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Conditional Genetic Transsynaptic Tracing in the Embryonic Mouse Brain
Published on: December 22, 2014
Trpc2 gene impacts on maternal aggression, accessory olfactory bulb anatomy and brain activity
1Center for Women's Health Research, University of Wisconsin-Madison, WI 53706, USA. nshasen@wisc.edu
Genes, Brain, and Behavior
|October 6, 2009
Summary
The Trpc2 gene is crucial for maternal aggression and brain activity in mice. Loss of this gene impairs aggression and alters specific brain structures involved in sensory processing and behavior.
Area of Science:
- Neuroscience
- Genetics
- Behavioral Biology
Background:
- The Trpc2 gene encodes an ion channel in the vomeronasal organ (VNO), essential for pheromone detection.
- Trpc2 knockout (KO) mice are used to study VNO function in pheromonally mediated behaviors.
- Previous research has not examined the impact of Trpc2 on brain activity.
Purpose of the Study:
- To investigate the effect of Trpc2 gene deletion on brain activity in maternal aggression.
- To analyze Fos immunoreactivity (Fos-IR) in specific brain regions of lactating dams.
- To correlate anatomical changes in the accessory olfactory bulb (AOB) with behavioral deficits.
Main Methods:
- Intruder tests were performed on lactating Trpc2 KO and wild-type dams.
- Fos-IR was quantified in the vomeronasal amygdala, hypothalamus, olfactory regions, and AOB.
- Home-cage observations were conducted to assess maternal behaviors like nest-building.
Main Results:
- Trpc2 deletion significantly reduced maternal aggression, confirming previous findings.
- Differential hypotrophy of the AOB's glomerular layer was observed in KO mice, with anterior and posterior regions showing distinct alterations.
- Fos-IR analysis revealed Trpc2 deletion impacts 21 brain regions involved in emotion, aggression, and olfaction.
- KO dams exhibited deficits in nest-building behavior, suggesting a role for pup pheromones.
Conclusions:
- The Trpc2 gene plays a significant role in modulating maternal aggression and associated brain activity.
- Altered AOB anatomy in Trpc2 KO mice suggests residual VNO function.
- VNO signals mediated by Trpc2 influence a widespread neural network involved in sensory processing and maternal behaviors.

