Abstract

Major depressive disorders are emerging health problems that affect millions of people worldwide. However, treatment options and targets for drug development are limited. Impaired adult hippocampal neurogenesis is emerging as a key contributor to the pathology of major depressive disorders. We previously demonstrated that increasing the expression of the multifunctional scaffold protein Axis inhibition protein (Axin) by administration of the small molecule XAV939 enhances embryonic neurogenesis and affects social interaction behaviors. This prompted us to examine whether increasing Axin protein level can enhance adult hippocampal neurogenesis and thus contribute to mood regulation. Here, we report that stabilizing Axin increases adult hippocampal neurogenesis and exerts an antidepressant effect. Specifically, treating adult mice with XAV939 increased the amplification of adult neural progenitor cells and neuron production in the hippocampus under both normal and chronic stress conditions. Furthermore, XAV939 injection in mice ameliorated depression-like behaviors induced by chronic restraint stress. Thus, our study demonstrates that Axin/XAV939 plays an important role in adult hippocampal neurogenesis and provides a potential therapeutic approach for mood-related disorders.

Details

Title
Increased Axin expression enhances adult hippocampal neurogenesis and exerts an antidepressant effect
Author
Wei-Wei, Chen 1 ; Wing-Yu, Fu 1 ; Yi-Ting, Su 1 ; Wei-Qun, Fang 1 ; Fu Amy K Y 2 ; Ip, Nancy Y 2 

 The Hong Kong University of Science and Technology, Clear Water Bay, Division of Life Science, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450); The Hong Kong University of Science and Technology, Clear Water Bay, Molecular Neuroscience Center, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450); State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450) 
 The Hong Kong University of Science and Technology, Clear Water Bay, Division of Life Science, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450); The Hong Kong University of Science and Technology, Clear Water Bay, Molecular Neuroscience Center, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450); State Key Laboratory of Molecular Neuroscience, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China (GRID:grid.24515.37) (ISNI:0000 0004 1937 1450); Guangdong Provincial Key Laboratory of Brain Science, Disease and Drug Development, HKUST Shenzhen Research Institute, Shenzhen, Guangdong, China (GRID:grid.495521.e) 
Publication year
2019
Publication date
Feb 2019
Publisher
Nature Publishing Group
e-ISSN
20452322
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2350329051
Copyright
This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.