Literature DB >> 27941137

Tubular Aggregates and Cylindrical Spirals Have Distinct Immunohistochemical Signatures.

Stefen Brady1, Estelle G Healy1, Qiang Gang1, Matt Parton1, Ros Quinlivan1, Saiju Jacob1, Elizabeth Curtis1, Safa Al-Sarraj1, Caroline A Sewry1, Michael G Hanna1, Henry Houlden1, David Beeson1, Janice L Holton2.   

Abstract

Tubular aggregates and cylindrical spirals are 2 distinct ultrastructural abnormalities observed in muscle biopsies that have similar histochemical staining characteristics on light microscopy. Both are found in a wide range of disorders. Recently, a number of genetic mutations have been reported in conditions with tubular aggregates in skeletal muscle. It is widely accepted that tubular aggregates arise from the sarcoplasmic reticulum, but the origin of cylindrical spirals has been less clearly defined. We describe the histopathological features of myopathies with tubular aggregates, including a detailed immunohistochemical analysis of congenital myasthenic syndromes with tubular aggregates due to mutations in GFPT1 and DPAGT1, and myopathies with cylindrical spirals. Our findings support the notion that cylindrical spirals, like tubular aggregates, derive primarily from the sarcoplasmic reticulum; however, immunohistochemistry indicates that different molecular components of the sarcoplasmic reticulum may be involved and can be used to distinguish between these different inclusions. The immunohistochemical differences may also help to guide genetic testing.
© 2016 American Association of Neuropathologists, Inc. All rights reserved.

Entities:  

Keywords:  Congenital myasthenic syndromes; Cylindrical spirals; Tubular aggregate myopathy.; Tubular aggregates

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Substances:

Year:  2016        PMID: 27941137     DOI: 10.1093/jnen/nlw096

Source DB:  PubMed          Journal:  J Neuropathol Exp Neurol        ISSN: 0022-3069            Impact factor:   3.685


  3 in total

1.  Mutations in GFPT1-related congenital myasthenic syndromes are associated with synaptic morphological defects and underlie a tubular aggregate myopathy with synaptopathy.

Authors:  Stéphanie Bauché; Geoffroy Vellieux; Damien Sternberg; Marie-Joséphine Fontenille; Elodie De Bruyckere; Claire-Sophie Davoine; Guy Brochier; Julien Messéant; Lucie Wolf; Michel Fardeau; Emmanuelle Lacène; Norma Romero; Jeanine Koenig; Emmanuel Fournier; Daniel Hantaï; Nathalie Streichenberger; Veronique Manel; Arnaud Lacour; Aleksandra Nadaj-Pakleza; Sylvie Sukno; Françoise Bouhour; Pascal Laforêt; Bertrand Fontaine; Laure Strochlic; Bruno Eymard; Frédéric Chevessier; Tanya Stojkovic; Sophie Nicole
Journal:  J Neurol       Date:  2017-07-15       Impact factor: 4.849

2.  Genetic defects are common in myopathies with tubular aggregates.

Authors:  Qiang Gang; Conceição Bettencourt; Stefen Brady; Janice L Holton; Estelle G Healy; John McConville; Patrick J Morrison; Michela Ripolone; Raffaella Violano; Monica Sciacco; Maurizio Moggio; Marina Mora; Renato Mantegazza; Simona Zanotti; Zhaoxia Wang; Yun Yuan; Wei-Wei Liu; David Beeson; Michael Hanna; Henry Houlden
Journal:  Ann Clin Transl Neurol       Date:  2021-12-15       Impact factor: 5.430

3.  Ryanodine receptor 1 (RYR1) mutations in two patients with tubular aggregate myopathy.

Authors:  Gaetano Nicola Alfio Vattemi; Daniela Rossi; Lucia Galli; Maria Rosaria Catallo; Elia Pancheri; Giulia Marchetto; Barbara Cisterna; Manuela Malatesta; Enrico Pierantozzi; Paola Tonin; Vincenzo Sorrentino
Journal:  Eur J Neurosci       Date:  2022-06-13       Impact factor: 3.698

  3 in total

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