Literature DB >> 31893464

In vivo characterization of skeletal muscle function in nebulin-deficient mice.

Charlotte Gineste1, Augustin C Ogier2, Isabelle Varlet1, Zaynab Hourani3, Monique Bernard1, Henk Granzier3, David Bendahan1, Julien Gondin1,4.   

Abstract

INTRODUCTION: The conditional nebulin knockout mouse is a new model mimicking nemaline myopathy, a rare disease characterized by muscle weakness and rods within muscle fibers. We investigated the impact of nebulin (NEB) deficiency on muscle function in vivo.
METHODS: Conditional nebulin knockout mice and control littermates were studied at 10 to 12 months. Muscle function (force and fatigue) and anatomy (muscles volume and fat content) were measured in vivo. Myosin heavy chain (MHC) composition and nebulin (NEB) protein expression were assessed by protein electrophoresis.
RESULTS: Conditional nebulin knockout mice displayed a lower NEB level (-90%) leading to a 40% and 45% reduction in specific maximal force production and muscles volume, respectively. Nebulin deficiency was also associated with higher resistance to fatigue and increased MHC I content. DISCUSSION: Adult nebulin-deficient mice displayed severe muscle atrophy and weakness in vivo related to a low NEB content but an improved fatigue resistance due to a slower contractile phenotype.
© 2019 Wiley Periodicals, Inc.

Entities:  

Keywords:  zzm321990in vivo; fatigue; muscle wasting; muscle weakness; nemaline myopathy; neuromuscular disorder

Mesh:

Substances:

Year:  2020        PMID: 31893464      PMCID: PMC7393679          DOI: 10.1002/mus.26798

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  38 in total

1.  A novel ACTA1 mutation resulting in a severe congenital myopathy with nemaline bodies, intranuclear rods and type I fibre predominance.

Authors:  Gianina Ravenscroft; Jo M Wilmshurst; Komala Pillay; Padma Sivadorai; William Wallefeld; Kristen J Nowak; Nigel G Laing
Journal:  Neuromuscul Disord       Date:  2010-09-17       Impact factor: 4.296

2.  Hypertrophy and dietary tyrosine ameliorate the phenotypes of a mouse model of severe nemaline myopathy.

Authors:  Mai-Anh T Nguyen; Josephine E Joya; Anthony J Kee; Ana Domazetovska; Nan Yang; Jeff W Hook; Frances A Lemckert; Emma Kettle; Valentina A Valova; Philip J Robinson; Kathryn N North; Peter W Gunning; Christina A Mitchell; Edna C Hardeman
Journal:  Brain       Date:  2011-11-08       Impact factor: 13.501

3.  Nebulin-deficient mice exhibit shorter thin filament lengths and reduced contractile function in skeletal muscle.

Authors:  Marie-Louise Bang; Xiaodong Li; Ryan Littlefield; Shannon Bremner; Andrea Thor; Kirk U Knowlton; Richard L Lieber; Ju Chen
Journal:  J Cell Biol       Date:  2006-06-12       Impact factor: 10.539

4.  Nebulin regulates thin filament length, contractility, and Z-disk structure in vivo.

Authors:  Christian C Witt; Christoph Burkart; Dietmar Labeit; Mark McNabb; Yiming Wu; Henk Granzier; Siegfried Labeit
Journal:  EMBO J       Date:  2006-08-10       Impact factor: 11.598

Review 5.  Muscle imaging in congenital myopathies.

Authors:  Susana Quijano-Roy; Robert Y Carlier; Dirk Fischer
Journal:  Semin Pediatr Neurol       Date:  2011-12       Impact factor: 1.636

6.  Nebulin is a full-length template of actin filaments in the skeletal muscle sarcomere: an immunoelectron microscopic study of its orientation and span with site-specific monoclonal antibodies.

Authors:  J Wright; Q Q Huang; K Wang
Journal:  J Muscle Res Cell Motil       Date:  1993-10       Impact factor: 2.698

7.  Deleting exon 55 from the nebulin gene induces severe muscle weakness in a mouse model for nemaline myopathy.

Authors:  Coen A C Ottenheijm; Danielle Buck; Josine M de Winter; Claudia Ferrara; Nicoletta Piroddi; Chiara Tesi; Jeffrey R Jasper; Fady I Malik; Hui Meng; Ger J M Stienen; Alan H Beggs; Siegfried Labeit; Corrado Poggesi; Michael W Lawlor; Henk Granzier
Journal:  Brain       Date:  2013-05-28       Impact factor: 13.501

8.  Altered myofilament function depresses force generation in patients with nebulin-based nemaline myopathy (NEM2).

Authors:  Coen A C Ottenheijm; Pleuni Hooijman; Elizabeth T DeChene; Ger J Stienen; Alan H Beggs; Henk Granzier
Journal:  J Struct Biol       Date:  2009-11-26       Impact factor: 2.867

9.  Magnetic resonance imaging findings of the skeletal muscle of a patient with nemaline myopathy.

Authors:  M Oishi; Y Mochizuki
Journal:  Intern Med       Date:  1998-09       Impact factor: 1.271

10.  Thin filament length dysregulation contributes to muscle weakness in nemaline myopathy patients with nebulin deficiency.

Authors:  Coen A C Ottenheijm; Christian C Witt; Ger J Stienen; Siegfried Labeit; Alan H Beggs; Henk Granzier
Journal:  Hum Mol Genet       Date:  2009-04-04       Impact factor: 6.150

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  2 in total

1.  Impaired aerobic capacity and premature fatigue preceding muscle weakness in the skeletal muscle Tfam-knockout mouse model.

Authors:  Benjamin Chatel; Sylvie Ducreux; Zeina Harhous; Nadia Bendridi; Isabelle Varlet; Augustin C Ogier; Monique Bernard; Julien Gondin; Jennifer Rieusset; Håkan Westerblad; David Bendahan; Charlotte Gineste
Journal:  Dis Model Mech       Date:  2021-09-15       Impact factor: 5.758

2.  Integrative Analysis of Nanopore and Illumina Sequencing Reveals Alternative Splicing Complexity in Pig Longissimus Dorsi Muscle.

Authors:  Ze Shu; Ligang Wang; Jinbu Wang; Longchao Zhang; Xinhua Hou; Hua Yan; Lixian Wang
Journal:  Front Genet       Date:  2022-04-11       Impact factor: 4.772

  2 in total

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