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Ephrin-A3 promotes and maintains slow muscle fiber identity during postnatal development and reinnervation.


ABSTRACT: Each adult mammalian skeletal muscle has a unique complement of fast and slow myofibers, reflecting patterns established during development and reinforced via their innervation by fast and slow motor neurons. Existing data support a model of postnatal "matching" whereby predetermined myofiber type identity promotes pruning of inappropriate motor axons, but no molecular mechanism has yet been identified. We present evidence that fiber type-specific repulsive interactions inhibit innervation of slow myofibers by fast motor axons during both postnatal maturation of the neuromuscular junction and myofiber reinnervation after injury. The repulsive guidance ligand ephrin-A3 is expressed only on slow myofibers, whereas its candidate receptor, EphA8, localizes exclusively to fast motor endplates. Adult mice lacking ephrin-A3 have dramatically fewer slow myofibers in fast and mixed muscles, and misexpression of ephrin-A3 on fast myofibers followed by denervation/reinnervation promotes their respecification to a slow phenotype. We therefore conclude that Eph/ephrin interactions guide the fiber type specificity of neuromuscular interactions during development and adult life.

SUBMITTER: Stark DA 

PROVIDER: S-EPMC4674275 | biostudies-literature | 2015 Dec

REPOSITORIES: biostudies-literature

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Ephrin-A3 promotes and maintains slow muscle fiber identity during postnatal development and reinnervation.

Stark Danny A DA   Coffey Nathan J NJ   Pancoast Hannah R HR   Arnold Laura L LL   Walker J Peyton D JP   Vallée Joanne J   Robitaille Richard R   Garcia Michael L ML   Cornelison D D W DD  

The Journal of cell biology 20151201 5


Each adult mammalian skeletal muscle has a unique complement of fast and slow myofibers, reflecting patterns established during development and reinforced via their innervation by fast and slow motor neurons. Existing data support a model of postnatal "matching" whereby predetermined myofiber type identity promotes pruning of inappropriate motor axons, but no molecular mechanism has yet been identified. We present evidence that fiber type-specific repulsive interactions inhibit innervation of sl  ...[more]

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