| Literature DB >> 33422359 |
Alexander J Sercel1, Natasha M Carlson2, Alexander N Patananan3, Michael A Teitell4.
Abstract
Mammalian cells, with the exception of erythrocytes, harbor mitochondria, which are organelles that provide energy, intermediate metabolites, and additional activities to sustain cell viability, replication, and function. Mitochondria contain multiple copies of a circular genome called mitochondrial DNA (mtDNA), whose individual sequences are rarely identical (homoplasmy) because of inherited or sporadic mutations that result in multiple mtDNA genotypes (heteroplasmy). Here, we examine potential mechanisms for maintenance or shifts in heteroplasmy that occur in induced pluripotent stem cells (iPSCs) generated by cellular reprogramming, and further discuss manipulations that can alter heteroplasmy to impact stem and differentiated cell performance. This additional insight will assist in developing more robust iPSC-based models of disease and differentiated cell therapies.Entities:
Keywords: heteroplasmy; induced pluripotent stem cell; mitochondrial DNA; pluripotency; reprogramming
Mesh:
Substances:
Year: 2021 PMID: 33422359 PMCID: PMC7954944 DOI: 10.1016/j.tcb.2020.12.009
Source DB: PubMed Journal: Trends Cell Biol ISSN: 0962-8924 Impact factor: 21.167