Journal
JOURNAL OF NIPPON MEDICAL SCHOOL
Volume 82, Issue 2, Pages 92-99Publisher
MEDICAL ASSOC NIPPON MEDICAL SCH
DOI: 10.1272/jnms.82.92
Keywords
amygdala; anxiety; autism spectrum disorder; microglia; minocycline
Categories
Funding
- MEXT KAKENHI [25460345]
- Japan Science and Technology Agency, Core Research for Evolutional Science and Technology
- Grants-in-Aid for Scientific Research [25242077, 25460345, 26670165] Funding Source: KAKEN
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Background and Purpose: Autism spectrum disorder (ASD) is a neurodevelopmental disorder with a strong genetic basis. Although anxiety is a common major psychiatric condition in ASD, the underlying mechanisms of the anxiety are poorly understood. In individuals with ASD, evidence indicates a structural abnormality in the amygdala, a key component involved in anxiety and social behavior. Microglia, which are central nervous system-resident immune cells implicated in neurodevelopmental processes, are also reportedly altered in ASD. In the present study, we examined the involvement of microglia in the anxiety-related behaviors of ASD model mouse. Methods: Mice that have a 6.3-Mb paternal duplication (patDp/+) corresponding to human chromosome 15q11-q13 were used as an ASD model. Thai, a microglial activation marker, was examined in the amygdala using immunofluorescence. Effects of perinatal treatment with minocycline, a microglial modulator, on anxiety-related behaviors were examined in neonatal and adolescent patDp/+ mice. Results: In patDp/+ mice, Iba1 was decreased in the basolateral amygdala at postnatal day 7, but not at postnatal days 37-40. Perinatal treatment with minocycline restored the lba1 expression and reduced anxiety-related behaviors in patDp/+ adolescent mice. Conclusions: Perinatal microglia in the basolateral amygdala may play a pathogenic role in the anxiety observed in a mouse model of ASD with duplication of human chromosome 15q11-q13.
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