Heparan sulfate from porcine mucosa promotes amyloid-beta clearance in APP/PS1 mice and alleviates Alzheimer's pathology

被引:7
|
作者
Wu, Lidan [1 ]
Jiang, Wenjie [1 ]
Zhao, Na [1 ]
Wang, Fengshan [1 ,2 ,3 ]
机构
[1] Shandong Univ, Inst Biochem & Biotechnol Drugs, Sch Pharmaceut Sci, Key Lab Chem Biol,Minist Educ,Cheeloo Coll Med, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Natl Glycoengn Res Ctr, NMPA Key Lab Qual Res & Evaluat Carbohydrate Base, Jinan 250012, Shandong, Peoples R China
[3] Shandong Univ, Shandong Prov Key Lab Carbohydrate Chem & Glycobi, Jinan 250012, Peoples R China
基金
中国国家自然科学基金;
关键词
Alzheimer's disease; Heparan sulfate; A beta(1-42); Peripheral clearance; Neutrophils phagocytosis; NECROSIS-FACTOR-ALPHA; BLOOD-BRAIN-BARRIER; IN-VIVO; DISEASE; PROTEIN; GLYCOSAMINOGLYCANS; ACCUMULATION; MACROPHAGES; LEUKOCYTES; RECEPTORS;
D O I
10.1016/j.carbpol.2022.119205
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Alzheimer's disease (AD) is a neurodegenerative disease characterized by memory loss and cognitive impairments. Amyloid-beta (A beta) deposition and neurotoxicity play important roles in AD. It has been widely reported that heparan sulfate (HS) proteoglycans play a nonnegligible role in the release, uptake and misfolding of A beta, resulting in the discovery of HS as a therapeutic drug for AD. In this manuscript, HS from porcine mucosa could promote A beta fibrosis and improve the cognitive defects of APPswe/PS1 Delta E9 mice. Furthermore, HS enhanced the phagocytosis of neutrophils to clear A beta(1-42 )from peripheral circulation, reduced peripheral A beta(1-42 )flow to the brain and increased A beta efflux from the brain. Therefore, the deposition of A beta plaques in the brain was decreased. In addition, HS alleviated neutrophil infiltration and reduced neuroinflammation. Conclusively, HS is a promising neuroprotective candidate for AD treatment.
引用
收藏
页数:12
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