Literature DB >> 35367215

Regulation of the myoblast fusion reaction for muscle development, regeneration, and adaptations.

Douglas P Millay1.   

Abstract

Fusion of plasma membranes is essential for skeletal muscle development, regeneration, exercise-induced adaptations, and results in a cell that contains hundreds to thousands of nuclei within a shared cytoplasm. The differentiation process in myocytes culminates in their fusion to form a new myofiber or fusion to an existing myofiber thereby contributing more synthetic material to the syncytium. The choice for two cells to fuse and become one could be a dangerous event if the two cells are not committed to an allied function. Thus, fusion events are highly regulated with positive and negative factors to fine-tune the process, and requires muscle-specific fusogens (Myomaker and Myomerger) as well as general cellular machinery to achieve the union of membranes. While a unified vertebrate myoblast fusion pathway is not yet established, recent discoveries should make this pursuit attainable. Not only does myocyte fusion impact the normal biology of skeletal muscle, but new evidence indicates dysregulation of the process impacts pathologies of skeletal muscle. Here, I will highlight the molecular players and biochemical mechanisms that drive fusion events in muscle, and discuss how this key myogenic process impacts skeletal muscle diseases.
Copyright © 2022 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Muscle development; Myoblast fusion; Myomaker; Myomerger; Myomixer; Regeneration

Mesh:

Substances:

Year:  2022        PMID: 35367215      PMCID: PMC9058940          DOI: 10.1016/j.yexcr.2022.113134

Source DB:  PubMed          Journal:  Exp Cell Res        ISSN: 0014-4827            Impact factor:   4.145


  91 in total

1.  Myomaker and Myomerger Work Independently to Control Distinct Steps of Membrane Remodeling during Myoblast Fusion.

Authors:  Evgenia Leikina; Dilani G Gamage; Vikram Prasad; Joanna Goykhberg; Michael Crowe; Jiajie Diao; Michael M Kozlov; Leonid V Chernomordik; Douglas P Millay
Journal:  Dev Cell       Date:  2018-09-06       Impact factor: 12.270

2.  Carey-Fineman-Ziter Syndrome: A MYMK-Related Myopathy Mimicking Brainstem Dysgenesis.

Authors:  Ana Camacho; Beatriz Martínez; Sara Alvarez; Belén Gil-Fournier; Soraya Ramiro; Aurelio Hernández-Laín; Noemí Núñez; Rogelio Simón
Journal:  J Neuromuscul Dis       Date:  2020

3.  Control of muscle formation by the fusogenic micropeptide myomixer.

Authors:  Pengpeng Bi; Andres Ramirez-Martinez; Hui Li; Jessica Cannavino; John R McAnally; John M Shelton; Efrain Sánchez-Ortiz; Rhonda Bassel-Duby; Eric N Olson
Journal:  Science       Date:  2017-04-06       Impact factor: 47.728

Review 4.  Invasive podosomes and myoblast fusion.

Authors:  Elizabeth H Chen
Journal:  Curr Top Membr       Date:  2011       Impact factor: 3.049

5.  The atypical Rac activator Dock180 (Dock1) regulates myoblast fusion in vivo.

Authors:  Mélanie Laurin; Nadine Fradet; Anne Blangy; Alan Hall; Kristiina Vuori; Jean-François Côté
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-26       Impact factor: 11.205

6.  GRAF1 promotes ferlin-dependent myoblast fusion.

Authors:  Kaitlin C Lenhart; Abby L Becherer; Jianbin Li; Xiao Xiao; Elizabeth M McNally; Christopher P Mack; Joan M Taylor
Journal:  Dev Biol       Date:  2014-07-11       Impact factor: 3.582

Review 7.  Acting on identity: Myoblast fusion and the formation of the syncytial muscle fiber.

Authors:  Su Deng; Mafalda Azevedo; Mary Baylies
Journal:  Semin Cell Dev Biol       Date:  2017-11-06       Impact factor: 7.727

8.  Myomaker is essential for muscle regeneration.

Authors:  Douglas P Millay; Lillian B Sutherland; Rhonda Bassel-Duby; Eric N Olson
Journal:  Genes Dev       Date:  2014-08-01       Impact factor: 11.361

Review 9.  Myoblast fusion confusion: the resolution begins.

Authors:  Srihari C Sampath; Srinath C Sampath; Douglas P Millay
Journal:  Skelet Muscle       Date:  2018-01-31       Impact factor: 4.912

10.  Spatiotemporal regulation of the GPCR activity of BAI3 by C1qL4 and Stabilin-2 controls myoblast fusion.

Authors:  Noumeira Hamoud; Viviane Tran; Takahiro Aimi; Wataru Kakegawa; Sylvie Lahaie; Marie-Pier Thibault; Ariane Pelletier; G William Wong; In-San Kim; Artur Kania; Michisuke Yuzaki; Michel Bouvier; Jean-François Côté
Journal:  Nat Commun       Date:  2018-10-26       Impact factor: 14.919

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