Academic Journal

Branched actin polymerization drives invasive protrusion formation to promote myoblast fusion during mouse skeletal muscle regeneration

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Branched actin polymerization drives invasive protrusion formation to promote myoblast fusion during mouse skeletal muscle regeneration
Συγγραφείς: Lu, Yue, Walji, Tezin, Pandey, Pratima, Zhou, Chuanli, Habela, Christa W, Snapper, Scott B, Li, Rong, Chen, Elizabeth H
Συνεισφορές: American Heart Association, National Institute of General Medical Sciences
Πηγή: eLife ; volume 14 ; ISSN 2050-084X
Στοιχεία εκδότη: eLife Sciences Publications, Ltd
Έτος έκδοσης: 2026
Συλλογή: eLife (E-Journal - via CrossRef)
Περιγραφή: Skeletal muscle regeneration is a multistep process involving the activation, proliferation, differentiation, and fusion of muscle stem cells, known as satellite cells. Fusion of satellite cell-derived myoblasts (SCMs) is indispensable for generating the multinucleated, contractile myofibers during muscle repair. However, the molecular and cellular mechanisms underlying SCM fusion during muscle regeneration remain incompletely understood. Here, we reveal a critical role for branched actin polymerization in SCM fusion during mouse skeletal muscle regeneration. Using conditional knockouts of the Arp2/3 complex and its actin nucleation-promoting factors N-WASP and WAVE, we demonstrate that branched actin polymerization is specifically required for SCM fusion but dispensable for satellite cell proliferation, differentiation, and migration. We show that the N-WASP and WAVE complexes have partially redundant functions in regulating SCM fusion and that branched actin polymerization is essential for generating invasive protrusions at fusogenic synapses in SCMs. Together, our study identifies branched-actin regulators as key components of the myoblast fusion machinery and establishes invasive protrusion formation as a critical mechanism enabling myoblast fusion during skeletal muscle regeneration.
Τύπος εγγράφου: article in journal/newspaper
Γλώσσα: English
DOI: 10.7554/elife.103550
Διαθεσιμότητα: https://doi.org/10.7554/elife.103550
https://cdn.elifesciences.org/articles/103550/elife-103550-v1.pdf
https://cdn.elifesciences.org/articles/103550/elife-103550-v1.xml
https://elifesciences.org/articles/103550
Rights: http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/
Αριθμός Καταχώρησης: edsbas.6720B522
Βάση Δεδομένων: BASE
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  – Url: https://doi.org/10.7554/elife.103550#
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  Data: Branched actin polymerization drives invasive protrusion formation to promote myoblast fusion during mouse skeletal muscle regeneration
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  Data: <searchLink fieldCode="AR" term="%22Lu%2C+Yue%22">Lu, Yue</searchLink><br /><searchLink fieldCode="AR" term="%22Walji%2C+Tezin%22">Walji, Tezin</searchLink><br /><searchLink fieldCode="AR" term="%22Pandey%2C+Pratima%22">Pandey, Pratima</searchLink><br /><searchLink fieldCode="AR" term="%22Zhou%2C+Chuanli%22">Zhou, Chuanli</searchLink><br /><searchLink fieldCode="AR" term="%22Habela%2C+Christa+W%22">Habela, Christa W</searchLink><br /><searchLink fieldCode="AR" term="%22Snapper%2C+Scott+B%22">Snapper, Scott B</searchLink><br /><searchLink fieldCode="AR" term="%22Li%2C+Rong%22">Li, Rong</searchLink><br /><searchLink fieldCode="AR" term="%22Chen%2C+Elizabeth+H%22">Chen, Elizabeth H</searchLink>
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  Data: American Heart Association<br />National Institute of General Medical Sciences
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  Data: eLife ; volume 14 ; ISSN 2050-084X
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  Data: Skeletal muscle regeneration is a multistep process involving the activation, proliferation, differentiation, and fusion of muscle stem cells, known as satellite cells. Fusion of satellite cell-derived myoblasts (SCMs) is indispensable for generating the multinucleated, contractile myofibers during muscle repair. However, the molecular and cellular mechanisms underlying SCM fusion during muscle regeneration remain incompletely understood. Here, we reveal a critical role for branched actin polymerization in SCM fusion during mouse skeletal muscle regeneration. Using conditional knockouts of the Arp2/3 complex and its actin nucleation-promoting factors N-WASP and WAVE, we demonstrate that branched actin polymerization is specifically required for SCM fusion but dispensable for satellite cell proliferation, differentiation, and migration. We show that the N-WASP and WAVE complexes have partially redundant functions in regulating SCM fusion and that branched actin polymerization is essential for generating invasive protrusions at fusogenic synapses in SCMs. Together, our study identifies branched-actin regulators as key components of the myoblast fusion machinery and establishes invasive protrusion formation as a critical mechanism enabling myoblast fusion during skeletal muscle regeneration.
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  Data: 10.7554/elife.103550
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  Data: http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/ ; http://creativecommons.org/licenses/by/4.0/
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