Literature DB >> 21194022

Monitoring murine skeletal muscle function for muscle gene therapy.

Chady H Hakim1, Dejia Li, Dongsheng Duan.   

Abstract

The primary function of skeletal muscle is to generate force. Muscle force production is compromised in various forms of acquired and/or inherited muscle diseases. An important goal of muscle gene therapy is to recover muscle strength. Genetically engineered mice and spontaneous mouse mutants are readily available for preclinical muscle gene therapy studies. In this chapter, we outlined the methods commonly used for measuring murine skeletal muscle function. These include ex vivo and in situ analysis of the contractile profile of a single intact limb muscle (the extensor digitorium longus for ex vivo assay and the tibialis anterior muscle for in situ assay), grip force analysis, and downhill treadmill exercise. Force measurement in a single muscle is extremely useful for pilot testing of new gene therapy protocols by local gene transfer. Grip force and treadmill assessments offer body-wide evaluation following systemic muscle gene therapy.

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Year:  2011        PMID: 21194022      PMCID: PMC3118041          DOI: 10.1007/978-1-61737-982-6_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  23 in total

1.  Force and power output of fast and slow skeletal muscles from mdx mice 6-28 months old.

Authors:  G S Lynch; R T Hinkle; J S Chamberlain; S V Brooks; J A Faulkner
Journal:  J Physiol       Date:  2001-09-01       Impact factor: 5.182

Review 2.  Striated muscle cytoarchitecture: an intricate web of form and function.

Authors:  Kathleen A Clark; Abigail S McElhinny; Mary C Beckerle; Carol C Gregorio
Journal:  Annu Rev Cell Dev Biol       Date:  2002-04-02       Impact factor: 13.827

3.  For a pragmatic approach to exercise studies.

Authors:  Christoph Handschin; Serge Summermatter; Nathan K LeBrasseur; Jiandie Lin; Bruce M Spiegelman
Journal:  J Appl Physiol (1985)       Date:  2010-01

4.  Interstrain variation in murine aerobic capacity.

Authors:  J T Lightfoot; M J Turner; K A Debate; S R Kleeberger
Journal:  Med Sci Sports Exerc       Date:  2001-12       Impact factor: 5.411

5.  Differential effects of dystrophin and utrophin gene transfer in immunocompetent muscular dystrophy (mdx) mice.

Authors:  S Ebihara; G H Guibinga; R Gilbert; J Nalbantoglu; B Massie; G Karpati; B J Petrof
Journal:  Physiol Genomics       Date:  2000-09-08       Impact factor: 3.107

6.  Tibialis anterior muscles in mdx mice are highly susceptible to contraction-induced injury.

Authors:  C Dellorusso; R W Crawford; J S Chamberlain; S V Brooks
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

7.  Modular flexibility of dystrophin: implications for gene therapy of Duchenne muscular dystrophy.

Authors:  Scott Q Harper; Michael A Hauser; Christiana DelloRusso; Dongsheng Duan; Robert W Crawford; Stephanie F Phelps; Hollie A Harper; Ann S Robinson; John F Engelhardt; Susan V Brooks; Jeffrey S Chamberlain
Journal:  Nat Med       Date:  2002-03       Impact factor: 53.440

8.  Fast-twitch skeletal muscles of dystrophic mouse pups are resistant to injury from acute mechanical stress.

Authors:  Robert W Grange; Thomas G Gainer; Krista M Marschner; Robert J Talmadge; James T Stull
Journal:  Am J Physiol Cell Physiol       Date:  2002-10       Impact factor: 4.249

9.  Cardiac expression of a mini-dystrophin that normalizes skeletal muscle force only partially restores heart function in aged Mdx mice.

