Literature DB >> 15086789

Membrane traffic in skeletal muscle.

Mhairi C Towler1, Stephen J Kaufman, Frances M Brodsky.   

Abstract

Skeletal muscle tissue is made up of highly organized multinuclear cells. The internal organization of the muscle cell is dictated by the necessary regular arrangement of repeated units within the protein myofibrils that mediate muscle contraction. Skeletal muscle cells have the usual membrane traffic pathways for partitioning newly synthesized proteins, internalizing cell surface receptors for hormones and nutrients, and mediating membrane repair. However, in muscle, these pathways must be further specialized to deal with targeting to and organizing muscle-specific membrane structures, satisfying the unique metabolic requirements of muscle and meeting the high demand for membrane repair in a tissue that is constantly under mechanical stress. Specialized membrane traffic pathways in muscle also play a role in the formation of muscle through fusion of myoblast membranes and the development of internal muscle-specific membrane structures during myogenesis and regeneration. It has recently become apparent that muscle-specific isoforms of proteins that are known to mediate ubiquitous membrane traffic pathways, as well as novel muscle-specific proteins, are involved in tissue-specific aspects of muscle membrane traffic. Here we describe the specialized membrane structures of skeletal muscle, how these are developed, maintained and repaired by specialized and generic membrane traffic pathways, and how defects in these pathways result in muscle disease.

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Year:  2004        PMID: 15086789     DOI: 10.1111/j.1600-0854.2003.00164.x

Source DB:  PubMed          Journal:  Traffic        ISSN: 1398-9219            Impact factor:   6.215


  23 in total

Review 1.  Non-canonical roles for caveolin in regulation of membrane repair and mitochondria: implications for stress adaptation with age.

Authors:  Jan M Schilling; Hemal H Patel
Journal:  J Physiol       Date:  2015-10-14       Impact factor: 5.182

2.  Vesicular transport system in myotubes: ultrastructural study and signposting with vesicle-associated membrane proteins.

Authors:  Yuki Tajika; Maiko Takahashi; Astrid Feinisa Khairani; Hitoshi Ueno; Tohru Murakami; Hiroshi Yorifuji
Journal:  Histochem Cell Biol       Date:  2013-11-22       Impact factor: 4.304

3.  Obstructed metabolite diffusion within skeletal muscle cells in silico.

Authors:  Mayis K Aliev; Alexander N Tikhonov
Journal:  Mol Cell Biochem       Date:  2011-06-28       Impact factor: 3.396

4.  Amphiphysin (BIN1) negatively regulates dynamin 2 for normal muscle maturation.

Authors:  Belinda S Cowling; Ivana Prokic; Hichem Tasfaout; Aymen Rabai; Frédéric Humbert; Bruno Rinaldi; Anne-Sophie Nicot; Christine Kretz; Sylvie Friant; Aurélien Roux; Jocelyn Laporte
Journal:  J Clin Invest       Date:  2017-11-13       Impact factor: 14.808

5.  Zinc Binding to MG53 Protein Facilitates Repair of Injury to Cell Membranes.

Authors:  Chuanxi Cai; Peihui Lin; Hua Zhu; Jae-Kyun Ko; Moonsun Hwang; Tao Tan; Zui Pan; Irina Korichneva; Jianjie Ma
Journal:  J Biol Chem       Date:  2015-04-13       Impact factor: 5.157

6.  VAMP2 marks quiescent satellite cells and myotubes, but not activated myoblasts.

Authors:  Yuki Tajika; Maiko Takahashi; Mizuki Hino; Tohru Murakami; Hiroshi Yorifuji
Journal:  Acta Histochem Cytochem       Date:  2010-08-03       Impact factor: 1.938

7.  MG53 nucleates assembly of cell membrane repair machinery.

Authors:  Chuanxi Cai; Haruko Masumiya; Noah Weisleder; Noriyuki Matsuda; Miyuki Nishi; Moonsun Hwang; Jae-Kyun Ko; Peihui Lin; Angela Thornton; Xiaoli Zhao; Zui Pan; Shinji Komazaki; Marco Brotto; Hiroshi Takeshima; Jianjie Ma
Journal:  Nat Cell Biol       Date:  2008-11-30       Impact factor: 28.824

8.  Membrane repair defects in muscular dystrophy are linked to altered interaction between MG53, caveolin-3, and dysferlin.

Authors:  Chuanxi Cai; Noah Weisleder; Jae-Kyun Ko; Shinji Komazaki; Yoshihide Sunada; Miyuki Nishi; Hiroshi Takeshima; Jianjie Ma
Journal:  J Biol Chem       Date:  2009-04-20       Impact factor: 5.157

9.  Clathrin isoform CHC22, a component of neuromuscular and myotendinous junctions, binds sorting nexin 5 and has increased expression during myogenesis and muscle regeneration.

Authors:  Mhairi C Towler; Paul A Gleeson; Sachiko Hoshino; Paavo Rahkila; Venus Manalo; Norio Ohkoshi; Charles Ordahl; Robert G Parton; Frances M Brodsky
Journal:  Mol Biol Cell       Date:  2004-05-07       Impact factor: 4.138

10.  Functional equivalence of the clathrin heavy chains CHC17 and CHC22 in endocytosis and mitosis.

Authors:  Fiona E Hood; Stephen J Royle
Journal:  J Cell Sci       Date:  2009-06-09       Impact factor: 5.285

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