scholarly journals Bovine trophectoderm cells induced from bovine fibroblasts with induced pluripotent stem cell reprogramming factors

2017 ◽  
Vol 84 (6) ◽  
pp. 468-485 ◽  
Author(s):  
Neil C. Talbot ◽  
Wendy O. Sparks ◽  
Caitlin E. Phillips ◽  
Alan D. Ealy ◽  
Anne M. Powell ◽  
...  
2015 ◽  
Vol 23 (5) ◽  
pp. 952-963 ◽  
Author(s):  
Ashley L Fritz ◽  
Maroof M Adil ◽  
Sunnie R Mao ◽  
David V Schaffer

Stem Cells ◽  
2012 ◽  
Vol 30 (11) ◽  
pp. 2596-2601 ◽  
Author(s):  
Lucas V. Greder ◽  
Sandeep Gupta ◽  
Shunan Li ◽  
Md. Joynal Abedin ◽  
Abdulrahim Sajini ◽  
...  

Stem Cells ◽  
2013 ◽  
Vol 31 (4) ◽  
pp. 682-692 ◽  
Author(s):  
Yun-Shen Chan ◽  
Jonathan Göke ◽  
Xinyi Lu ◽  
Nandini Venkatesan ◽  
Bo Feng ◽  
...  

2019 ◽  
Vol 6 (2) ◽  
pp. 75-86 ◽  
Author(s):  
Ignacio Rodriguez-Polo ◽  
Michael Stauske ◽  
Alexander Becker ◽  
Iris Bartels ◽  
Ralf Dressel ◽  
...  

Abstract. Clinical application of regenerative therapies using embryonic or induced pluripotent stem cells is within reach. Progress made during recent years has encouraged researchers to address remaining open questions in order to finally translate experimental cell replacement therapies into application in patients. To achieve this, studies in translationally relevant animal models are required to make the final step to the clinic. In this context, the baboon (Papio anubis) may represent a valuable nonhuman primate (NHP) model to test cell replacement therapies because of its close evolutionary relationship to humans and its large body size. In this study, we describe the reprogramming of adult baboon skin fibroblasts using the piggyBac transposon system. Via transposon-mediated overexpression of six reprogramming factors, we generated five baboon induced pluripotent stem cell (iPSC) lines. The iPSC lines were characterized with respect to alkaline phosphatase activity, pluripotency factor expression analysis, teratoma formation potential, and karyotype. Furthermore, after initial cocultivation with mouse embryonic fibroblasts, we were able to adapt iPSC lines to feeder-free conditions. In conclusion, we established a robust and efficient protocol for iPSC generation from adult baboon fibroblasts.


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