| Literature DB >> 33876374 |
Xiaona Wang1, Zhigang Yang2, Shuanfeng Fang3, Yaodong Zhang4, Jisheng Guo5, Lingshan Gou6.
Abstract
Autism spectrum disorder (ASD) is a heterogeneous group of neurodevelopmental disorder characterized by impaired social interaction, and repetitive or restricted interests and behaviors. Membrane proteins are a significant part of the proteins in cell and play key functions in synaptic transmission. We have recently shown that neuronal nitric oxide synthase (nNOS) expression was reduced in the basolateral amygdala (BLA) of mice following postnatal valproic acid (VPA) exposure. In the current study, we utilized a label-free proteomics approach to identify and quantify surface protein expression in nNOS-positive interneurons between VPA-treated and control mice. Western blot was used to confirm the expression of selected membrane proteins. Our proteomics data revealed differentially expressed surface proteins in nNOS interneurons, e.g. Narp, AMPA-type glutamate (AMPA) receptor subunit GluA4 and Protein kinase C gamma (PKCγ), which were validated by Western blotting in mice treated with VPA. This work will pave the way for further elucidation of the mechanisms of these differentially membrane proteins in nNOS interneurons-medicated ASD.Entities:
Keywords: Autism; Basolateral amygdala; Interneuron; Membrane proteins; NNOS; Proteomics
Year: 2021 PMID: 33876374 DOI: 10.1007/s11064-021-03326-w
Source DB: PubMed Journal: Neurochem Res ISSN: 0364-3190 Impact factor: 3.996