scholarly journals 504. Targeted Genome Engineering of Induced Pluripotent Stem Cells To Produce Auto-Regulated Inflammation Resistance for Musculoskeletal Regenerative Medicine

2015 ◽  
Vol 23 ◽  
pp. S201-S202
Author(s):  
Jonathan M. Brunger ◽  
Ananya Zutshi ◽  
Vincent P. Willard ◽  
Charles A. Gersbach ◽  
Farshid Guilak
2013 ◽  
Vol 2 (1) ◽  
pp. 2:5 ◽  
Author(s):  
Renli Ru ◽  
Yongchao Yao ◽  
Songlin Yu ◽  
Benpeng Yin ◽  
Wanwan Xu ◽  
...  

2011 ◽  
Vol 2 (1) ◽  
pp. 1-6 ◽  
Author(s):  
Yuh-Chi Chen ◽  
Kung-Lin Tsai ◽  
Chia-Wei Hung ◽  
Dah-Ching Ding ◽  
Lih-Hsin Chen ◽  
...  

2019 ◽  
Vol 8 (11) ◽  
pp. 1782 ◽  
Author(s):  
Antonio Palladino ◽  
Isabella Mavaro ◽  
Carmela Pizzoleo ◽  
Elena De Felice ◽  
Carla Lucini ◽  
...  

Tissue engineering (TE) pursues the ambitious goal to heal damaged tissues. One of the most successful TE approaches relies on the use of scaffolds specifically designed and fabricated to promote tissue growth. During regeneration the guidance of biological events may be essential to sustain vasculature neoformation inside the engineered scaffold. In this context, one of the most effective strategies includes the incorporation of vasculature forming cells, namely endothelial cells (EC), into engineered constructs. However, the most common EC sources currently available, intended as primary cells, are affected by several limitations that make them inappropriate to personalized medicine. Human induced Pluripotent Stem Cells (hiPSC), since the time of their discovery, represent an unprecedented opportunity for regenerative medicine applications. Unfortunately, human induced Pluripotent Stem Cells-Endothelial Cells (hiPSC-ECs) still display significant safety issues. In this work, we reviewed the most effective protocols to induce pluripotency, to generate cells displaying the endothelial phenotype and to perform an efficient and safe cell selection. We also provide noteworthy examples of both in vitro and in vivo applications of hiPSC-ECs in order to highlight their ability to form functional blood vessels. In conclusion, we propose hiPSC-ECs as the preferred source of endothelial cells currently available in the field of personalized regenerative medicine.


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