TY - JOUR
T1 - Low dose resveratrol ameliorates mitochondrial respiratory dysfunction and enhances cellular reprogramming
AU - Mizuguchi, Yuki
AU - Hatakeyama, Hideyuki
AU - Sueoka, Kou
AU - Tanaka, Mamoru
AU - Goto, Yu ichi
N1 - Funding Information:
This study was financially supported in part by Grant-in-Aid for Research on Intractable Diseases (Mitochondrial Disorders) from the Ministry of Health, Labour, and Welfare, Japan; by AMED-CREST from the Japan Agency for Medical Research and Development. The authors declare that they have no conflict of interest concerning this study.
Publisher Copyright:
© 2017 Elsevier B.V. and Mitochondria Research Society
Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 2017/5/1
Y1 - 2017/5/1
N2 - Mitochondrial disease is associated with a wide variety of clinical presentations, even among patients carrying heteroplasmic mitochondrial DNA (mtDNA) mutations, probably because of variations in mutant mtDNA proportions at the tissue and organ levels. Although several case reports and clinical trials have assessed the effectiveness of various types of drugs and supplements for the treatment of mitochondrial diseases, there are currently no cures for these conditions. In this study, we demonstrated for the first time that low dose resveratrol (RSV) ameliorated mitochondrial respiratory dysfunction in patient-derived fibroblasts carrying homoplasmic mtDNA mutations. Furthermore, low dose RSV also facilitated efficient cellular reprogramming of the patient-derived fibroblasts into induced pluripotent stem cells, partly due to improved cellular viability. Our results highlight the potential of RSV as a new therapeutic drug candidate for the treatment of mitochondrial diseases.
AB - Mitochondrial disease is associated with a wide variety of clinical presentations, even among patients carrying heteroplasmic mitochondrial DNA (mtDNA) mutations, probably because of variations in mutant mtDNA proportions at the tissue and organ levels. Although several case reports and clinical trials have assessed the effectiveness of various types of drugs and supplements for the treatment of mitochondrial diseases, there are currently no cures for these conditions. In this study, we demonstrated for the first time that low dose resveratrol (RSV) ameliorated mitochondrial respiratory dysfunction in patient-derived fibroblasts carrying homoplasmic mtDNA mutations. Furthermore, low dose RSV also facilitated efficient cellular reprogramming of the patient-derived fibroblasts into induced pluripotent stem cells, partly due to improved cellular viability. Our results highlight the potential of RSV as a new therapeutic drug candidate for the treatment of mitochondrial diseases.
KW - Mitochondrial disease
KW - Mitochondrial respiratory dysfunction
KW - Patient-derived induced pluripotent stem cells (iPSCs)
KW - Resveratrol
UR - http://www.scopus.com/inward/record.url?scp=85009881987&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85009881987&partnerID=8YFLogxK
U2 - 10.1016/j.mito.2016.12.006
DO - 10.1016/j.mito.2016.12.006
M3 - Article
C2 - 28093354
AN - SCOPUS:85009881987
SN - 1567-7249
VL - 34
SP - 43
EP - 48
JO - Mitochondrion
JF - Mitochondrion
ER -