Tags

Type your tag names separated by a space and hit enter

Identification of the key molecules involved in chronic copper exposure-aggravated memory impairment in transgenic mice of Alzheimer's disease using proteomic analysis.
J Alzheimers Dis. 2015; 44(2):455-69.JA

Abstract

Alzheimer's disease (AD) is the most common neurodegenerative disease characterized by a progressive impairment of cognitive functions including spatial learning and memory. Excess copper exposure accelerates the development of AD; however, the potential mechanisms by which copper exacerbates the symptoms of AD remain unknown. In this study, we explored the effects of chronic copper exposure on cognitive function by treating 6 month-old triple AD transgenic (3xTg-AD) mice with 250 ppm copper sulfate in drinking water for 6 months, and identified several potential key molecules involved in the effects of chronic copper exposure on memory by proteomic analysis. The behavioral test showed that chronic copper exposure aggravated memory impairment of 3xTg-AD mice. Two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with mass spectrometry revealed a total of 44 differentially expressed proteins (18 upregulated and 26 down-regulated) in hippocampus between the wild-type (WT) mice and non-exposed 3xTg-AD mice. A total of 40 differentially expressed proteins were revealed (20 upregulated and 20 down-regulated) in hippocampus between copper exposed and non-exposed 3xTg-AD mice. Among these differentially expressed proteins, complexin-1 and complexin-2, two memory associated proteins, were significantly decreased in hippocampus of 3xTg-AD mice compared with the WT mice. Furthermore, the expression of these two proteins was further down-regulated in 3xTg-AD mice when exposed to copper. The abnormal expression of complexin-1 and complexin-2 identified by proteomic analysis was verified by western blot analysis. Taken together, our data showed that chronic copper exposure accelerated memory impairment and altered the expression of proteins in hippocampus in 3xTg-AD mice. The functional analysis on the differentially expressed proteins suggested that complexin-1 and complexin-2 may be the key molecules involved in chronic copper exposure-aggravated memory impairment in AD.

Authors+Show Affiliations

College of Pharmacy, Jinan University, Guangdong, China Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.Shen Zhen Kai-Tuo Biotech, Shenzhen, China Guang Zhou Kai-Tuo Biotech, Guangzhou, China.College of Pharmacy, Jinan University, Guangdong, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China College of Life Sciences, Shenzhen University, Shenzhen, China.Laboratory of Neurodegenerative Diseases, Department of Anatomy, The University of Hong Kong, Pokfulam, Hong Kong SAR, China.Department of Neurology, Shanghai Jiaotong University Affiliated the Sixth Hospital, Shanghai, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen, China.

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

25352456

Citation

Yu, Jun, et al. "Identification of the Key Molecules Involved in Chronic Copper Exposure-aggravated Memory Impairment in Transgenic Mice of Alzheimer's Disease Using Proteomic Analysis." Journal of Alzheimer's Disease : JAD, vol. 44, no. 2, 2015, pp. 455-69.
Yu J, Luo X, Xu H, et al. Identification of the key molecules involved in chronic copper exposure-aggravated memory impairment in transgenic mice of Alzheimer's disease using proteomic analysis. J Alzheimers Dis. 2015;44(2):455-69.
Yu, J., Luo, X., Xu, H., Ma, Q., Yuan, J., Li, X., Chang, R. C., Qu, Z., Huang, X., Zhuang, Z., Liu, J., & Yang, X. (2015). Identification of the key molecules involved in chronic copper exposure-aggravated memory impairment in transgenic mice of Alzheimer's disease using proteomic analysis. Journal of Alzheimer's Disease : JAD, 44(2), 455-69. https://doi.org/10.3233/JAD-141776
Yu J, et al. Identification of the Key Molecules Involved in Chronic Copper Exposure-aggravated Memory Impairment in Transgenic Mice of Alzheimer's Disease Using Proteomic Analysis. J Alzheimers Dis. 2015;44(2):455-69. PubMed PMID: 25352456.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Identification of the key molecules involved in chronic copper exposure-aggravated memory impairment in transgenic mice of Alzheimer's disease using proteomic analysis. AU - Yu,Jun, AU - Luo,Xiaobin, AU - Xu,Hua, AU - Ma,Quan, AU - Yuan,Jianhui, AU - Li,Xuling, AU - Chang,Raymond Chuen-Chung, AU - Qu,Zhongsen, AU - Huang,Xinfeng, AU - Zhuang,Zhixiong, AU - Liu,Jianjun, AU - Yang,Xifei, PY - 2014/10/30/entrez PY - 2014/10/30/pubmed PY - 2015/9/22/medline KW - Alzheimer's disease KW - copper KW - memory impairment KW - two-dimensional fluorescence difference gel electrophoresis SP - 455 EP - 69 JF - Journal of Alzheimer's disease : JAD JO - J. Alzheimers Dis. VL - 44 IS - 2 N2 - Alzheimer's disease (AD) is the most common neurodegenerative disease characterized by a progressive impairment of cognitive functions including spatial learning and memory. Excess copper exposure accelerates the development of AD; however, the potential mechanisms by which copper exacerbates the symptoms of AD remain unknown. In this study, we explored the effects of chronic copper exposure on cognitive function by treating 6 month-old triple AD transgenic (3xTg-AD) mice with 250 ppm copper sulfate in drinking water for 6 months, and identified several potential key molecules involved in the effects of chronic copper exposure on memory by proteomic analysis. The behavioral test showed that chronic copper exposure aggravated memory impairment of 3xTg-AD mice. Two-dimensional fluorescence difference gel electrophoresis (2D-DIGE) coupled with mass spectrometry revealed a total of 44 differentially expressed proteins (18 upregulated and 26 down-regulated) in hippocampus between the wild-type (WT) mice and non-exposed 3xTg-AD mice. A total of 40 differentially expressed proteins were revealed (20 upregulated and 20 down-regulated) in hippocampus between copper exposed and non-exposed 3xTg-AD mice. Among these differentially expressed proteins, complexin-1 and complexin-2, two memory associated proteins, were significantly decreased in hippocampus of 3xTg-AD mice compared with the WT mice. Furthermore, the expression of these two proteins was further down-regulated in 3xTg-AD mice when exposed to copper. The abnormal expression of complexin-1 and complexin-2 identified by proteomic analysis was verified by western blot analysis. Taken together, our data showed that chronic copper exposure accelerated memory impairment and altered the expression of proteins in hippocampus in 3xTg-AD mice. The functional analysis on the differentially expressed proteins suggested that complexin-1 and complexin-2 may be the key molecules involved in chronic copper exposure-aggravated memory impairment in AD. SN - 1875-8908 UR - https://www.unboundmedicine.com/medline/citation/25352456/Identification_of_the_key_molecules_involved_in_chronic_copper_exposure_aggravated_memory_impairment_in_transgenic_mice_of_Alzheimer's_disease_using_proteomic_analysis_ L2 - https://content.iospress.com/openurl?genre=article&id=doi:10.3233/JAD-141776 DB - PRIME DP - Unbound Medicine ER -