Lipid rafts participate in aberrant degradative autophagic-lysosomal pathway of amyloid-beta peptide in Alzheimer's disease

被引:11
作者
Zhou, Xin [1 ]
Yang, Chun [1 ]
Liu, Yufeng [1 ]
Li, Peng [1 ]
Yang, Huiying [1 ]
Dai, Jingxing [1 ]
Qu, Rongmei [1 ]
Yuan, Lin [1 ]
机构
[1] Southern Med Univ, Sch Basic Med Sci, Dept Human Anat Histol & Embryol, Guangzhou 510515, Guangdong, Peoples R China
关键词
nerve regeneration; lipid rafts; amyloid precursor protein; autophagy; lysosome; Alzheimer's disease; Two-system Theory; amyloid beta peptide; autophagosome; National Financial Major Project of China; neural regeneration; BLOOD-BRAIN-BARRIER; PRECURSOR PROTEIN; NEURODEGENERATIVE DISEASE; CONNECTIVE TISSUES; OXIDATIVE STRESS; APOLIPOPROTEIN-E; PLASMA-MEMBRANE; GM1; GANGLIOSIDE; GAMMA-SECRETASE; MOUSE MODEL;
D O I
10.4103/1673-5374.125335
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Amyloid-beta peptide is the main component of amyloid plaques, which are found in Alzheimer's disease. The generation and deposition of amyloid-beta is one of the crucial factors for the onset and progression of Alzheimer's disease. Lipid rafts are glycolipid-rich liquid domains of the plasma membrane, where certain types of protein tend to aggregate and intercalate. Lipid rafts are involved in the generation of amyloid-beta oligomers and the formation of amyloid-beta peptides. In this paper, we review the mechanism by which lipid rafts disturb the aberrant degradative autophagic-lysosomal pathway of amyloid-beta, which plays an important role in the pathological process of Alzheimer's disease. Moreover, we describe this mechanism from the view of the Two-system Theory of fasciology and thus, suggest that lipid rafts may be a new target of Alzheimer's disease treatment.
引用
收藏
页码:92 / 100
页数:9
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