Association of adipocyte enhancer-binding protein 1 with Alzheimer's disease pathology in human hippocampi

被引:29
作者
Shijo, Masahiro [1 ,2 ]
Honda, Hiroyuki [1 ]
Suzuki, Satoshi O. [1 ]
Hamasaki, Hideomi [1 ]
Hokama, Masaaki [3 ]
Abolhassani, Nona [4 ]
Nakabeppu, Yusaku [4 ]
Ninomiya, Toshiharu [5 ]
Kitazono, Takanari [2 ,5 ]
Iwaki, Toru [1 ]
机构
[1] Kyushu Univ, Grad Sch Med Sci, Neurol Inst, Dept Neuropathol, Fukuoka, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Med & Clin Sci, Fukuoka, Japan
[3] Japan Community Healthcare Org, Kyushu Hosp, Dept Neurosurg, Fukuoka, Japan
[4] Kyushu Univ, Med Inst Bioregulat, Dept Immunobiol & Neurosci, Div Neurofunct Genom, Fukuoka, Japan
[5] Kyushu Univ, Grad Sch Med Sci, Ctr Cohort Studies, Fukuoka, Japan
基金
日本学术振兴会;
关键词
AE-binding protein 1; Alzheimer's disease; hippocampus; neurofibrillary tangle; neuron; CARBOXYPEPTIDASE-LIKE PROTEIN; NF-KAPPA-B; AMYLOID BETA-PEPTIDE; GROWTH-FACTOR-BETA; TRANSCRIPTIONAL REPRESSOR; EXPRESSION; AEBP1; MICE; HISAYAMA; DIFFERENTIATION;
D O I
10.1111/bpa.12475
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Adipocyte enhancer binding protein 1 (AEBP1) activates inflammatory responses via the NF-B pathway in macrophages and regulates adipogenesis in preadipocytes. Up-regulation of AEBP1 in the hippocampi of patients with Alzheimer's disease (AD) has been revealed by microarray analyses of autopsied brains from the Japanese general population (the Hisayama study). In this study, we compared the expression patterns of AEBP1 in normal and AD brains, including in the hippocampus, using immunohistochemistry. The subjects were 24 AD cases and 52 non-AD cases. Brain specimens were immunostained with antibodies against AEBP1, tau protein, amyloid protein, NF-B, GFAP and Iba-1. In normal brains, AEBP1 immunoreactivity mainly localized to the perikarya of hippocampal pyramidal neurons, and its expression was elevated in the pyramidal neurons and some astrocytes in AD hippocampi. Although AEBP1 immunoreactivity was almost absent in neurons containing neurofibrillary tangles, AEBP1 was highly expressed in neurons with pretangles and in the tau-immunopositive, dystrophic neurites of senile plaques. Nuclear localization of NF-B was also observed in certain AEBP1-positive neurons in AD cases. Comparison of AD and non-AD cases suggested a positive correlation between the expression level of AEBP1 and the degree of amyloid pathology. These findings imply that AEBP1 protein has a role in the progression of AD pathology.
引用
收藏
页码:58 / 71
页数:14
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