Literature DB >> 29658931

Optical Cross-Sectional Muscle Area Determination of Drosophila Melanogaster Adult Indirect Flight Muscles.

Estela Selma-Soriano1, Rubén Artero2, Beatriz Llamusi1.   

Abstract

Muscle mass wasting, known as muscle atrophy, is a common phenotype in Drosophila models of neuromuscular diseases. We have used the indirect flight muscles (IFMs) of flies, specifically the dorso-longitudinal muscles (DLM), as the experimental subject to measure the atrophic phenotype brought about by different genetic causes. In this protocol, we describe how to embed fly thorax muscles for semi thin sectioning, how to obtain a good contrast between muscle and the surrounding tissue, and how to process optical microscope images for semiautomatic acquisition of quantifiable data and analysis. We describe three specific applications of the methodological pipeline. First, we show how the method can be applied to quantify muscle degeneration in a myotonic dystrophy fly model; second, measurement of muscle cross-sectional area can help to identify genes that either promote or prevent muscle atrophy and/or muscle degeneration; third, this protocol can be applied to determine whether a candidate compound is able to significantly modify a given atrophic phenotype induced by a disease-causing mutation or by an environmental trigger.

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Year:  2018        PMID: 29658931      PMCID: PMC5933293          DOI: 10.3791/56179

Source DB:  PubMed          Journal:  J Vis Exp        ISSN: 1940-087X            Impact factor:   1.355


  9 in total

1.  Cell fate in the Drosophila ommatidium.

Authors:  A Tomlinson; D F Ready
Journal:  Dev Biol       Date:  1987-09       Impact factor: 3.582

2.  In vivo discovery of a peptide that prevents CUG-RNA hairpin formation and reverses RNA toxicity in myotonic dystrophy models.

Authors:  Amparo García-López; Beatriz Llamusí; Mar Orzáez; Enrique Pérez-Payá; Ruben D Artero
Journal:  Proc Natl Acad Sci U S A       Date:  2011-07-05       Impact factor: 11.205

3.  An improved method for accurate and rapid measurement of flight performance in Drosophila.

Authors:  Daniel T Babcock; Barry Ganetzky
Journal:  J Vis Exp       Date:  2014-02-13       Impact factor: 1.355

Review 4.  Flightless flies: Drosophila models of neuromuscular disease.

Authors:  Thomas E Lloyd; J Paul Taylor
Journal:  Ann N Y Acad Sci       Date:  2010-01       Impact factor: 5.691

5.  Drosophila Dystrophin is required for integrity of the musculature.

Authors:  Mariska C van der Plas; Gonneke S K Pilgram; Anja W M de Jong; Monique R K S Bansraj; Lee G Fradkin; Jasprina N Noordermeer
Journal:  Mech Dev       Date:  2007-04-21       Impact factor: 1.882

6.  Patterning the dorsal longitudinal flight muscles (DLM) of Drosophila: insights from the ablation of larval scaffolds.

Authors:  J J Fernandes; H Keshishian
Journal:  Development       Date:  1996-12       Impact factor: 6.868

7.  Increased autophagy and apoptosis contribute to muscle atrophy in a myotonic dystrophy type 1 Drosophila model.

Authors:  Ariadna Bargiela; Estefanía Cerro-Herreros; Juan M Fernandez-Costa; Juan J Vilchez; Beatriz Llamusi; Ruben Artero
Journal:  Dis Model Mech       Date:  2015-07-01       Impact factor: 5.758

8.  Development of the indirect flight muscles of Drosophila.

Authors:  J Fernandes; M Bate; K Vijayraghavan
Journal:  Development       Date:  1991-09       Impact factor: 6.868

9.  Muscleblind, BSF and TBPH are mislocalized in the muscle sarcomere of a Drosophila myotonic dystrophy model.

Authors:  Beatriz Llamusi; Ariadna Bargiela; Juan M Fernandez-Costa; Amparo Garcia-Lopez; Raffaella Klima; Fabian Feiguin; Ruben Artero
Journal:  Dis Model Mech       Date:  2012-11-01       Impact factor: 5.758

  9 in total
  3 in total

1.  Flight muscles degenerate by programmed cell death after migration in the wheat aphid, Sitobion avenae.

Authors:  Honglin Feng; Xiao Guo; Hongyan Sun; Shuai Zhang; Jinghui Xi; Jiao Yin; Yazhong Cao; Kebin Li
Journal:  BMC Res Notes       Date:  2019-10-21

2.  Rabphilin involvement in filtration and molecular uptake in Drosophila nephrocytes suggests a similar role in human podocytes.

Authors:  Estela Selma-Soriano; Beatriz Llamusi; Juan Manuel Fernández-Costa; Lauren Louise Ozimski; Rubén Artero; Josep Redón
Journal:  Dis Model Mech       Date:  2020-09-21       Impact factor: 5.758

3.  Defined D-hexapeptides bind CUG repeats and rescue phenotypes of myotonic dystrophy myotubes in a Drosophila model of the disease.

Authors:  Anna Rapisarda; Ariadna Bargiela; Beatriz Llamusi; Isabel Pont; Roger Estrada-Tejedor; Enrique Garcia-España; Ruben Artero; Manuel Perez-Alonso
Journal:  Sci Rep       Date:  2021-09-30       Impact factor: 4.379

  3 in total

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