scholarly journals Surface geometry of poly(ether imide) boosts mouse pluripotent stem cell spontaneous cardiomyogenesis via modulating the embryoid body formation process

2017 ◽  
Vol 64 (3) ◽  
pp. 367-382 ◽  
Author(s):  
Xun Xu ◽  
Weiwei Wang ◽  
Zhengdong Li ◽  
Karl Kratz ◽  
Nan Ma ◽  
...  
2011 ◽  
Vol 5 (2) ◽  
pp. 022207 ◽  
Author(s):  
Feng Xu ◽  
BanuPriya Sridharan ◽  
ShuQi Wang ◽  
Umut Atakan Gurkan ◽  
Brian Syverud ◽  
...  

2013 ◽  
Vol 124 (1) ◽  
pp. E8-E14 ◽  
Author(s):  
Koshi Otsuki ◽  
Mitsuyoshi Imaizumi ◽  
Yukio Nomoto ◽  
Mika Nomoto ◽  
Ikuo Wada ◽  
...  

2007 ◽  
Vol 10 (2) ◽  
pp. 0-0 ◽  
Author(s):  
Uthayashanker R. Ezekiel ◽  
Mariappan Muthuchamy ◽  
Jan S. Ryerse ◽  
Rita M. Heuertz

2017 ◽  
Vol 41 (4) ◽  
pp. 1661-1674 ◽  
Author(s):  
Liang-Fang Zhu ◽  
Qiu-Ru Chen ◽  
Shao-Zhen Chen ◽  
Ling-Yan Wang ◽  
Xiao-Feng Luo ◽  
...  

Objective: The present study aimed to establish an induced pluripotent stem cell (iPSC) line from acute myelogenous leukemia (AML) cells in vitro and identify their biological characteristics. Methods: Cells from the AML-infiltrated skin from an M6 patient were infected with a lentivirus carrying OCT4, SOX2, KLF4 and C-MYC to induce iPSCs. The characteristics of the iPSCs were confirmed by alkaline phosphatase (ALP) staining. The proliferation ability of iPSCs was detected with a CCK-8 assay. The expression of pluripotency markers was measured by immunostaining, and the expression of stem cell-related genes was detected by qRT-PCR; distortion during the induction process was detected by karyotype analysis; the differentiation potential of iPSCs was determined by embryoid body-formation and teratoma-formation assays. ALP staining confirmed that these cells exhibited positive staining and had the characteristics of iPSCs. Results: The CCK-8 assay showed that the iPSCs had the ability to proliferate. Immunostaining demonstrated that iPSC clones showed positive expression of NANOG, SSEA-3, SSEA-4, TRA-1-60 and TRA-1-81. qRT-PCR results revealed that the mRNA expression of Nanog, Lin28, Cripto, FOX3, DNMT3b, DPPA2, and DPPA4 significantly increased in iPSCs. Karyotype analysis found no chromosome aberration in the iPSCs. The results of the embryoid body-formation and teratoma-formation assays indicated that the iPSCs had the potential to differentiate into all three germ layers. Conclusion: Our study provided evidence that an iPSC line derived from AML cells was successfully established.


Author(s):  
Dawn P. Spelke ◽  
Daniel Ortmann ◽  
Ali Khademhosseini ◽  
Lino Ferreira ◽  
Jeffrey M. Karp

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