动物学研究2023,Vol.44Issue(5) :867-881.DOI:10.24272/j.issn.2095-8137.2023.123

Long-term potentiation-based screening identifies neuronal PYGM as a synaptic plasticity regulator participating in Alzheimer's disease

Ting Wang Yun-Qiang Zhou Yong Wang Liang Zhang Xiang Zhu Xiu-Yan Wang Jing-Hui Wang Lin-Kun Han Jian Meng Xian Zhang Hong Luo Qi-Lin Ma Zhan-Xiang Wang Yun-Wu Zhang
动物学研究2023,Vol.44Issue(5) :867-881.DOI:10.24272/j.issn.2095-8137.2023.123

Long-term potentiation-based screening identifies neuronal PYGM as a synaptic plasticity regulator participating in Alzheimer's disease

Ting Wang 1Yun-Qiang Zhou 1Yong Wang 1Liang Zhang 1Xiang Zhu 1Xiu-Yan Wang 1Jing-Hui Wang 1Lin-Kun Han 1Jian Meng 1Xian Zhang 1Hong Luo 1Qi-Lin Ma 2Zhan-Xiang Wang 2Yun-Wu Zhang2
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作者信息

  • 1. Xiamen Key Laboratory of Brain Center,The First Affiliated Hospital of Xiamen University,and Fujian Provincial Key Laboratory of Neurodegenerative Disease and Aging Research,Institute of Neuroscience,School of Medicine,Xiamen University,Xiamen,Fujian 361102,China
  • 2. Xiamen Key Laboratory of Brain Center,The First Affiliated Hospital of Xiamen University,and Fujian Provincial Key Laboratory of Neurodegenerative Disease and Aging Research,Institute of Neuroscience,School of Medicine,Xiamen University,Xiamen,Fujian 361102,China;Fujian Provincial Clinical Research Center for Brain Diseases,The First Affiliated Hospital of Xiamen University,Xiamen,Fujian 361003,China
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Abstract

Synaptic dysfunction is an important pathological hallmark and cause of Alzheimer's disease(AD).High-frequency stimulation(HFS)-induced long-term potentiation(LTP)has been widely used to study synaptic plasticity,with impaired LTP found to be associated with AD.However,the exact molecular mechanism underlying synaptic plasticity has yet to be completely elucidated.Whether genes regulating synaptic plasticity are altered in AD and contribute to disease onset also remains unclear.Herein,we induced LTP in the hippocampal CA1 region of wild-type(WT)and AD model mice by administering HFS to the CA3 region and then studied transcriptome changes in the CA1 region.We identified 89 genes that may participate in normal synaptic plasticity by screening HFS-induced differentially expressed genes(DEGs)in mice with normal LTP,and 43 genes that may contribute to synaptic dysfunction in AD by comparing HFS-induced DEGs in mice with normal LTP and AD mice with impaired LTP.We further refined the 43 genes down to 14 by screening for genes with altered expression in pathological-stage AD mice without HFS induction.Among them,we found that the expression of Pygm,which catabolizes glycogen,was also decreased in AD patients.We further demonstrated that down-regulation of PYGM in neurons impaired synaptic plasticity and cognition in WT mice,while its overexpression attenuated synaptic dysfunction and cognitive deficits in AD mice.Moreover,we showed that PYGM directly regulated energy generation in neurons.Our study not only indicates that PYGM-mediated energy production in neurons plays an important role in synaptic function,but also provides a novel LTP-based strategy to systematically identify genes regulating synaptic plasticity under physiological and pathological conditions.

Key words

Alzheimer's disease/High-frequency stimulation/Long-term potentiation/PYGM/Synaptic plasticity/Transcriptome

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基金项目

National Natural Science Foundation of China(U21A20361)

National Natural Science Foundation of China(82130039)

Fundamental Research Funds for the Central Universities(20720220133)

Natural Science Foundation of Fujian Province(2021J02057)

Science and Technology Plan Projects of Fujian Province(2020Y2015)

2020 Joint Support of Key Projects on Health Care(3502Z20209005)

出版年

2023
动物学研究
中国科学院昆明动物研究所 中国动物学会

动物学研究

CSTPCDCSCD
影响因子:0.582
ISSN:0254-5853
参考文献量2
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