凝集素
生物
疾病
信号转导
阿尔茨海默病
神经科学
免疫学
细胞生物学
遗传学
医学
细胞凋亡
内科学
作者
Seyed Mohammad Iman Moezzi,Negin Mozafari,Seyed-Mostafa Fazel-Hoseini,Sadra Nadimi Parashkouhi,Hosein Abbasi,Hajar Ashrafi,Amir Azadi
标识
DOI:10.1021/acschemneuro.0c00637
摘要
Apolipoprotein J (ApoJ), or clusterin, is one of the main apolipoproteins in the brain. It is synthesized and released from astrocytes in a healthy brain, and its expression increases in neurodegenerative disorders. Genetic evidence has suggested an association between ApoJ polymorphism and the risk of Alzheimer's disease (AD)—it is now considered the third main genetic risk factor for late-onset AD. However, the role of ApoJ overexpression in the state of disorder, toxicity, or protection is not yet clear. Since ApoJ plays different roles in AD, we review the function of ApoJ using different cell signaling pathways in AD and outline its paradoxical roles in AD. ApoJ helps in amyloid-beta (Aβ) clearance. Vice versa, ApoJ gene knock-out causes fibrillary Aβ reduction and prevents Aβ-induced neuron cell death. Understanding ApoJ, through various cellular signaling pathways, creates a new perspective on AD's cellular principles. The overall message is that ApoJ can be a valuable tool in controlling AD.
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