scholarly journals Cellular Ontogeny and Hierarchy Influence the Reprogramming Efficiency of Human B Cells into Induced Pluripotent Stem Cells

Stem Cells ◽  
2016 ◽  
Vol 34 (3) ◽  
pp. 581-587 ◽  
Author(s):  
Álvaro Muñoz-López ◽  
Eddy. H.J. van Roon ◽  
Damià Romero-Moya ◽  
Belén López-Millan ◽  
Ronald W. Stam ◽  
...  
Leukemia ◽  
2015 ◽  
Vol 30 (3) ◽  
pp. 674-682 ◽  
Author(s):  
C Bueno ◽  
J L Sardina ◽  
B Di Stefano ◽  
D Romero-Moya ◽  
A Muñoz-López ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Yang Yang ◽  
Bin Liu ◽  
Jianwen Dong ◽  
Liangming Zhang ◽  
Mao Pang ◽  
...  

Induced pluripotent stem cells (iPSCs) are of great clinical interest for they are derived from one’s own somatic cells and have the potential of committed differentiation without immunological rejection after autografting. However, the use of viral and other modified vectors may still cause tumorigenesis due to chromosome insertion mutation, leading to limited practical use. iPSCs generated by reprogramming proteins overcome the potential safety risk and complicated manipulation procedures, thus they own better application prospective, yet some technical difficulties need to be studied and resolved, for instance, low reprogramming efficiency, unclear transduction, and reprogramming mechanism. In this paper, we summarize the current progress of proteins reprogramming technology for generation of iPSCs and discuss the promising efficiency-improved reprogramming methods by proteins plus other kinds of chemical compounds.


2016 ◽  
Vol 61 (2) ◽  
pp. 154-167 ◽  
Author(s):  
Chunyu Bai ◽  
Xiangchen Li ◽  
Yuhua Gao ◽  
Ziao Yuan ◽  
Pengfei Hu ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-10 ◽  
Author(s):  
Seung-Ick Oh ◽  
Chang Kyu Lee ◽  
Kyung Jin Cho ◽  
Kyung-Ok Lee ◽  
Ssang-Goo Cho ◽  
...  

Reprogramming of somatic cells into induced pluripotent stem cells (iPSCs) is achieved by viral-mediated transduction of defined transcription factors. Generation of iPSCs is of great medical interest as they have the potential to be a source of patient-specific cells. For the eventual goal of clinical application, it is necessary to overcome the limitations of low reprogramming efficiency and chromosomal abnormalities due to viral DNA integration. In this paper, we summarize the current state of reprogramming technology for generation of iPSCs and also discuss potential approaches to the development of safe iPSCs for personalized cell-based replacement therapy.


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