Authors:  Brian Bostick; Yongping Yue; Chun Long; Nate Marschalk; Deborah M Fine; Jing Chen; Dongsheng Duan
Journal:  Mol Ther       Date:  2008-12-09       Impact factor: 11.454

10.  Ectopic catalase expression in mitochondria by adeno-associated virus enhances exercise performance in mice.

Authors:  Dejia Li; Yi Lai; Yongping Yue; Peter S Rabinovitch; Chady Hakim; Dongsheng Duan
Journal:  PLoS One       Date:  2009-08-19       Impact factor: 3.240

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  35 in total

1.  AAV CRISPR editing rescues cardiac and muscle function for 18 months in dystrophic mice.

Authors:  Chady H Hakim; Nalinda B Wasala; Christopher E Nelson; Lakmini P Wasala; Yongping Yue; Jacqueline A Louderman; Thais B Lessa; Aihua Dai; Keqing Zhang; Gregory J Jenkins; Michael E Nance; Xiufang Pan; Kasun Kodippili; N Nora Yang; Shi-Jie Chen; Charles A Gersbach; Dongsheng Duan
Journal:  JCI Insight       Date:  2018-12-06

2.  Disruption of KATP channel expression in skeletal muscle by targeted oligonucleotide delivery promotes activity-linked thermogenesis.

Authors:  Siva Rama Krishna Koganti; Zhiyong Zhu; Ekaterina Subbotina; Zhan Gao; Ana Sierra; Manuel Proenza; Liping Yang; Alexey Alekseev; Denice Hodgson-Zingman; Leonid Zingman
Journal:  Mol Ther       Date:  2015-02-04       Impact factor: 11.454

3.  Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice.

Authors:  Chady H Hakim; Dean J Burkin; Dongsheng Duan
Journal:  J Appl Physiol (1985)       Date:  2013-08-29

4.  Single SERCA2a Therapy Ameliorated Dilated Cardiomyopathy for 18 Months in a Mouse Model of Duchenne Muscular Dystrophy.

Authors:  Nalinda B Wasala; Yongping Yue; William Lostal; Lakmini P Wasala; Nandita Niranjan; Roger J Hajjar; Gopal J Babu; Dongsheng Duan
Journal:  Mol Ther       Date:  2020-01-10       Impact factor: 11.454

5.  Genomic removal of a therapeutic mini-dystrophin gene from adult mice elicits a Duchenne muscular dystrophy-like phenotype.

Authors:  Nalinda B Wasala; Yi Lai; Jin-Hong Shin; Junling Zhao; Yongping Yue; Dongsheng Duan
Journal:  Hum Mol Genet       Date:  2016-04-22       Impact factor: 6.150

6.  Orai1 enhances muscle endurance by promoting fatigue-resistant type I fiber content but not through acute store-operated Ca2+ entry.

Authors:  Ellie M Carrell; Aundrea R Coppola; Helen J McBride; Robert T Dirksen
Journal:  FASEB J       Date:  2016-09-01       Impact factor: 5.191

7.  Gender differences in contractile and passive properties of mdx extensor digitorum longus muscle.

Authors:  Chady H Hakim; Dongsheng Duan
Journal:  Muscle Nerve       Date:  2012-02       Impact factor: 3.217

8.  Dmpk gene deletion or antisense knockdown does not compromise cardiac or skeletal muscle function in mice.

Authors:  Samuel T Carrell; Ellie M Carrell; David Auerbach; Sanjay K Pandey; C Frank Bennett; Robert T Dirksen; Charles A Thornton
Journal:  Hum Mol Genet       Date:  2016-08-13       Impact factor: 6.150

9.  Truncated dystrophins reduce muscle stiffness in the extensor digitorum longus muscle of mdx mice.

Authors:  Chady H Hakim; Dongsheng Duan
Journal:  J Appl Physiol (1985)       Date:  2012-12-06

10.  Microdystrophin ameliorates muscular dystrophy in the canine model of duchenne muscular dystrophy.

Authors:  Jin-Hong Shin; Xiufang Pan; Chady H Hakim; Hsiao T Yang; Yongping Yue; Keqing Zhang; Ronald L Terjung; Dongsheng Duan
Journal:  Mol Ther       Date:  2013-01-15       Impact factor: 11.454

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