A comparison of three different methods of eliciting rapid activity-dependent synaptic plasticity at the Drosophila NMJ.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2021
Historique:
received: 22 06 2021
accepted: 11 11 2021
entrez: 30 11 2021
pubmed: 1 12 2021
medline: 6 1 2022
Statut: epublish

Résumé

The Drosophila NMJ is a system of choice for investigating the mechanisms underlying the structural and functional modifications evoked during activity-dependent synaptic plasticity. Because fly genetics allows considerable versatility, many strategies can be employed to elicit this activity. Here, we compare three different stimulation methods for eliciting activity-dependent changes in structure and function at the Drosophila NMJ. We find that the method using patterned stimulations driven by a K+-rich solution creates robust structural modifications but reduces muscle viability, as assessed by resting potential and membrane resistance. We argue that, using this method, electrophysiological studies that consider the frequency of events, rather than their amplitude, are the only reliable studies. We contrast these results with the expression of CsChrimson channels and red-light stimulation at the NMJ, as well as with the expression of TRPA channels and temperature stimulation. With both these methods we observed reliable modifications of synaptic structures and consistent changes in electrophysiological properties. Indeed, we observed a rapid appearance of immature boutons that lack postsynaptic differentiation, and a potentiation of spontaneous neurotransmission frequency. Surprisingly, a patterned application of temperature changes alone is sufficient to provoke both structural and functional plasticity. In this context, temperature-dependent TRPA channel activation induces additional structural plasticity but no further increase in the frequency of spontaneous neurotransmission, suggesting an uncoupling of these mechanisms.

Identifiants

pubmed: 34847197
doi: 10.1371/journal.pone.0260553
pii: PONE-D-21-20520
pmc: PMC8631638
doi:

Substances chimiques

Drosophila Proteins 0
Transient Receptor Potential Channels 0

Types de publication

Comparative Study Journal Article Research Support, N.I.H., Extramural Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0260553

Subventions

Organisme : NIMHD NIH HHS
ID : U54 MD007600
Pays : United States
Organisme : NIGMS NIH HHS
ID : R25 GM061838
Pays : United States
Organisme : NIGMS NIH HHS
ID : P20 GM103642
Pays : United States
Organisme : NIMHD NIH HHS
ID : G12 MD007600
Pays : United States
Organisme : NINDS NIH HHS
ID : R21 NS114774
Pays : United States

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

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Auteurs

Carolina Maldonado-Díaz (C)

Institute of Neurobiology, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico.
Department of Anatomy & Neurobiology, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico.

Mariam Vazquez (M)

Institute of Neurobiology, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico.

Bruno Marie (B)

Institute of Neurobiology, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico.
Department of Anatomy & Neurobiology, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico.

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