Evidence map›Paper›PMID 27656017›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Schwann Cells in Neuromuscular Junction Formation and Maintenance.

Arnab Barik, Lei Li, Anupama Sathyamurthy, Wen-Cheng Xiong, Lin Mei

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

67 citing papers in PubMed.

  1. Article
  2. A who's who of cell types in skeletal muscle.Communications biology · 2026
    Review
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  7. Review
  8. Article
  9. Reactive oxygen species in the pathogenesis of sarcopenia.Free radical biology & medicine · 2025
    Review
  10. Article
  11. Article
  12. The MuSK agonist antibody protects the neuromuscular junction and extends the lifespan in C9orf72-ALS mice.Molecular therapy : the journal of the American Society of Gene Therapy · 2024
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. The emergence of the stem cell niche.Trends in cell biology · 2023
    Review

7 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Arnab BarikDepartment of Neuroscience and Regenerative Medicine and.ORCID 0000-0001-6850-0894
Lei LiDepartment of Neuroscience and Regenerative Medicine and.ORCID 0000-0003-0480-6610
Anupama SathyamurthyDepartment of Neuroscience and Regenerative Medicine and.ORCID 0000-0001-9731-3043
Wen-Cheng XiongDepartment of Neuroscience and Regenerative Medicine and Department of Neurology, Medical College of Georgia, Augusta University, Augusta, Georgia 30912, and Charlie Norwood Veterans Administration Medical Center, Augusta, Georgia 30904.ORCID 0000-0001-9071-7598
Lin MeiDepartment of Neuroscience and Regenerative Medicine and Department of Neurology, Medical College of Georgia, Augusta University, Augusta, Georgia 30912, and Charlie Norwood Veterans Administration Medical Center, Augusta, Georgia 30904 lmei@augusta.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

unlabelledThe neuromuscular junction (NMJ) is a tripartite synapse that is formed by motor nerve terminals, postjunctional muscle membranes, and terminal Schwann cells (TSCs) that cover the nerve-muscle contact. NMJ formation requires intimate communications among the three different components. Unlike nerve-muscle interaction, which has been well characterized, less is known about the role of SCs in NMJ formation and maintenance. We show that SCs in mice lead nerve terminals to prepatterned AChRs. Ablating SCs at E8.5 (i.e., prior nerve arrival at the clusters) had little effect on aneural AChR clusters at E13.5, suggesting that SCs may not be necessary for aneural clusters. SC ablation at E12.5, a time when phrenic nerves approach muscle fibers, resulted in smaller and fewer nerve-induced AChR clusters; however, SC ablation at E15.5 reduced AChR cluster size but had no effect on cluster density, suggesting that SCs are involved in AChR cluster maturation. Miniature endplate potential amplitude, but not frequency, was reduced when SCs were ablated at E15.5, suggesting that postsynaptic alterations may occur ahead of presynaptic deficits. Finally, ablation of SCs at P30, after NMJ maturation, led to NMJ fragmentation and neuromuscular transmission deficits. Miniature endplate potential amplitude was reduced 3 d after SC ablation, but both amplitude and frequency were reduced 6 d after. Together, these results indicate that SCs are not only required for NMJ formation, but also necessary for its maintenance; and postsynaptic function and structure appeared to be more sensitive to SC ablation. SIGNIFICANCE STATEMENT: Neuromuscular junctions (NMJs) are critical for survival and daily functioning. Defects in NMJ formation during development or maintenance in adulthood result in debilitating neuromuscular disorders. The role of Schwann cells (SCs) in NMJ formation and maintenance was not well understood. We genetically ablated SCs during development and after NMJ formation to investigate the consequences of the ablation. This study reveals a critical role of SCs in NMJ formation as well as maintenance.

Indexed as

Action PotentialsAnimalsAnimals, NewbornBungarotoxinsElectromyographyEmbryo, MammalianEstrogen AntagonistsGreen Fluorescent ProteinsHomeodomain ProteinsMiceMice, TransgenicMyelin Proteolipid ProteinNeurofilament ProteinsNeuromuscular JunctionProteinsReceptors, CholinergicBungarotoxinsEstrogen AntagonistsGreen Fluorescent ProteinsHb9 protein, mouseHomeodomain ProteinsMyelin Proteolipid Proteinneurofilament protein HNeurofilament ProteinsPlp1 protein, mouseProteinsReceptors, Cholinergicrhodamine-alpha-bungarotoxinRhodaminesROSA22 protein, mouseS100 Calcium Binding Protein beta SubunitSynaptophysinTamoxifenTranscription FactorsAChRsgliaNMJSchwann cell

Identifiers

PMID27656017
PMCPMC5030347

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.