Genetic cell reprogramming: A new technology for basic research and applied usage

被引:8
作者
Bogomazova, A. N. [1 ,2 ]
Vassina, E. M. [1 ,2 ]
Kiselev, S. L. [1 ,2 ]
Lagarkova, M. A. [1 ,2 ]
Lebedeva, O. S. [1 ]
Nekrasov, E. D. [1 ,2 ]
Panova, A. V. [1 ,2 ]
Philonenko, E. S. [1 ,2 ]
Khomyakova, E. A. [1 ,2 ]
Tskhovrebova, L. V. [1 ]
Chestkov, I. V. [1 ,2 ]
Shutova, M. V. [1 ,2 ]
机构
[1] Russian Acad Sci, Vavilov Inst Gen Genet, Moscow 119991, Russia
[2] Scoltech Ctr Stem Cell Res, Moscow 143026, Russia
基金
俄罗斯基础研究基金会;
关键词
PLURIPOTENT STEM-CELLS; RETINAL-PIGMENT EPITHELIUM; ALZHEIMERS-DISEASE; SENDAI-VIRUS; GENERATION; LINES; DIFFERENTIATION; FIBROBLASTS; EXPRESSION; INDUCTION;
D O I
10.1134/S102279541504002X
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Gene function disclosure and the development of modern technologies of genetic manipulations offered the possibility of genetic reprogramming application to alter cell specialization. With the involvement of a gene set that encodes the transcription factors responsible for the pluripotent state, any cell of an adult body could be reprogrammed into the embryonal state and pluripotency could be induced in this cell. Such reprogrammed cells were called induced pluripotent stem cells (iPSCs), and they are capable of again passing through all developmental stages. This provides new possibilities for studies of the basic mechanisms of developmental biology, the formation of specific cell types, and the whole body. In culture, iPSCs could be maintained permanently in a nontransformed state and permit genetic manipulations while maintaining their pluripotent properties. Such a unique combination of their properties makes them an attractive tool for studies of various pathologies and for the delineation of treatment approaches. This review discusses the basic and applied aspects of iPSCs biology.
引用
收藏
页码:386 / 396
页数:11
相关论文
共 68 条
[1]   Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage [J].
Amps, Katherine ;
Andrews, Peter W. ;
Anyfantis, George ;
Armstrong, Lyle ;
Avery, Stuart ;
Baharvand, Hossein ;
Baker, Julie ;
Baker, Duncan ;
Munoz, Maria B. ;
Beil, Stephen ;
Benvenisty, Nissim ;
Ben-Yosef, Dalit ;
Biancotti, Juan-Carlos ;
Bosman, Alexis ;
Brena, Romulo Martin ;
Brison, Daniel ;
Caisander, Gunilla ;
Camarasa, Maria V. ;
Chen, Jieming ;
Chiao, Eric ;
Choi, Young Min ;
Choo, Andre B. H. ;
Collins, Daniel ;
Colman, Alan ;
Crook, Jeremy M. ;
Daley, George Q. ;
Dalton, Anne ;
De Sousa, Paul A. ;
Denning, Chris ;
Downie, Janet ;
Dvorak, Petr ;
Montgomery, Karen D. ;
Feki, Anis ;
Ford, Angela ;
Fox, Victoria ;
Fraga, Ana M. ;
Frumkin, Tzvia ;
Ge, Lin ;
Gokhale, Paul J. ;
Golan-Lev, Tamar ;
Gourabi, Hamid ;
Gropp, Michal ;
Lu Guangxiu ;
Hampl, Ales ;
Harron, Katie ;
Healy, Lyn ;
Herath, Wishva ;
Holm, Frida ;
Hovatta, Outi ;
Hyllner, Johan .
NATURE BIOTECHNOLOGY, 2011, 29 (12) :1132-U113
[2]   Innate Immune Suppression Enables Frequent Transfection with RNA Encoding Reprogramming Proteins [J].
Angel, Matthew ;
Yanik, Mehmet Fatih .
PLOS ONE, 2010, 5 (07)
[3]   Senescence impairs successful reprogramming to pluripotent stem cells [J].
Banito, Ana ;
Rashid, Sheikh T. ;
Acosta, Juan Carlos ;
Li, SiDe ;
Pereira, Carlos F. ;
Geti, Imbisaat ;
Pinho, Sandra ;
Silva, Jose C. ;
Azuara, Veronique ;
Walsh, Martin ;
Vallier, Ludovic ;
Gil, Jesus .
GENES & DEVELOPMENT, 2009, 23 (18) :2134-2139
[4]   Cell-autonomous correction of ring chromosomes in human induced pluripotent stem cells [J].
Bershteyn, Marina ;
Hayashi, Yohei ;
Desachy, Guillaume ;
Hsiao, Edward C. ;
Sami, Salma ;
Tsang, Kathryn M. ;
Weiss, Lauren A. ;
Kriegstein, Arnold R. ;
Yamanaka, Shinya ;
Wynshaw-Boris, Anthony .
NATURE, 2014, 507 (7490) :99-+
[5]   Reference Maps of Human ES and iPS Cell Variation Enable High-Throughput Characterization of Pluripotent Cell Lines [J].
Bock, Christoph ;
Kiskinis, Evangelos ;
Verstappen, Griet ;
Gu, Hongcang ;
Boulting, Gabriella ;
Smith, Zachary D. ;
Ziller, Michael ;
Croft, Gist F. ;
Amoroso, Mackenzie W. ;
Oakley, Derek H. ;
Gnirke, Andreas ;
Eggan, Kevin ;
Meissner, Alexander .
CELL, 2011, 144 (03) :439-452
[6]   Reactivation of Dyen chromosome upon reprogramming leads to changes in the replication pattern and 5hmC accumulation [J].
Bogomazova, Alexandra N. ;
Lagarkova, Maria A. ;
Panova, Alexandra V. ;
Nekrasov, Evgueny D. ;
Kiselev, Sergey L. .
CHROMOSOMA, 2014, 123 (1-2) :117-128
[7]   Modelling schizophrenia using human induced pluripotent stem cells [J].
Brennand, Kristen J. ;
Simone, Anthony ;
Jou, Jessica ;
Gelboin-Burkhart, Chelsea ;
Tran, Ngoc ;
Sangar, Sarah ;
Li, Yan ;
Mu, Yangling ;
Chen, Gong ;
Yu, Diana ;
McCarthy, Shane ;
Sebat, Jonathan ;
Gage, Fred H. .
NATURE, 2011, 473 (7346) :221-+
[8]   Meta-analysis of the heterogeneity of X chromosome inactivation in human pluripotent stem cells [J].
Bruck, Tal ;
Benvenisty, Nissim .
STEM CELL RESEARCH, 2011, 6 (02) :187-193
[9]  
Chang C.J., 2011, PLOS ONE
[10]   Patient-Specific Induced Pluripotent Stem Cells for SOD1-Associated Amyotrophic Lateral Sclerosis Pathogenesis Studies [J].
Chestkov, I. V. ;
Vasilieva, E. A. ;
Illarioshkin, S. N. ;
Lagarkova, M. A. ;
Kiselev, S. L. .
ACTA NATURAE, 2014, 6 (01) :54-60