| Literature DB >> 31090270 |
Shuang-Yi Hu1, Qian-Qian Zhuang1, Yue Qiu1, Xu-Fen Zhu1, Qing-Feng Yan1,2,3.
Abstract
Mitochondrion is a semi-autonomous organelle, important for cell energy metabolism, apoptosis, the production of reactive oxygen species (ROS), and Ca2+ homeostasis. Mitochondrial DNA (mtDNA) mutation is one of the primary factors in mitochondrial disorders. Though much progress has been made, there remain many difficulties in constructing cell models for mitochondrial diseases. This seriously restricts studies related to targeted drug discovery and the mechanism and therapy for such diseases. Here we summarize the characteristics of patient-specific immortalized lymphoblastoid cells, fibroblastoid cells, cytoplasmic hybrid (cybrid) cell lines, and induced pluripotent stem cells (iPSCs)-derived differentiation cells in the study of mitochondrial disorders, as well as offering discussion of roles and advances of these cell models, particularly in the screening of drugs.Entities:
Keywords: Mitochondrial diseases; Mitochondrial DNA; Cell model; Drug discovery
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Year: 2019 PMID: 31090270 PMCID: PMC6568230 DOI: 10.1631/jzus.B1900196
Source DB: PubMed Journal: J Zhejiang Univ Sci B ISSN: 1673-1581 Impact factor: 3.066