Author Type

Graduate Student

Date of Award

Spring 4-28-2022

Document Type

Thesis

Publication Status

Version of Record

Degree Name

Master of Science (MS)

Department

Biological Sciences

First Advisor

Gregory Macleod

Abstract

TBR1 is a high-confidence risk gene for autism spectrum disorder (ASD). Haploinsufficient (Tbr1+/-) mice exhibit ASD-characteristic behavioral changes that are often associated with amygdala circuit dysfunction. We investigated excitatory synaptic transmission in the thalamic-lateral amygdala pathway of these mice. Preliminary data showed increased AMPA receptor-mediated synaptic current in 4-week-old Tbr1+/- mice. To examine the molecular basis for this change, we measured the quantity, proportion, and density of synaptic AMPARs and NMDARs in both Tbr1+/- and wild type mice using freeze-fracture replica immunogold labeling. Receptor quantification and synaptic area demarcation were performed sing supervised deep-learning networks. Our results showed no significant difference in the density or proportion of AMPA receptors at synapses of the Tbr1+/- mice.

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