Sanfilippo syndrome type B: Reprogramming cultured skin fibroblasts to induced pluripotent stem cells using non-integrating Sendai virus vector

2015 ◽  
Vol 114 (2) ◽  
pp. S118
Author(s):  
Kelly A. Turner ◽  
Francis Y. Choy
PLoS ONE ◽  
2012 ◽  
Vol 7 (8) ◽  
pp. e42855 ◽  
Author(s):  
Mizuho Ono ◽  
Yuko Hamada ◽  
Yasue Horiuchi ◽  
Mami Matsuo-Takasaki ◽  
Yoshimasa Imoto ◽  
...  

2018 ◽  
Vol 27 (22) ◽  
pp. 1577-1586 ◽  
Author(s):  
Masaya Tsukamoto ◽  
Toshiya Nishimura ◽  
Kyohei Yodoe ◽  
Ryoji Kanegi ◽  
Yasunori Tsujimoto ◽  
...  

2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Chad C. MacArthur ◽  
Andrew Fontes ◽  
Namritha Ravinder ◽  
David Kuninger ◽  
Jasmeet Kaur ◽  
...  

The generation of induced pluripotent stem cells (iPSCs) from somatic cells has enabled the possibility of providing unprecedented access to patient-specific iPSC cells for drug screening, disease modeling, and cell therapy applications. However, a major obstacle to the use of iPSC for therapeutic applications is the potential of genomic modifications caused by insertion of viral transgenes in the cellular genome. A second concern is that reprogramming often requires the use of animal feeder layers and reagents that contain animal origin products, which hinder the generation of clinical-grade iPSCs. Here, we report the generation of iPSCs by an RNA Sendai virus vector that does not integrate into the cells genome, providing transgene-free iPSC line. In addition, reprogramming can be performed in feeder-free condition with StemPro hESC SFM medium and in xeno-free (XF) conditions. Generation of an integrant-free iPSCs generated in xeno-free media should facilitate the safe downstream applications of iPSC-based cell therapies.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Johanna Geuder ◽  
Lucas E. Wange ◽  
Aleksandar Janjic ◽  
Jessica Radmer ◽  
Philipp Janssen ◽  
...  

AbstractComparing the molecular and cellular properties among primates is crucial to better understand human evolution and biology. However, it is difficult or ethically impossible to collect matched tissues from many primates, especially during development. An alternative is to model different cell types and their development using induced pluripotent stem cells (iPSCs). These can be generated from many tissue sources, but non-invasive sampling would decisively broaden the spectrum of non-human primates that can be investigated. Here, we report the generation of primate iPSCs from urine samples. We first validate and optimize the procedure using human urine samples and show that suspension- Sendai Virus transduction of reprogramming factors into urinary cells efficiently generates integration-free iPSCs, which maintain their pluripotency under feeder-free culture conditions. We demonstrate that this method is also applicable to gorilla and orangutan urinary cells isolated from a non-sterile zoo floor. We characterize the urinary cells, iPSCs and derived neural progenitor cells using karyotyping, immunohistochemistry, differentiation assays and RNA-sequencing. We show that the urine-derived human iPSCs are indistinguishable from well characterized PBMC-derived human iPSCs and that the gorilla and orangutan iPSCs are well comparable to the human iPSCs. In summary, this study introduces a novel and efficient approach to non-invasively generate iPSCs from primate urine. This will extend the zoo of species available for a comparative approach to molecular and cellular phenotypes.


2019 ◽  
Vol 40 (23) ◽  
pp. 1832-1836 ◽  
Author(s):  
Peter J Schwartz ◽  
Massimiliano Gnecchi ◽  
Federica Dagradi ◽  
Silvia Castelletti ◽  
Gianfranco Parati ◽  
...  

2018 ◽  
Vol 27 (4) ◽  
pp. 287-295 ◽  
Author(s):  
Alberto La Spada ◽  
Aikaterini Ntai ◽  
Stefano Genovese ◽  
Maurizio Rondinelli ◽  
Pasquale De Blasio ◽  
...  

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