| Literature DB >> 27166949 |
Ting-Hsiang Wu1, Enrico Sagullo2, Dana Case2, Xin Zheng2, Yanjing Li2, Jason S Hong2, Tara TeSlaa3, Alexander N Patananan2, J Michael McCaffery4, Kayvan Niazi5, Daniel Braas6, Carla M Koehler7, Thomas G Graeber8, Pei-Yu Chiou9, Michael A Teitell10.
Abstract
mtDNA sequence alterations are challenging to generate but desirable for basic studies and potential correction of mtDNA diseases. Here, we report a new method for transferring isolated mitochondria into somatic mammalian cells using a photothermal nanoblade, which bypasses endocytosis and cell fusion. The nanoblade rescued the pyrimidine auxotroph phenotype and respiration of ρ0 cells that lack mtDNA. Three stable isogenic nanoblade-rescued clones grown in uridine-free medium showed distinct bioenergetics profiles. Rescue lines 1 and 3 reestablished nucleus-encoded anapleurotic and catapleurotic enzyme gene expression patterns and had metabolite profiles similar to the parent cells from which the ρ0 recipient cells were derived. By contrast, rescue line 2 retained a ρ0 cell metabolic phenotype despite growth in uridine-free selection. The known influence of metabolite levels on cellular processes, including epigenome modifications and gene expression, suggests metabolite profiling can help assess the quality and function of mtDNA-modified cells.Entities:
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Year: 2016 PMID: 27166949 PMCID: PMC5062745 DOI: 10.1016/j.cmet.2016.04.007
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287