Detail of FigS3C_P1_20151031


Project
SSBD:Repository
Title
Time-lapse calcium imaging of olfactory bulb of P1 mouse in vivo expressing GCaMP6f in mitral/tufted cells
Description
Time-lapse calcium imaging of olfactory bulb of postnatal day 1 (P1) mouse expressing GCaMP6f in mitral/tufted cells. Glomerular layer was imaged and spontaneous activity was observed in awake animal.
Release, Updated
2026-08-07
License
CC BY 4.0
Kind
Image data
File Formats
.oib
Data size
823.9 MB

Organism
Mus musculus ( NCBI:txid10090 )
Strain(s)
-
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
calcium ion transport
Cellular Component (CC)
dendrite
Biological Imaging Method
two-photon laser scanning microscopy ( Fbbi:00000254 )
X scale
1.99 micrometer
Y scale
1.99 micrometer
Z scale
-
T scale
0.429 seconds

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
Fujimoto S, Leiwe MN, Aihara S, Sakaguchi R, Muroyama Y, Kobayakawa R, Kobayakawa K, Saito T, Imai T. Activity-dependent local protection and lateral inhibition control synaptic competition in developing mitral cells in mice. Dev Cell. 2023 Jul 24;58(14):1221-1236.e7.
Related paper(s)

Satoshi Fujimoto, Marcus N Leiwe, Shuhei Aihara, Richi Sakaguchi, Yuko Muroyama, Reiko Kobayakawa, Ko Kobayakawa, Tetsuichiro Saito, Takeshi Imai (2023) Activity-dependent local protection and lateral inhibition control synaptic competition in developing mitral cells in mice., Developmental cell

Published in June 7, 2023 (Electronic publication in May 30, 2023, midnight )

(Abstract) In developing brains, activity-dependent remodeling facilitates the formation of precise neuronal connectivity. Synaptic competition is known to facilitate synapse elimination; however, it has remained unknown how different synapses compete with one another within a post-synaptic cell. Here, we investigate how a mitral cell in the mouse olfactory bulb prunes all but one primary dendrite during the developmental remodeling process. We find that spontaneous activity generated within the olfactory bulb is essential. We show that strong glutamatergic inputs to one dendrite trigger branch-specific changes in RhoA activity to facilitate the pruning of the remaining dendrites: NMDAR-dependent local signals suppress RhoA to protect it from pruning; however, the subsequent neuronal depolarization induces neuron-wide activation of RhoA to prune non-protected dendrites. NMDAR-RhoA signals are also essential for the synaptic competition in the mouse barrel cortex. Our results demonstrate a general principle whereby activity-dependent lateral inhibition across synapses establishes a discrete receptive field of a neuron.

Contact
Takeshi Imai, , Kyushu University, , Graduate School of Medical Sciences, , Graduate School of Medical Sciences,
Contributors

OMERO Dataset
OMERO Project
Source