Utilizing 2D-region-based CNNs for automatic dendritic spine detection in 3D live cell imaging.
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
22 Nov 2023
22 Nov 2023
Historique:
received:
14
02
2023
accepted:
08
11
2023
medline:
24
11
2023
pubmed:
23
11
2023
entrez:
22
11
2023
Statut:
epublish
Résumé
Dendritic spines are considered a morphological proxy for excitatory synapses, rendering them a target of many different lines of research. Over recent years, it has become possible to simultaneously image large numbers of dendritic spines in 3D volumes of neural tissue. In contrast, currently no automated method for 3D spine detection exists that comes close to the detection performance reached by human experts. However, exploiting such datasets requires new tools for the fully automated detection and analysis of large numbers of spines. Here, we developed an efficient analysis pipeline to detect large numbers of dendritic spines in volumetric fluorescence imaging data acquired by two-photon imaging in vivo. The core of our pipeline is a deep convolutional neural network that was pretrained on a general-purpose image library and then optimized on the spine detection task. This transfer learning approach is data efficient while achieving a high detection precision. To train and validate the model we generated a labeled dataset using five human expert annotators to account for the variability in human spine detection. The pipeline enables fully automated dendritic spine detection reaching a performance slightly below that of the human experts. Our method for spine detection is fast, accurate and robust, and thus well suited for large-scale datasets with thousands of spines. The code is easily applicable to new datasets, achieving high detection performance, even without any retraining or adjustment of model parameters.
Identifiants
pubmed: 37993550
doi: 10.1038/s41598-023-47070-3
pii: 10.1038/s41598-023-47070-3
pmc: PMC10665560
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
20497Subventions
Organisme : Deutsche Forschungsgemeinschaft
ID : SPP 2041
Organisme : Deutsche Forschungsgemeinschaft
ID : SPP 2041
Organisme : Deutsche Forschungsgemeinschaft
ID : CRC 1080
Organisme : Deutsche Forschungsgemeinschaft
ID : CRC 1080
Organisme : Deutsche Forschungsgemeinschaft
ID : SPP 2041
Organisme : Deutsche Forschungsgemeinschaft
ID : SPP 2041
Informations de copyright
© 2023. The Author(s).
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