Detail of Fig4H_RhoABC-KO_RhoA_2


Project
SSBD:Repository
Title
Z-series images of RhoABC-knockout and RhoA-rescued mouse brain at P6 in which mitral cells were labed by tdTomato
Description
Z-series images of RhoA, RhoB, and RhoC knockout mouse brain at P6 in which mitral cells were labed by tdTomato. RhoA, B, and C were knocked out by using CRISPR-Cas9 and in utero electroporation. In this experoment, CRISPR- resistant-pCAG-RhoA was also introduced by in utero electroporation to test effect of the compensatory exprssion of RhoA. The cleared olfactory bulb was stained with DAPI.
Release, Updated
2026-08-07
License
CC BY 4.0
Kind
Image data
File Formats
.lif
Data size
1.8 GB

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

Datatype
-
Molecular Function (MF)
Biological Process (BP)
neuron development neuron remodeling
Cellular Component (CC)
cell body dendrite
Biological Imaging Method
confocal microscopy ( Fbbi:00000251 )
X scale
0.568 micrometer
Y scale
0.569 micrometer
Z scale
5 micrometer
T scale
-

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