Literature DB >> 22154366

Tubular aggregates in skeletal muscle: just a special type of protein aggregates?

Stefano Schiaffino1.   

Abstract

Tubular aggregates are inclusions, usually found in type II muscle fibers and in males, consisting of regular arrays of tubules derived from the sarcoplasmic reticulum. Tubular aggregates are associated with a wide variety of muscle disorders, including poorly defined "tubular aggregate myopathies" characterized by weakness and/or myalgia and/or cramps, and are also present in different mouse models, including normal aging muscles. The mechanism(s) responsible for inducing the formation of these structures have not been identified, because of the slow time course of their development in vivo, several months in mice. However, identical structures are formed in a few hours in rat muscles kept in vitro in hypoxic medium. Here I suggest that tubular aggregates result from reshaping of sarcoplasmic reticulum caused by misfolding and aggregation of membrane proteins and thus represent a special type of "protein aggregates" due to altered proteostasis.
Copyright © 2011 Elsevier B.V. All rights reserved.

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Year:  2011        PMID: 22154366     DOI: 10.1016/j.nmd.2011.10.005

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  34 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.  The RNA-binding protein Rbfox1 regulates splicing required for skeletal muscle structure and function.

Authors:  Simona Pedrotti; Jimena Giudice; Adan Dagnino-Acosta; Mark Knoblauch; Ravi K Singh; Amy Hanna; Qianxing Mo; John Hicks; Susan Hamilton; Thomas A Cooper
Journal:  Hum Mol Genet       Date:  2015-01-09       Impact factor: 6.150

Review 3.  Diseases caused by mutations in ORAI1 and STIM1.

Authors:  Rodrigo S Lacruz; Stefan Feske
Journal:  Ann N Y Acad Sci       Date:  2015-10-15       Impact factor: 5.691

Review 4.  Role of STIM1/ORAI1-mediated store-operated Ca2+ entry in skeletal muscle physiology and disease.

Authors:  Antonio Michelucci; Maricela García-Castañeda; Simona Boncompagni; Robert T Dirksen
Journal:  Cell Calcium       Date:  2018-10-30       Impact factor: 6.817

5.  Muscle injury, impaired muscle function and insulin resistance in Chromogranin A-knockout mice.

Authors:  Kechun Tang; Teresa Pasqua; Angshuman Biswas; Sumana Mahata; Jennifer Tang; Alisa Tang; Gautam K Bandyopadhyay; Amiya P Sinha-Hikim; Nai-Wen Chi; Nicholas J G Webster; Angelo Corti; Sushil K Mahata
Journal:  J Endocrinol       Date:  2016-10-31       Impact factor: 4.286

6.  Characterization of fast-twitch and slow-twitch skeletal muscles of calsequestrin 2 (CASQ2)-knock out mice: unexpected adaptive changes of fast-twitch muscles only.

Authors:  Giorgia Valle; Barbara Vergani; Roberta Sacchetto; Carlo Reggiani; Edith De Rosa; Lisa Maccatrozzo; Alessandra Nori; Antonello Villa; Pompeo Volpe
Journal:  J Muscle Res Cell Motil       Date:  2017-01-27       Impact factor: 2.698

7.  Brown Adipose Tissue Controls Skeletal Muscle Function via the Secretion of Myostatin.

Authors:  Xingxing Kong; Ting Yao; Peng Zhou; Lawrence Kazak; Danielle Tenen; Anna Lyubetskaya; Brian A Dawes; Linus Tsai; Barbara B Kahn; Bruce M Spiegelman; Tiemin Liu; Evan D Rosen
Journal:  Cell Metab       Date:  2018-08-02       Impact factor: 27.287

8.  Clinical features of congenital myasthenic syndrome due to mutations in DPAGT1.

Authors:  Sarah Finlayson; Jacqueline Palace; Katsiaryna Belaya; Timothy J Walls; Fiona Norwood; Georgina Burke; Janice L Holton; Samuel I Pascual-Pascual; Judith Cossins; David Beeson
Journal:  J Neurol Neurosurg Psychiatry       Date:  2013-02-27       Impact factor: 10.154

9.  Childhood onset tubular aggregate myopathy associated with de novo STIM1 mutations.

Authors:  Carola Hedberg; Marcello Niceta; Fabiana Fattori; Björn Lindvall; Andrea Ciolfi; Adele D'Amico; Giorgio Tasca; Stefania Petrini; Mar Tulinius; Marco Tartaglia; Anders Oldfors; Enrico Bertini
Journal:  J Neurol       Date:  2014-02-26       Impact factor: 4.849

10.  Constitutive activation of the calcium sensor STIM1 causes tubular-aggregate myopathy.

Authors:  Johann Böhm; Frédéric Chevessier; André Maues De Paula; Catherine Koch; Shahram Attarian; Claire Feger; Daniel Hantaï; Pascal Laforêt; Karima Ghorab; Jean-Michel Vallat; Michel Fardeau; Dominique Figarella-Branger; Jean Pouget; Norma B Romero; Marc Koch; Claudine Ebel; Nicolas Levy; Martin Krahn; Bruno Eymard; Marc Bartoli; Jocelyn Laporte
Journal:  Am J Hum Genet       Date:  2013-01-17       Impact factor: 11.025

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