| Literature DB >> 34300306 |
Hyerin Jung1,2, Yeri Alice Rim1,2, Narae Park1,2, Yoojun Nam3, Ji Hyeon Ju1,2,3,4.
Abstract
Osteogenesis imperfecta (OI) is a genetic disease characterized by bone fragility and repeated fractures. The bone fragility associated with OI is caused by a defect in collagen formation due to mutation of COL1A1 or COL1A2. Current strategies for treating OI are not curative. In this study, we generated induced pluripotent stem cells (iPSCs) from OI patient-derived blood cells harboring a mutation in the COL1A1 gene. Osteoblast (OB) differentiated from OI-iPSCs showed abnormally decreased levels of type I collagen and osteogenic differentiation ability. Gene correction of the COL1A1 gene using CRISPR/Cas9 recovered the decreased type I collagen expression in OBs differentiated from OI-iPSCs. The osteogenic potential of OI-iPSCs was also recovered by the gene correction. This study suggests a new possibility of treatment and in vitro disease modeling using patient-derived iPSCs and gene editing with CRISPR/Cas9.Entities:
Keywords: COL1A1; gene editing; induced pluripotent stem cell; osteoblast differentiation; osteogenesis imperfecta
Year: 2021 PMID: 34300306 DOI: 10.3390/jcm10143141
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241