» Articles » PMID: 21206479

Paraffin-embedded and Frozen Sections of Drosophila Adult Muscles

Overview
Journal J Vis Exp
Date 2011 Jan 6
PMID 21206479
Citations 21
Authors
Affiliations
Soon will be listed here.
Abstract

The molecular characterization of muscular dystrophies and myopathies in humans has revealed the complexity of muscle disease and genetic analysis of muscle specification, formation and function in model systems has provided valuable insight into muscle physiology. Therefore, identifying and characterizing molecular mechanisms that underlie muscle damage is critical. The structure of adult Drosophila multi-fiber muscles resemble vertebrate striated muscles (1) and the genetic tractability of Drosophila has made it a great system to analyze dystrophic muscle morphology and characterize the processes affecting muscular function in ageing adult flies (2). Here we present the histological technique for preparing paraffin-embedded and frozen sections of Drosophila thoracic muscles. These preparations allow for the tissue to be stained with classical histological stains and labeled with protein detecting dyes, and specifically cryosections are ideal for immunohistochemical detection of proteins in intact muscles. This allows for analysis of muscle tissue structure, identification of morphological defects, and detection of the expression pattern for muscle/neuron-specific proteins in Drosophila adult muscles. These techniques can also be slightly modified for sectioning of other body parts.

Citing Articles

mir-276a Is Required for Muscle Development in and Regulates the FGF Receptor During the Migration of Nascent Myotubes in the Testis.

Preussner M, Bischoff M, Onel S Cells. 2025; 14(5).

PMID: 40072096 PMC: 11898445. DOI: 10.3390/cells14050368.


Mitigation of TDP-43 toxic phenotype by an RGNEF fragment in amyotrophic lateral sclerosis models.

Droppelmann C, Campos-Melo D, Noches V, McLellan C, Szabla R, Lyons T Brain. 2024; 147(6):2053-2068.

PMID: 38739752 PMC: 11146434. DOI: 10.1093/brain/awae078.


Unraveling the link between neuropathy target esterase NTE/SWS, lysosomal storage diseases, inflammation, abnormal fatty acid metabolism, and leaky brain barrier.

Tsap M, Yatsenko A, Hegermann J, Beckmann B, Tsikas D, Shcherbata H Elife. 2024; 13.

PMID: 38660940 PMC: 11090517. DOI: 10.7554/eLife.98020.


Reducing the Excess Activin Signaling Rescues Muscle Degeneration in Myotonic Dystrophy Type 2 Model.

Deng J, Guan X, Zhu Y, Deng H, Li G, Guo Y J Pers Med. 2022; 12(3).

PMID: 35330385 PMC: 8948895. DOI: 10.3390/jpm12030385.


Tissue-specific regulation of translational readthrough tunes functions of the traffic jam transcription factor.

Karki P, Carney T, Maracci C, Yatsenko A, Shcherbata H, Rodnina M Nucleic Acids Res. 2021; 50(11):6001-6019.

PMID: 34897510 PMC: 9226519. DOI: 10.1093/nar/gkab1189.


References
1.
Shcherbata H, Yatsenko A, Patterson L, Sood V, Nudel U, Yaffe D . Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy. EMBO J. 2007; 26(2):481-93. PMC: 1783456. DOI: 10.1038/sj.emboj.7601503. View

2.
Kucherenko M, Pantoja M, Yatsenko A, Shcherbata H, Fischer K, Maksymiv D . Genetic modifier screens reveal new components that interact with the Drosophila dystroglycan-dystrophin complex. PLoS One. 2008; 3(6):e2418. PMC: 2398783. DOI: 10.1371/journal.pone.0002418. View

3.
Sieber M, Thummel C . The DHR96 nuclear receptor controls triacylglycerol homeostasis in Drosophila. Cell Metab. 2009; 10(6):481-90. PMC: 2803078. DOI: 10.1016/j.cmet.2009.10.010. View

4.
PUCHTLER H, Waldrop F, Conner H, Terry M . Carnoy fixation: practical and theoretical considerations. Histochemie. 1968; 16(4):361-71. DOI: 10.1007/BF00306359. View