CRISPR/Cas9 based gene editing of Frizzled class receptor 6 (FZD6) reveals its role in depressive symptoms through disrupting Wnt/β-catenin signaling pathway

被引:5
作者
Han, Haijun [1 ,2 ]
Xu, Mengxiang [1 ]
Wang, Ju [3 ]
Li, Ming D. [1 ,4 ]
Yang, Zhongli [1 ]
机构
[1] Zhejiang Univ, Natl Clin Res Ctr Infect Dis,Affiliated Hosp 1, Collaborat Innovat Ctr Diag & Treatment Infect Di, State Key Lab Diag & Treatment Infect Dis,Sch Med, Hangzhou, Peoples R China
[2] Zhejiang Univ City Coll, Sch Med, Key Lab Novel Targets & Drug Study Neural Repair, Hangzhou, Peoples R China
[3] Tianjin Med Univ, Dept Med Engn, Tianjin, Peoples R China
[4] Zhejiang Univ, Res Ctr Air Pollut & Hlth, Hangzhou, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
Depression; FZD6; CRISPR/Cas9; Cell proliferation; Wnt/p-catenin; GLYCOGEN-SYNTHASE KINASE-3-BETA; NEUROTROPHIC FACTOR; GLOBAL BURDEN; BETA-CATENIN; WNT; STRESS; NEUROGENESIS; ACTIVATION; THERAPY; HEALTH;
D O I
10.1016/j.jare.2023.06.001
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
ntroduction: As one of the common psychiatric diseases, depression poses serious threats to human health. Although many genes have been nominated for depression, few of them were investigated in details at the molecular level. Objectives: To demonstrate Frizzled class receptor 6 (FZD6) functions in depression through disrupting Wnt/ p -catenin signal pathway. Methods: The FZD6 edited cell line and mouse model were generated by using CRISPR/Cas9 technique. The expression of key genes and proteins in Wnt/ p -catenin pathway was determined by qRT-PCR and Western blotting, respectively. Animal behavioral tests, including open field test (OFT), elevated plus maze test (EPM), forced swimming test (FST), tail suspension test (TST), and sucrose preference test (SPT), were employed to determine anxiety- and depressive -like behaviors. Immunofluorescent staining was used to assess cell proliferation in the hippocampus of mouse brain. Results: Among patients with depression, FZD6, one of the receptors of Wnt ligand, was significantly decreased. In CRISPR/Cas9-based FZD6 knockdown cells, we showed that FZD6 plays a significant role in regulating expression of genes involved in Wnt/ p -catenin pathway. Subsequently behavioral studies on Fzd6 knockdown mice (with a 5-nudeotide deletion; Fzd6 -A5) revealed significant changes in depressive symptoms, including increased immobility duration in FST, less preference of sucrose in SPT, reduction of distance traveled in OFT, and decreased time spent in open arms in EPM. Immunofluorescent staining showed decreased cell proliferation in the hippocampus of Fzd6 -A5 mice with reduced number of Ki67 ' and PCNA ' cells. Moreover, decreased Gsk3 beta mRNA expression, phosphorylated GSK3 B , and cytoplasmic B -catenin in the hippocampus of Fzd6 -A5 mice provided further evidence supporting the role of Fzd6 in depression. Conclusion: Together, above findings proved the significant role of FZD6 in depression through its effect on hippocampal cell proliferation and its ability to regulate canonical Wnt/ B -catenin pathway. 2024 The Authors. Published by Elsevier B.V. on behalf of Cairo University. This is an open access article under the CC BY -NC -ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:129 / 138
页数:10
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