Cell transplantation-mediated dystrophin supplementation efficacy in Duchenne muscular dystrophy mouse motor function improvement demonstrated by enhanced skeletal muscle fatigue tolerance

Cell therapy-mediated dystrophin supplementation efficiently improved DMD muscle functions, as evaluated using newly developed evaluation methods. The enhanced muscle fatigue tolerance in 21-week-old mice was associated with the preferential regeneration of damage-resistant and oxidative fibers, highlighting increased mitochondrial activity, after cell transplantation. These findings significantly contribute to a more in-depth understanding of DMD pathogenesis.

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Publication Details

Journal
Stem Cell Research & Therapy
Published
2024-09-19
DOI
https://doi.org/10.1186/s13287-024-03922-x
Citations
2
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.47

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article

Cell transplantation-mediated dystrophin supplementation efficacy in Duchenne muscular dystrophy mouse motor function improvement demonstrated by enhanced skeletal muscle fatigue tolerance

Masamichi Yamamoto, Clémence Kiho Bourgeois Yoshioka, Hidetoshi Sakurai, Megumi Goto et al.
2 citations
Stem Cell Research & Therapy
Muscle Physiology and Disorders
0.47
article

Cell transplantation-mediated dystrophin supplementation efficacy in Duchenne muscular dystrophy mouse motor function improvement demonstrated by enhanced skeletal muscle fatigue tolerance

Masamichi Yamamoto, Clémence Kiho Bourgeois Yoshioka, Hidetoshi Sakurai, Megumi Goto, Daiki Watanabe, Nana Takenaka-Ninagawa, Tomoki Aoyama, M Miki
article en
2 citations

Abstract

Cell therapy-mediated dystrophin supplementation efficiently improved DMD muscle functions, as evaluated using newly developed evaluation methods. The enhanced muscle fatigue tolerance in 21-week-old mice was associated with the preferential regeneration of damage-resistant and oxidative fibers, highlighting increased mitochondrial activity, after cell transplantation. These findings significantly contribute to a more in-depth understanding of DMD pathogenesis.

Stem Cell Research & TherapyVol. 15(1)
Osaka University of Health and Sport Sciences (JP), Kyoto University (JP), Nagoya City University (JP), National Cerebral and Cardiovascular Center (JP), Kyoto University Hospital (JP)
Japan Agency for Medical Research and Development, Research Center Network for Realization of Regenerative Medicine, Japan Society for the Promotion of Science
Zero hunger
Openalex Percentile: Top 35%
Muscle Physiology and Disorders
0.47
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