Detail of Fig5ABC_DORA-RhoA_NMDA_7


Project
SSBD:Repository
Title
FRET imaging of RhoA activity in mitral cells after NMDA stimulation using the DORA-RhoA biosensor in the presence of TTX
Description
Time-lapse images of RhoA activity in olfactory bulb slice from P3 mouse. To stimurate NMDA receptors, the slice was treated with NMDA and glycine during imaging. RhoA activity was studied with DORA-RhoA, a FRET biosensor for RhoA.
Release, Updated
2026-08-07
License
CC BY 4.0
Kind
Image data
File Formats
.oib
Data size
411.4 MB

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

Datatype
-
Molecular Function (MF)
Biological Process (BP)
postsynaptic signal transduction
Cellular Component (CC)
cell body dendrite
Biological Imaging Method
two-photon laser scanning microscopy ( Fbbi:00000254 )
X scale
0.497 micrometer
Y scale
0.497 micrometer
Z scale
-
T scale
5 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