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Early postsynaptic instability and acetylcholine receptor compartmentalization precede neuromuscular synapse dismantling
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  • Published: 11 March 2026

Early postsynaptic instability and acetylcholine receptor compartmentalization precede neuromuscular synapse dismantling

  • Diego Zelada1,2 nAff4,
  • Francisca Bermedo-García  ORCID: orcid.org/0000-0001-9240-51841,
  • Jessica Mella1,
  • Hugo C. Olguín3 &
  • …
  • Juan Pablo Henríquez  ORCID: orcid.org/0000-0003-0820-73591,2 

Communications Biology , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Cellular neuroscience
  • Regeneration and repair in the nervous system

Abstract

The neuromuscular junction (NMJ) is the peripheral synapse controlling muscle contraction. Although aging and neurodegeneration result in NMJ denervation and synaptic dismantling, early indicators of this process remain elusive. Here, we analyzed the organization and dynamics of postsynaptic nicotinic acetylcholine receptors (nAChR) following muscle denervation. Using fluorescent conjugates of α-bungarotoxin (BTX), we found that loss of nAChR stability preceded morphological disintegration. Early after denervation, the combined use of receptor labeling and lectin staining revealed a rearrangement of long-lasting or newly inserted receptors that resulted in a novel compartmentalized postsynaptic pattern in which stable, pre-existing nAChRs concentrated centrally, while newly inserted, dynamic receptors localized peripherally. Small ectopic, highly dynamic nAChR clusters emerged since early denervation. Additionally, intracellular ring-like nAChR aggregates emerged since early denervation stages and were distributed in perinuclear regions, co-localizing with the lysosomal marker LAMP1, consistent with a degradative fate. Altogether, specific combinations of nAChR dynamics and morphologies serve as early markers of NMJ dismantling. These novel criteria to assess NMJ integrity may help define therapeutic windows to promote reinnervation in degenerative neuromuscular conditions.

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Data availability

All data generated or analyzed during this study are included in this published article and its supplementary information files (Supplementary Data 1).

Code availability

No custom code was used in this study. Analyses were performed using standard software as described in the “Methods” section.

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Acknowledgements

We thank the highly collaborative and stimulating environment of the NeSt Lab members for their useful discussion and comments on this work. Our research has been supported by research grants FONDECYT 1170614, 1221213 to JPH and 3240731 to JM, AFM-Telethon 24878, and FONDECYT 1241240 to HO. DZ, FB-G, and JM have been ANID fellows.

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  1. Diego Zelada

    Present address: Department of Anatomy and Cell Biology, College of Medicine, University of Illinois at Chicago, Chicago, IL, USA

Authors and Affiliations

  1. Neuromuscular Studies Lab (NeSt Lab), Instituto de Anatomía, Histología y Patología, Facultad de Medicina, Universidad Austral de Chile, Valdivia, Chile

    Diego Zelada, Francisca Bermedo-García, Jessica Mella & Juan Pablo Henríquez

  2. Departamento de Biología Celular, Facultad de Ciencias Biológicas, Universidad de Concepción, Concepción, Chile

    Diego Zelada & Juan Pablo Henríquez

  3. Laboratory of Tissue Repair and Adult Stem Cells, Molecular and Cell Biology Department, Faculty of Biological Sciences, P. Universidad Católica de Chile, Santiago, Chile

    Hugo C. Olguín

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Contributions

D.Z. designed the work, performed experiments and quantifications, analyzed, and interpreted data, and was a major contributor in writing the manuscript. F.B.-G. performed experiments, quantifications, and contributed to writing the manuscript. J.M. performed quantifications. H.O. assisted with experiments and contributed to writing the manuscript. J.P.H. designed the work, analyzed, and interpreted data, and was a major contributor in writing the manuscript. All authors read and approved the final manuscript.

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Correspondence to Juan Pablo Henríquez.

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Communications Biology thanks Mohammed Akaaboune and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Primary Handling Editors: Ivo Lieberam and Benjamin Bessieres. A peer review file is available.

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Zelada, D., Bermedo-García, F., Mella, J. et al. Early postsynaptic instability and acetylcholine receptor compartmentalization precede neuromuscular synapse dismantling. Commun Biol (2026). https://doi.org/10.1038/s42003-026-09816-3

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  • Received: 25 May 2025

  • Accepted: 24 February 2026

  • Published: 11 March 2026

  • DOI: https://doi.org/10.1038/s42003-026-09816-3

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