| Autor: |
Uhlin E; Department of Neuroscience, Karolinska Institutet., Marin Navarro A; Department of Neuroscience, Karolinska Institutet; Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet., Rönnholm H; Department of Neuroscience, Karolinska Institutet., Day K; Department of Neuroscience, Karolinska Institutet., Kele M; Department of Neuroscience, Karolinska Institutet., Falk A; Department of Neuroscience, Karolinska Institutet; Anna.Falk@ki.se. |
| Abstrakt: |
Xeno-free and fully defined conditions are key parameters for robust and reproducible generation of homogenous human induced pluripotent stem (hiPS) cells. Maintenance of hiPS cells on feeder cells or undefined matrices are susceptible to batch variances, pathogenic contamination and risk of immunogenicity. Utilizing the defined recombinant human laminin 521 (LN-521) matrix in combination with xeno-free and defined media formulations reduces variability and allows for the consistent generation of hiPS cells. The Sendai virus (SeV) vector is a non-integrating RNA-based system, thus circumventing concerns associated with the potential disruptive effect on genome integrity integrating vectors can have. Furthermore, these vectors have demonstrated relatively high efficiency in the reprogramming of dermal fibroblasts. In addition, enzymatic single cell passaging of cells facilitates homogeneous maintenance of hiPS cells without substantial prior experience of stem cell culture. Here we describe a protocol that has been extensively tested and developed with a focus on reproducibility and ease of use, providing a robust and practical way to generate defined and xeno-free human hiPS cells from fibroblasts. |
