Summary of ssbd-repos-000326

Name
URL
DOI

Title
Imaging data in the paper, "Microglia are dispensable for developmental dendrite pruning of mitral cells in mice" (Niiyama et al., 2023).
Description

Neuronal morphology data of olfactory mitral cells or Layer4 neurons in the barrel cortex, immunostaining imaging data of olfactory bulb.

Submited Date
2023-10-17
Release Date
2023-10-27
Updated Date
-
License
Funding information
-
File formats
lif, DAT, pzf
Data size
511.0 GB

Organism
Mus musculus
Strain
-
Cell Line
-
Genes
-
Proteins
-

GO Molecular Function (MF)
-
GO Biological Process (BP)
-
GO Cellular Component (CC)
-
Study Type
-
Imaging Methods
-

Method Summary
-
Related paper(s)

Tetsushi Niiyama, Satoshi Fujimoto, Takeshi Imai (2023) Microglia are dispensable for developmental dendrite pruning of mitral cells in mice., eNeuro

Published in 2023 Oct 27 (Electronic publication in Oct. 27, 2023, midnight )

(Abstract) During early development, neurons in the brain often form excess synaptic connections. Later, they strengthen some connections while eliminating others to build functional neuronal circuits. In the olfactory bulb, a mitral cell initially extends multiple dendrites to multiple glomeruli but eventually forms a single primary dendrite through the activity-dependent dendrite pruning process. Recent studies have reported that microglia facilitate synapse pruning during the circuit remodeling in some systems. It has remained unclear whether microglia are involved in the activity-dependent dendrite pruning in the developing brains. Here, we examined whether microglia are required for the developmental dendrite pruning of mitral cells in mice. To deplete microglia in the fetal brain, we treated mice with a CSF1R inhibitor, PLX5622, from pregnancy. Microglia were reduced by >90% in mice treated with PLX5622. However, dendrite pruning of mitral cells was not significantly affected. Moreover, we found no significant differences in the number, density, and size of excitatory synapses formed in mitral cell dendrites. We also found no evidence for the role of microglia in the activity-dependent dendrite remodeling of layer 4 neurons in the barrel cortex. In contrast, the density of excitatory synapses (dendritic spines) in granule cells in the olfactory bulb was significantly increased in mice treated with PLX5622 at P6, suggesting a role for the regulation of dendritic spines. Our results indicate that microglia do not play a critical role in activity-dependent dendrite pruning at the neurite level during early postnatal development in mice.Significance StatementSynapse elimination is essential for activity-dependent circuit remodeling in the developing brains of mammals. Recent studies suggested that microglia play a critical role in the synapse elimination. This study found that microglia are dispensable for the activity-dependent dendrite pruning in developing mitral cells and layer 4 neurons in the barrel cortex. Thus, microglia are not critical for activity-dependent dendrite pruning at the neurite level during normal developmental process.

Contact(s)
Takeshi Imai
Organization(s)
Kyushu Univerisity
Image Data Contributors
Satoshi Fujimoto, Tetsushi Niiyama
Quantitative Data Contributors

Download files
Download zipped files