» Articles » PMID: 3892537

Neural Cell Adhesion Molecule (N-CAM) Accumulates in Denervated and Paralyzed Skeletal Muscles

Overview
Specialty Science
Date 1985 Jul 1
PMID 3892537
Citations 92
Authors
Affiliations
Soon will be listed here.
Abstract

We have used immunofluorescence and immunoblotting methods to study the amount and distribution of the neural cell adhesion molecule (N-CAM) in rat skeletal muscle; this molecule is thought to mediate adhesion of neurons to cultured myotubes. N-CAM is present on the surface of embryonic myotubes, but it is lost as development proceeds and is nearly absent from adult muscle. However, denervation of adult muscle results in the reappearance of N-CAM. In denervated muscle, N-CAM is associated both with muscle fibers and with cells in interstitial spaces between fibers. The N-CAM in interstitial spaces is concentrated near denervated endplates, which are known to be preferential sites for reinnervation. Paralysis of innervated muscle, known to mimic denervation in many respects, also induces the accumulation of N-CAM. Axons that regenerate to reinnervate muscle bear N-CAM on their terminals, and reinnervation results in the disappearance of N-CAM from muscle. Denervation induces accumulation of N-CAM in mouse and chicken, as well as in rat muscles. Thus, the expression of N-CAM in muscle is regulated by the muscle's state of innervation. In that N-CAM-rich muscles (embryonic, denervated, and paralyzed) are known to be competent to accept synapses, while N-CAM-poor muscles (normal adult and reinnervated) are refractory to hyperinnervation, N-CAM might, in turn, participate in regulating muscle's susceptibility to innervation.

Citing Articles

Single-nuclei sequencing of skeletal muscle reveals subsynaptic-specific transcripts involved in neuromuscular junction maintenance.

Ham A, Lin S, Tse A, Thurkauf M, McGowan T, Jorin L Nat Commun. 2025; 16(1):2220.

PMID: 40044687 PMC: 11882927. DOI: 10.1038/s41467-025-57487-1.


Neuromuscular impairment at different stages of human sarcopenia.

Sarto F, Franchi M, McPhee J, Stashuk D, Paganini M, Monti E J Cachexia Sarcopenia Muscle. 2024; 15(5):1797-1810.

PMID: 39236304 PMC: 11446718. DOI: 10.1002/jcsm.13531.


A molecular pathway for cancer cachexia-induced muscle atrophy revealed at single-nucleus resolution.

Zhang Y, Dos Santos M, Huang H, Chen K, Iyengar P, Infante R Cell Rep. 2024; 43(8):114587.

PMID: 39116208 PMC: 11472345. DOI: 10.1016/j.celrep.2024.114587.


Accelerated sarcopenia precedes learning and memory impairments in the P301S mouse model of tauopathies and Alzheimer's disease.

Longo S, Messi M, Wang Z, Meeker W, Delbono O J Cachexia Sarcopenia Muscle. 2024; 15(4):1358-1375.

PMID: 38646816 PMC: 11294019. DOI: 10.1002/jcsm.13482.


Imaging mass cytometry analysis of Becker muscular dystrophy muscle samples reveals different stages of muscle degeneration.

Pinol-Jurado P, Verdu-Diaz J, Fernandez-Simon E, Dominguez-Gonzalez C, Hernandez-Lain A, Lawless C Sci Rep. 2024; 14(1):3365.

PMID: 38336890 PMC: 10858026. DOI: 10.1038/s41598-024-51906-x.


References
1.
Sanes J, Marshall L, McMahan U . Reinnervation of muscle fiber basal lamina after removal of myofibers. Differentiation of regenerating axons at original synaptic sites. J Cell Biol. 1978; 78(1):176-98. PMC: 2110176. DOI: 10.1083/jcb.78.1.176. View

2.
Korneliussen H, Sommerschild H . Ultrastructure of the new neuromuscular junctions formed during reinnervation of rat soleus muscle by a "foreign" nerve. Cell Tissue Res. 1976; 167(4):439-52. DOI: 10.1007/BF00215176. View

3.
Fambrough D . Control of acetylcholine receptors in skeletal muscle. Physiol Rev. 1979; 59(1):165-227. DOI: 10.1152/physrev.1979.59.1.165. View

4.
Sanes J . More nerve growth factors?. Nature. 1984; 307(5951):500. DOI: 10.1038/307500a0. View

5.
Laemmli U . Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature. 1970; 227(5259):680-5. DOI: 10.1038/227680a0. View