Cargando…
Spontaneous Activity Predicts Survival of Developing Cortical Neurons
Spontaneous activity plays a crucial role in brain development by coordinating the integration of immature neurons into emerging cortical networks. High levels and complex patterns of spontaneous activity are generally associated with low rates of apoptosis in the cortex. However, whether spontaneou...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399774/ https://www.ncbi.nlm.nih.gov/pubmed/36035995 http://dx.doi.org/10.3389/fcell.2022.937761 |
_version_ | 1784772601885753344 |
---|---|
author | Warm, Davide Bassetti, Davide Schroer, Jonas Luhmann, Heiko J. Sinning, Anne |
author_facet | Warm, Davide Bassetti, Davide Schroer, Jonas Luhmann, Heiko J. Sinning, Anne |
author_sort | Warm, Davide |
collection | PubMed |
description | Spontaneous activity plays a crucial role in brain development by coordinating the integration of immature neurons into emerging cortical networks. High levels and complex patterns of spontaneous activity are generally associated with low rates of apoptosis in the cortex. However, whether spontaneous activity patterns directly encode for survival of individual cortical neurons during development remains an open question. Here, we longitudinally investigated spontaneous activity and apoptosis in developing cortical cultures, combining extracellular electrophysiology with calcium imaging. These experiments demonstrated that the early occurrence of calcium transients was strongly linked to neuronal survival. Silent neurons exhibited a higher probability of cell death, whereas high frequency spiking and burst behavior were almost exclusively detected in surviving neurons. In local neuronal clusters, activity of neighboring neurons exerted a pro-survival effect, whereas on the functional level, networks with a high modular topology were associated with lower cell death rates. Using machine learning algorithms, cell fate of individual neurons was predictable through the integration of spontaneous activity features. Our results indicate that high frequency spiking activity constrains apoptosis in single neurons through sustained calcium rises and thereby consolidates networks in which a high modular topology is reached during early development. |
format | Online Article Text |
id | pubmed-9399774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-93997742022-08-25 Spontaneous Activity Predicts Survival of Developing Cortical Neurons Warm, Davide Bassetti, Davide Schroer, Jonas Luhmann, Heiko J. Sinning, Anne Front Cell Dev Biol Cell and Developmental Biology Spontaneous activity plays a crucial role in brain development by coordinating the integration of immature neurons into emerging cortical networks. High levels and complex patterns of spontaneous activity are generally associated with low rates of apoptosis in the cortex. However, whether spontaneous activity patterns directly encode for survival of individual cortical neurons during development remains an open question. Here, we longitudinally investigated spontaneous activity and apoptosis in developing cortical cultures, combining extracellular electrophysiology with calcium imaging. These experiments demonstrated that the early occurrence of calcium transients was strongly linked to neuronal survival. Silent neurons exhibited a higher probability of cell death, whereas high frequency spiking and burst behavior were almost exclusively detected in surviving neurons. In local neuronal clusters, activity of neighboring neurons exerted a pro-survival effect, whereas on the functional level, networks with a high modular topology were associated with lower cell death rates. Using machine learning algorithms, cell fate of individual neurons was predictable through the integration of spontaneous activity features. Our results indicate that high frequency spiking activity constrains apoptosis in single neurons through sustained calcium rises and thereby consolidates networks in which a high modular topology is reached during early development. Frontiers Media S.A. 2022-08-10 /pmc/articles/PMC9399774/ /pubmed/36035995 http://dx.doi.org/10.3389/fcell.2022.937761 Text en Copyright © 2022 Warm, Bassetti, Schroer, Luhmann and Sinning. 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 | Cell and Developmental Biology Warm, Davide Bassetti, Davide Schroer, Jonas Luhmann, Heiko J. Sinning, Anne Spontaneous Activity Predicts Survival of Developing Cortical Neurons |
title | Spontaneous Activity Predicts Survival of Developing Cortical Neurons |
title_full | Spontaneous Activity Predicts Survival of Developing Cortical Neurons |
title_fullStr | Spontaneous Activity Predicts Survival of Developing Cortical Neurons |
title_full_unstemmed | Spontaneous Activity Predicts Survival of Developing Cortical Neurons |
title_short | Spontaneous Activity Predicts Survival of Developing Cortical Neurons |
title_sort | spontaneous activity predicts survival of developing cortical neurons |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9399774/ https://www.ncbi.nlm.nih.gov/pubmed/36035995 http://dx.doi.org/10.3389/fcell.2022.937761 |
work_keys_str_mv | AT warmdavide spontaneousactivitypredictssurvivalofdevelopingcorticalneurons AT bassettidavide spontaneousactivitypredictssurvivalofdevelopingcorticalneurons AT schroerjonas spontaneousactivitypredictssurvivalofdevelopingcorticalneurons AT luhmannheikoj spontaneousactivitypredictssurvivalofdevelopingcorticalneurons AT sinninganne spontaneousactivitypredictssurvivalofdevelopingcorticalneurons |