Related Experiment Video
Updated: Jun 27, 2026

Ex utero Electroporation and Whole Hemisphere Explants: A Simple Experimental Method for Studies of Early Cortical Development
Published on: April 3, 2013
Cortex-restricted disruption of NMDAR1 impairs neuronal patterns in the barrel cortex
T Iwasato1, A Datwani, A M Wolf
1Laboratory for Behavioral Genetics, Brain Science Institute, RIKEN, Saitama, Japan.
Cortical N-methyl-D-aspartate receptors (NMDARs) are crucial for sensory map development. Deleting NMDAR1 in excitatory neurons disrupts barrel formation and thalamocortical patterning in the somatosensory cortex.
Area of Science:
- Neuroscience
- Developmental Biology
- Sensory Systems
Background:
- The somatosensory cortex contains topographic representations of sensory inputs like whiskers and paws.
- Neural activity, particularly via N-methyl-D-aspartate receptors (NMDARs), is implicated in sensory map development, but its precise role is debated.
Purpose of the Study:
- To investigate the necessity of cortical NMDARs for the development of somatosensory cortical maps and structures.
Main Methods:
- Generated genetically modified mice with NMDAR1 gene deletion specifically in excitatory cortical neurons.
- Examined the development of sensory pathways in the brainstem, thalamus, and somatosensory cortex using these mice.
Main Results:
- Sensory maps in the brainstem and thalamus developed normally.
- In the cortex, thalamocortical afferents for large whiskers showed some patterning and plasticity, but less distinctly than in controls.
- Patterns for sinus hairs and digits were largely absent.
- Cellular aggregates (barrels) and their boundaries failed to form, even where afferents clustered.
Conclusions:
- Cortical NMDARs are essential for the proper aggregation of layer IV cells into barrels.
- NMDARs are required for the complete development of thalamocortical patterns in the somatosensory cortex.
More Related Videos
06:18Author Spotlight: Deciphering Neural Circuit Formation from Two-Photon Microscopy and Single Neuron Imaging
Published on: November 21, 2023
07:11Examination of Anatomical Features of Retinal Ganglion Cells Under N-methyl-D-aspartic Acid (NMDA)-induced Excitotoxicity
Published on: September 19, 2025
Related Concept Videos
Nucleotide Excision Repair
Mutations
Nuclear Export of mRNA
Nonsense-mediated mRNA Decay
Usually, Upf3 binds to an Exon Junction Complex (EJC) at mRNA splice sites. If a ribosome fully translates the mRNA,...
Nucleotide Excision Repair
Cells are regularly exposed to mutagens—factors in the environment that can damage DNA and generate mutations. UV radiation is one of the most common mutagens and is estimated to introduce a significant number of changes in DNA. These include bends or kinks in the structure, which can block DNA replication or transcription. If these errors are not fixed, the damage can cause mutations, which in turn can result in cancer or disease depending on which sequences are...
GPCR Desensitization