NEGR1 Modulates Mouse Affective Discrimination by Regulating Adult Olfactory Neurogenesis.

BACKGROUND

Affective recognition and sensory processing are impaired in people with autism. However, no mouse model of autism comanifesting these symptoms is available, thereby limiting the exploration of the relationship between affective recognition and sensory processing in autism and the molecular mechanisms involved.

METHODS

With mice, we conducted the affective state discrimination test and an odor habituation/dishabituation test. Data were analyzed using the -means clustering method. We also employed a whole-cell patch clamp and bromodeoxyuridine incorporation assay to investigate underlying mechanisms.

RESULTS

When encountering mice exposed to restraint stress or chronic pain, wild-type mice discriminated between them by either approaching the stressed mouse or avoiding the painful mouse, whereas mice showed unbiased social interactions with them. Next, we demonstrated that both wild-type and mice used their olfaction for social interaction in the experimental context, but mice showed aberrant olfactory habituation and dishabituation against social odors. In electrophysiological studies, inhibitory inputs to the mitral cells in the olfactory bulb were increased in mice compared with wild-type mice, and subsequently their excitability was decreased. As a potential underlying mechanism, we found that adult neurogenesis in the subventricular zone was diminished in mice, which resulted in decreased integration of newly generated inhibitory neurons in the olfactory bulb.

CONCLUSIONS

NEGR1 contributes to mouse affective recognition, possibly by regulating olfactory neurogenesis and subsequent olfactory sensory processing. We propose a novel neurobiological mechanism of autism-related behaviors based on disrupted adult olfactory neurogenesis.