Gene-repaired iPS cells as novel approach for patient with osteogenesis imperfecta

基因修复 iPS 细胞作为成骨不全症患者的新治疗方法

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作者:Agnieszka Fus-Kujawa, Barbara Mendrek, Karolina Bajdak-Rusinek, Natalia Diak, Karolina Strzelec, Ewa Gutmajster, Kamil Janelt, Agnieszka Kowalczuk, Anna Trybus, Patrycja Rozwadowska, Wojciech Wojakowski, Katarzyna Gawron, Aleksander L Sieroń

Discussion

The use of novel polymer Poly[N,N-Dimethylaminoethyl Methacrylate-co-Hydroxyl-Bearing Oligo(Ethylene Glycol) Methacrylate] Arms (P(DMAEMA-co-OEGMA-OH) with star-like structure has been shown as an efficient tool for nucleic acids delivery into cells (Funded by National Science Centre, Contract No. UMO-2020/37/N/NZ2/01125).

Methods

In this controlled trial, fibroblasts derived from patient diagnosed with OI type II have been successfully reprogrammed into induced Pluripotent Stem cells (iPSCs) using Yamanaka factors. Those cells were subjected to repair mutations found in the COL1A1 gene using homologous recombination (HR) approach facilitated with star polymer (STAR) as a carrier of the genetic material.

Results

Delivery of the correct linear DNA fragment to the osteogenesis imperfecta patient's cells resulted in the repair of the DNA mutation with an 84% success rate. IPSCs showed 87% viability after STAR treatment and 82% with its polyplex.

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