hlth Res Inst, ICREC Res Program, Can Ruti Campus, Badalona 08916, Spain
[3] Germans Trias & Pujol Univ Hosp, Heart Inst iCor, Badalona 08916, Spain
[4] Inst Salud Carlos III, CIBERCV, Madrid 28029, Spain
[5] Inst Invest Biomed Bellvitge IDIBELL, Barcelona 08908, Spain
关键词
induced pluripotent stem cells; cardiovascular disease; myocardial infarction; large animal models; cardiac regeneration; PLURIPOTENT STEM-CELLS; MAJOR HISTOCOMPATIBILITY COMPLEX; LEUKEMIA INHIBITORY FACTOR; ENGINEERED CARDIAC PATCH; HEART-FAILURE; FUNCTIONAL CONSEQUENCES; HIGH-RESOLUTION; PORCINE MODEL; SENDAI-VIRUS; SWINE MODEL;
D O I
10.3390/biomedicines9121836
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
Myocardial infarction is the main driver of heart failure due to ischemia and subsequent cell death, and cell-based strategies have emerged as promising therapeutic methods to replace dead tissue in cardiovascular diseases. Research in this field has been dramatically advanced by the development of laboratory-induced pluripotent stem cells (iPSCs) that harbor the capability to become any cell type. Like other experimental strategies, stem cell therapy must meet multiple requirements before reaching the clinical trial phase, and in vivo models are indispensable for ensuring the safety of such novel therapies. Specifically, translational studies in large animal models are necessary to fully evaluate the therapeutic potential of this approach; to empirically determine the optimal combination of cell types, supplementary factors, and delivery methods to maximize efficacy; and to stringently assess safety. In the present review, we summarize the main strategies employed to generate iPSCs and differentiate them into cardiomyocytes in large animal species; the most critical differences between using small versus large animal models for cardiovascular studies; and the strategies that have been pursued regarding implanted cells' stage of differentiation, origin, and technical application.
引用
收藏
页数:25
相关论文
共 222 条
[21]  
Burridge PW, 2014, NAT METHODS, V11, P855, DOI [10.1038/NMETH.2999, 10.1038/nmeth.2999]
[22]   A Universal System for Highly Efficient Cardiac Differentiation of Human Induced Pluripotent Stem Cells That Eliminates Interline Variability [J].
Burridge, Paul W. ;
Thompson, Susan ;
Millrod, Michal A. ;
Weinberg, Seth ;
Yuan, Xuan ;
Peters, Ann ;
Mahairaki, Vasiliki ;
Koliatsos, Vassilis E. ;
Tung, Leslie ;
Zambidis, Elias T. .
PLOS ONE, 2011, 6 (04)
[23]   Characterization of Bovine Induced Pluripotent Stem Cells by Lentiviral Transduction of Reprogramming Factor Fusion Proteins [J].
Cao, Hongguo ;
Yang, Pan ;
Pu, Yong ;
Sun, Xueping ;
Yin, Huiqun ;
Zhang, Yu ;
Zhang, Yunhai ;
Li, Yunsheng ;
Liu, Ya ;
Fang, Fugui ;
Zhang, Zijun ;
Tao, Yong ;
Zhang, Xiaorong .
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2012, 8 (04) :498-511
[24]   Ascorbic acid enhances the cardiac differentiation of induced pluripotent stem cells through promoting the proliferation of cardiac progenitor cells [J].
Cao, Nan ;
Liu, Zumei ;
Chen, Zhongyan ;
Wang, Jia ;
Chen, Taotao ;
Zhao, Xiaoyang ;
Ma, Yu ;
Qin, Lianju ;
Kang, Jiuhong ;
Wei, Bin ;
Wang, Liu ;
Jin, Ying ;
Yang, Huang-Tian .
CELL RESEARCH, 2012, 22 (01) :219-236
[25]   Generation of a pig induced pluripotent stem cell (piPSC) line from embryonic fibroblasts by incorporating LIN28 to the four transcriptional factor-mediated reprogramming: VSMUi001-D [J].
Chakritbudsabong, Warunya ;
Sariya, Ladawan ;
Pamonsupornvichit, Sirikron ;
Pronarkngver, Rassmeepen ;
Chaiwattanarungruengpaisan, Somjit ;
Ferreira, Joao N. ;
Setthawong, Piyathip ;
Phakdeedindan, Praopilas ;
Techakumphu, Mongkol ;
Tharasanit, Theerawat ;
Rungarunlert, Sasitorn .
STEM CELL RESEARCH, 2017, 24 :21-24
[26]   The Anti-Inflammatory and Antibacterial Basis of Human Omental Defense: Selective Expression of Cytokines and Antimicrobial Peptides [J].
Chandra, Abhijit ;
Srivastava, Ritesh Kumar ;
Kashyap, Mahendra Pratap ;
Kumar, Raj ;
Srivastava, Rajeshwar Nath ;
Pant, Aditya Bhushan .
PLOS ONE, 2011, 6 (05)
[27]   Inducing goat pluripotent stem cells with four transcription factor mRNAs that activate endogenous promoters [J].
Chen, Hao ;
Zuo, Qisheng ;
Wang, Yingjie ;
Song, Jiuzhou ;
Yang, Huilin ;
Zhang, Yani ;
Li, Bichun .
BMC BIOTECHNOLOGY, 2017, 17
[28]   Porcine Induced Pluripotent Stem Cells Require LIF and Maintain Their Developmental Potential in Early Stage of Embryos [J].
Cheng, De ;
Guo, Yanjie ;
Li, Zhenzhen ;
Liu, Yajun ;
Gao, Xing ;
Gao, Yi ;
Cheng, Xiang ;
Hu, Junhe ;
Wang, Huayan .
PLOS ONE, 2012, 7 (12)
[29]   Methods of Generation of Induced Pluripotent Stem Cells and Their Application for the Therapy of Central Nervous System Diseases [J].
Cherkashova, E. A. ;
Leonov, G. E. ;
Namestnikova, D. D. ;
Solov'eva, A. A. ;
Gubskii, I. L. ;
Bukharova, T. B. ;
Gubskii, L. V. ;
Goldstein, D. V. ;
Yarygin, K. N. .
BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE, 2020, 168 (04) :566-573
[30]   Differentiation of equine induced pluripotent stem cells into mesenchymal lineage for therapeutic use [J].
Chung, Myung-Jin ;
Park, SunYoung ;
Son, Ji-Yoon ;
Lee, Jae-Yeong ;
Yun, Hyun Ho ;
Lee, Eun-Joo ;
Lee, Eun Mi ;
Cho, Gil-Jae ;
Lee, Sunray ;
Park, Hyun-Sook ;
Jeong, Kyu-Shik .
CELL CYCLE, 2019, 18 (21) :2954-2971