Hypoxia-sensing VGLL4 promotes LDHA-driven lactate production to ameliorate neuronal dysfunction in a cellular model relevant to Alzheimer's disease

作者全名："Tian, Qiuyun; Li, Junjie; Wu, Bin; Wang, Jiaojiao; Xiao, Qian; Tian, Na; Yi, Lilin; Luo, Man; Li, Zhaolun; Pang, Yayan; Shi, Xiuyu; Dong, Zhifang"

作者地址："[Tian, Qiuyun; Li, Junjie; Wu, Bin; Wang, Jiaojiao; Xiao, Qian; Tian, Na; Yi, Lilin; Luo, Man; Li, Zhaolun; Pang, Yayan; Shi, Xiuyu; Dong, Zhifang] Chongqing Med Univ, Childrens Hosp, Pediat Res Inst, Minist Educ,Key Lab Child Dev & Disorders,Natl Cli, Chongqing, Peoples R China; [Dong, Zhifang] Chongqing Med Univ, Inst Brain Sci & Dis, Chongqing, Peoples R China"

通信作者："Dong, ZF (通讯作者)，Chongqing Med Univ, Childrens Hosp, Pediat Res Inst, Minist Educ,Key Lab Child Dev & Disorders,Natl Cli, Chongqing, Peoples R China."

来源：FASEB JOURNAL

ESI学科分类：BIOLOGY & BIOCHEMISTRY

WOS号：WOS:001096502700001

JCR分区：Q1

影响因子：4.4

年份：2023

卷号：37

期号：12

开始页：　

结束页：　

文献类型：Article

关键词：Alzheimer's disease; lactate; LDHA; VGLL4; beta-amyloid

摘要："Alzheimer's disease (AD) is a neurodegenerative disease where abnormal amyloidogenic processing of amyloid-beta precursor protein (APP) occurs and has been linked to neuronal dysfunction. Hypometabolism of glucose in the brain can lead to synaptic loss and neuronal death, which in turn exacerbates energy deficiency and amyloid-beta peptide (A beta) accumulation. Lactate produced by anaerobic glycolysis serves as an energy substrate supporting neuronal function and facilitating neuronal repair. Vestigial-like family member 4 (VGLL4) has been recognized as a key regulator of the hypoxia-sensing pathway. However, the role of VGLL4 in AD remains unexplored. Here, we reported that the expression of VGLL4 protein was significantly decreased in the brain tissue of AD model mice and AD model cells. We further found that overexpression of VGLL4 reduced APP amyloidogenic processing and ameliorated neuronal synaptic damage. Notably, we identified a compromised hypoxia-sensitive capability of LDHA regulated by VGLL4 in the context of AD. Upregulation of VGLL4 increased the response of LDHA to hypoxia and enhanced the expression levels of LDHA and lactate by inhibiting the ubiquitination and degradation of LDHA. Furthermore, the inhibition of lactate production by using sodium oxamate, an inhibitor of LDHA, suppressed the neuroprotective function of VGLL4 by increasing APP amyloidogenic processing. Taken together, our findings demonstrate that VGLL4 exerts a neuroprotective effect by upregulating LDHA expression and consequently promoting lactate production. Thus, this study suggests that VGLL4 may be a novel player involved in molecular mechanisms relevant for ameliorating neurodegeneration."

基金机构："This work was supported by grants from the National Natural Science Foundation of China (32371030 and 82071395), the Natural Science Foundation of Chongqing (cstc2021ycjh-bgzxm0186), and CQMU Program for Youth Innovation in Future Medicine (W0044). We are [32371030, 82071395]; National Natural Science Foundation of China [cstc2021ycjh-bgzxm0186]; Natural Science Foundation of Chongqing [W0044]; CQMU Program for Youth Innovation in Future Medicine"

基金资助正文："This work was supported by grants from the National Natural Science Foundation of China (32371030 and 82071395), the Natural Science Foundation of Chongqing (cstc2021ycjh-bgzxm0186), and CQMU Program for Youth Innovation in Future Medicine (W0044). We are grateful to Dr. Yongyu Wang (Wenzhou Medical University, Wenzhou, China) for providing VGLL4 plasmid, and other members of the Dong Laboratory for the technical support and helpful suggestions."