Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

GAP43 identifies developing muscle cells in human embryos

T Moos1, L R Christensen

  • 1Department of Medical Anatomy, Panum Institute, University of Copenhagen, Denmark.

Neuroreport
|September 30, 1993
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Accessing targeted nanoparticles to the brain: the vascular route.

Current medicinal chemistry·2014
Same author

Uptake and transport of superparamagnetic iron oxide nanoparticles through human brain capillary endothelial cells.

ACS chemical neuroscience·2013
Same author

Nanoparticle-derived non-viral genetic transfection at the blood-brain barrier to enable neuronal growth factor delivery by secretion from brain endothelium.

Current medicinal chemistry·2011
Same author

Developmental iron uptake and axonal transport in the retina of the rat.

Molecular and cellular neurosciences·2011
Same author

STREPTOCOCCAL FIBRINOLYSIS: A PROTEOLYTIC REACTION DUE TO A SERUM ENZYME ACTIVATED BY STREPTOCOCCAL FIBRINOLYSIN.

The Journal of general physiology·2009
Same author

A PROTEOLYTIC ENZYME OF SERUM: CHARACTERIZATION, ACTIVATION, AND REACTION WITH INHIBITORS.

The Journal of general physiology·2009
Same journal

Electroacupuncture alleviates neuroinflammation and promotes recovery of neurological functions after intracerebral hemorrhage by modulating α7nAChR/JAK2/STAT3 signaling pathway.

Neuroreport·2026
Same journal

Non-cell-autonomous regulation of Bhlhb5 expression in cortical projection neurons by GABAergic interneuron development and position.

Neuroreport·2026
Same journal

C-C motif chemokine ligand 3 mediates inflammatory response via NLRP3 inflammasome and neuron damage after traumatic brain injury.

Neuroreport·2026
Same journal

Methyltransferase-like 14 alleviates neuronal ferroptosis in Alzheimer's disease by regulating the peroxiredoxin 6/apoptosis signal-regulating kinase 1 signaling pathway.

Neuroreport·2026
Same journal

Hand mental rotation reaction time reflects motor imagery strategy and predicts changes in finger dexterity after motor imagery.

Neuroreport·2026
Same journal

Functional exploration of metabotropic glycine receptors in cultured rat hippocampal slices.

Neuroreport·2026
See all related articles

Growth associated protein 43 (GAP43) is newly found in developing human muscle cells. This protein, previously thought to be neuron-specific, is present in aneural embryonic muscle, expanding its known biological roles.

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Muscle Physiology

Background:

  • Growth associated protein 43 (GAP43) is traditionally recognized as a neuron-specific intracellular molecule.
  • Its presence is well-documented in the central and peripheral nervous systems, particularly during development and regeneration.
  • Recent findings indicated GAP43 expression in developing chicken muscle cells, challenging its neuron-exclusive status.

Purpose of the Study:

  • To investigate the expression of GAP43 in developing human muscle cells.
  • To determine if GAP43's role extends beyond neuronal tissues into myogenic development.
  • To confirm the presence of GAP43 in human embryonic muscle using specific cellular markers.

Main Methods:

  • Immunohistochemistry was employed to detect GAP43 protein localization.

Related Experiment Videos

  • Specific monoclonal antibodies were used to identify developing muscle cells (desmin) and axon terminals (synaptophysin).
  • Analysis focused on human embryonic muscle tissue samples.
  • Main Results:

    • GAP43 was detected in human embryonic muscle cells.
    • The expression of GAP43 was observed in muscle cells that were aneural (lacking nerve connections).
    • Results confirmed GAP43 presence in developing human muscle tissue.

    Conclusions:

    • GAP43 is expressed in developing human muscle cells.
    • This finding suggests a broader role for GAP43 in cellular development beyond the nervous system.
    • The presence of GAP43 in aneural muscle cells opens new avenues for understanding muscle development and regeneration.