机构:[1]Program of Molecular Medicine, Affiliated Guangzhou Women and Children’s Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China[2]Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan 2nd Road, Guangzhou 510080, China[3]Institute of Clinical Pharmacology, Guangzhou University of Chinese Medicine, Guangzhou, China[4]Guangdong Province Key Laboratory of Brain Function and Disease, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China[5]China Key Laboratory of Tropical Disease Control (Sun Yat-sen University), Ministry of Education, Guangzhou, China[6]Guangdong Engineering & Technology Research Center for Gene Manipulation and Biomacromolecular Products, Sun Yat-sen University, Guangzhou, China
Alzheimer's disease (AD) is the most common cause of dementia. Pigment epithelium-derived factor (PEDF), a unique neurotrophic protein, decreases with aging. Previous reports have conflicted regarding whether the PEDF concentration is altered in AD patients. In addition, the effect of PEDF on AD has not been documented. Here, we tested serum samples of 31 AD patients and 271 normal controls. We found that compared to PEDF levels in young and middle-aged control subjects, PEDF levels were reduced in old-aged controls and even more so in AD patients. Furthermore, we verified that PEDF expression was much lower and amyloid β-protein (Aβ)42 expression was much higher in senescence-accelerated mouse prone 8 (SAMP8) strain mice than in senescence-accelerated mouse resistant 1 (SAMR1) control strain mice. Accordingly, high levels of Aβ42 were also observed in PEDF knockout (KO) mice. PEDF notably reduced cognitive impairment in the Morris water maze (MWM) and significantly downregulated Aβ42 in SAMP8 mice. Mechanistically, PEDF downregulated presenilin-1 (PS1) expression by inhibiting the c-Jun N-terminal kinase (JNK) pathway. Taken together, our findings demonstrate for the first time that PEDF negatively regulates Aβ42 and that PEDF deficiency with aging might play a crucial role in the development of AD.
基金:
This study was supported by the National Nature Science
Foundation of China, grant numbers: 81471033, 81572342, 81600641,
81770808, 81370945, 81570871, and 81570764; the National Key Sci-
Tech Special Project of China, grant numbers: 2013ZX09102-053 and
2015GKS-355; the Key Project of Nature Science Foundation of
Guangdong Province, China, grant numbers: 2015A030311043 and
2016A030311035; the Guangdong Natural Science Fund, grant numbers:
2014A020212023, 2014A030313073, 2015A030313029, and
2015A030313103; the Guangdong Science Technology Project, grant
numbers: 2017A020215075 and 2015B090903063; Initiate Research
Funds for the Central Universities of China (Youth Program), grant numbers:
13ykpy06, 14ykpy05, and 16ykpy24; the Key Sci-tech Research
Project of Guangzhou Municipality, China, grant numbers:
201508020033, 201707010084, and 201803010017; the Pearl River
Nova Program of Guangzhou Municipality, China, grant number:
201610010186; and the 2017 Milstein Medical Asian American
Partnership Foundation Research Project Award in Translational
Medicine.
语种:
外文
PubmedID:
中科院(CAS)分区:
出版当年[2017]版:
大类|2 区医学
小类|2 区临床神经病学2 区神经科学2 区药学
最新[2025]版:
大类|2 区医学
小类|1 区药学2 区临床神经病学2 区神经科学
第一作者:
第一作者机构:[1]Program of Molecular Medicine, Affiliated Guangzhou Women and Children’s Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China[2]Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan 2nd Road, Guangzhou 510080, China
共同第一作者:
通讯作者:
通讯机构:[1]Program of Molecular Medicine, Affiliated Guangzhou Women and Children’s Hospital, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China[2]Department of Biochemistry, Zhongshan School of Medicine, Sun Yat-sen University, 74 Zhongshan 2nd Road, Guangzhou 510080, China[4]Guangdong Province Key Laboratory of Brain Function and Disease, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, China[5]China Key Laboratory of Tropical Disease Control (Sun Yat-sen University), Ministry of Education, Guangzhou, China[6]Guangdong Engineering & Technology Research Center for Gene Manipulation and Biomacromolecular Products, Sun Yat-sen University, Guangzhou, China
推荐引用方式(GB/T 7714):
Mao Huang,Weiwei Qi,Shuhuan Fang,et al.Pigment Epithelium-Derived Factor Plays a Role in Alzheimer's Disease by Negatively Regulating Aβ42.[J].Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics.2018,15(3):728-741.doi:10.1007/s13311-018-0628-1.
APA:
Mao Huang,Weiwei Qi,Shuhuan Fang,Ping Jiang,Cong Yang...&Guoquan Gao.(2018).Pigment Epithelium-Derived Factor Plays a Role in Alzheimer's Disease by Negatively Regulating Aβ42..Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics,15,(3)
MLA:
Mao Huang,et al."Pigment Epithelium-Derived Factor Plays a Role in Alzheimer's Disease by Negatively Regulating Aβ42.".Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics 15..3(2018):728-741