Cargando…
Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission
Synapses maintain synchronous, asynchronous, and spontaneous modes of neurotransmission through distinct molecular and biochemical pathways. Traditionally a single synapse was assumed to have a homogeneous organization of molecular components both at the active zone and post-synaptically. However, r...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727373/ https://www.ncbi.nlm.nih.gov/pubmed/35002671 http://dx.doi.org/10.3389/fnsyn.2021.796498 |
_version_ | 1784626513057939456 |
---|---|
author | Guzikowski, Natalie J. Kavalali, Ege T. |
author_facet | Guzikowski, Natalie J. Kavalali, Ege T. |
author_sort | Guzikowski, Natalie J. |
collection | PubMed |
description | Synapses maintain synchronous, asynchronous, and spontaneous modes of neurotransmission through distinct molecular and biochemical pathways. Traditionally a single synapse was assumed to have a homogeneous organization of molecular components both at the active zone and post-synaptically. However, recent advancements in experimental tools and the further elucidation of the physiological significance of distinct forms of release have challenged this notion. In comparison to rapid evoked release, the physiological significance of both spontaneous and asynchronous neurotransmission has only recently been considered in parallel with synaptic structural organization. Active zone nanostructure aligns with postsynaptic nanostructure creating a precise trans-synaptic alignment of release sites and receptors shaping synaptic efficacy, determining neurotransmission reliability, and tuning plasticity. This review will discuss how studies delineating synaptic nanostructure create a picture of a molecularly heterogeneous active zone tuned to distinct forms of release that may dictate diverse synaptic functional outputs. |
format | Online Article Text |
id | pubmed-8727373 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87273732022-01-06 Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission Guzikowski, Natalie J. Kavalali, Ege T. Front Synaptic Neurosci Synaptic Neuroscience Synapses maintain synchronous, asynchronous, and spontaneous modes of neurotransmission through distinct molecular and biochemical pathways. Traditionally a single synapse was assumed to have a homogeneous organization of molecular components both at the active zone and post-synaptically. However, recent advancements in experimental tools and the further elucidation of the physiological significance of distinct forms of release have challenged this notion. In comparison to rapid evoked release, the physiological significance of both spontaneous and asynchronous neurotransmission has only recently been considered in parallel with synaptic structural organization. Active zone nanostructure aligns with postsynaptic nanostructure creating a precise trans-synaptic alignment of release sites and receptors shaping synaptic efficacy, determining neurotransmission reliability, and tuning plasticity. This review will discuss how studies delineating synaptic nanostructure create a picture of a molecularly heterogeneous active zone tuned to distinct forms of release that may dictate diverse synaptic functional outputs. Frontiers Media S.A. 2021-12-22 /pmc/articles/PMC8727373/ /pubmed/35002671 http://dx.doi.org/10.3389/fnsyn.2021.796498 Text en Copyright © 2021 Guzikowski and Kavalali. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Synaptic Neuroscience Guzikowski, Natalie J. Kavalali, Ege T. Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission |
title | Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission |
title_full | Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission |
title_fullStr | Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission |
title_full_unstemmed | Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission |
title_short | Nano-Organization at the Synapse: Segregation of Distinct Forms of Neurotransmission |
title_sort | nano-organization at the synapse: segregation of distinct forms of neurotransmission |
topic | Synaptic Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727373/ https://www.ncbi.nlm.nih.gov/pubmed/35002671 http://dx.doi.org/10.3389/fnsyn.2021.796498 |
work_keys_str_mv | AT guzikowskinataliej nanoorganizationatthesynapsesegregationofdistinctformsofneurotransmission AT kavalalieget nanoorganizationatthesynapsesegregationofdistinctformsofneurotransmission |