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. 2018 Mar 23;8:5118. doi: 10.1038/s41598-018-23175-y

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Overexpression of FXN and ISCU, but not TfR1, in Irp1 or 2 deficient MEFs improves the mitochondrial quality. MEFs were stained with Mito-tracker and analysed by Flow cytometry to represent the mitochondrial membrane potential (MMP) 24 h post transfection with plasmids pcDNA3.1-FXN-myc and pXS-ISCU-myc (a) or pcMV3-TfR1 (b). A representative graph is presented. (c) Relative mitochondrial DNA copy number after co-overexpression of FXN and ISCU in Irp ablation cells. n = 3, each duplicates. *p < 0.05, **p < 0.01 compared with WT.