DOK7 gene therapy benefits mouse models of diseases characterized by defects in the neuromuscular junction

Author:

Arimura Sumimasa1,Okada Takashi2,Tezuka Tohru1,Chiyo Tomoko2,Kasahara Yuko2,Yoshimura Toshiro3,Motomura Masakatsu4,Yoshida Nobuaki5,Beeson David6,Takeda Shin’ichi2,Yamanashi Yuji1

Affiliation:

1. Division of Genetics, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

2. Department of Molecular Therapy, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.

3. Department of Occupational Therapy, Nagasaki University School of Health Sciences, Nagasaki, Japan.

4. Department of Electrical and Electronics Engineering, Faculty of Engineering, Nagasaki Institute of Applied Science, Nagasaki, Japan.

5. Laboratory of Developmental Genetics, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.

6. Neurosciences Group, Weatherall Institute of Molecular Medicine, University of Oxford, Oxford, UK.

Abstract

Building connections by gene therapy Voluntary movement requires a molecular conversation between nerves and muscles. This conversation occurs at the neuromuscular junction, a structure where nerves and muscle physically connect. People with diseases characterized by muscle weakness have aberrantly small neuromuscular junctions. Arimura et al. used gene therapy to enlarge the neuromuscular junction, which made muscles stronger. Studying mouse models of two distinct neuromuscular disorders, they used an adenovirus vector to deliver DOK7 , a gene required for formation of the neuromuscular junction. The therapy improved the mice's motor activity and life span. Science , this issue p. 1505

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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