Diminished activity-dependent BDNF signaling differentially causes autism-like behavioral deficits in male and female mice

• Published in: Frontiers in psychiatry Vol. 14; p. 1182472
• Main Authors: Ma, Kaijie, Taylor, Connie, Williamson, Mark, Newton, Samuel S, Qin, Luye
• Format: Journal Article
• Language: English
• Published: Switzerland Frontiers Media S.A 03-05-2023
• Subjects: activity-dependent neural signaling; anxiety; autism spectrum disorder; BDNF; Psychiatry; social behaviors; Val66Met; activity-dependent neural signaling; anxiety; social behaviors; Val66Met; cognition; BDNF; sex; autism spectrum disorder
• ISSN: 1664-0640; 1664-0640
• DOI: 10.3389/fpsyt.2023.1182472

Autism spectrum disorder (ASD) is a group of neurodevelopmental disorders with strong genetic heterogeneity and more prevalent in males than females. Recent human genetic studies have identified multiple high-risk genes for ASD, which produce similar phenotypes, indicating that diverse genetic factors converge to common molecular pathways. We and others have hypothesized that activity-dependent neural signaling is a convergent molecular pathway dysregulated in ASD. However, the causal link between diminished activity-dependent neural signaling and ASD remains unclear. Brain-derived neurotrophic factor (BDNF) is a key molecule mediating activity-dependent neural signaling. We therefore hypothesize that diminished activity-dependent BDNF signaling could confer autism-like behavioral deficits. Here, we investigated the effect of diminished activity-dependent BDNF signaling on autism-like behavioral deficits by using mice with genetic knock-in of a human BDNF methionine (Met) allele, which has decreased activity-dependent BDNF release without altering basal BDNF level. Compared with wild-type (WT) controls, diminished activity-dependent BDNF signaling similarly induced anxiety-like behaviors in male and female mice. Notably, diminished activity-dependent BDNF signaling differentially resulted in autism-like social deficits and increased self-grooming in male and female mice, and male mice were more severe than female mice. Again, sexually dimorphic spatial memory deficits were observed in female BDNF
mice, but not in male BDNF
mice. Our study not only reveals a causal link between diminished activity-dependent BDNF signaling and ASD-like behavioral deficits, but also identifies previously underappreciated sex-specific effect of diminished activity-dependent BDNF signaling in ASD. These mice with genetic knock-in of the human BDNF Met variant provide a distinct mouse model for studying the cellular and molecular mechanisms underlying diminished activity-dependent neural signaling, the common molecular pathway dysregulated in ASD.