In vitro Pb exposure disturbs the balance between Aβ production and elimination: The role of AβPP and neprilysin

详细信息    查看全文

• 作者：Hui Huang^a ; ^b ; Syed Waseem Bihaqi^a ; Liuxin Cui^b ; Nasser H. Zawia^a ; ^{nzawia@uri.edu}
• 关键词：Alzheimer's ; Neprilysin ; Pb ; A&#x3b2 ; &#x3b2 ; -Amyloid precursor protein ; SH-SY5Y cells
• 刊名：Neurotoxicology
• 出版年：2011
• 出版时间：June 2011
• 年：2011
• 卷：32
• 期：3
• 页码：300-306
• 全文大小：548 K

文摘

Metabolism of β-amyloid peptide (Aβ) is closely associated with the pathology and etiology of Alzheimer's disease (AD). Our previous studies on aging primates and rodents have revealed that early life lead exposure increases the expression of the β-amyloid precursor protein (AβPP), elevates Aβ levels, and promotes neurodegeneration in old age. These effects were attributed to de novo synthetic pathways; however, the impact on Aβ degradation was not explored. Neprilysin (NEP), a rate-limiting catabolic peptidase is involved in Aβ metabolism in vivo. In the present study we sought to investigate whether accumulation of Aβ induced by Pb exposure is partially due to its ability to subdue NEP expression and consequently NEP activity. SH-SY5Y cells were exposed to Pb concentrations of 0, 5, 10, 20, and 50 μM for 48 h and AβPP, NEP protein and mRNA levels were measured. Additionally, NEP enzymatic activity and Aβ levels were also assessed. Western blot and RT-PCR analysis indicated significant increases in the protein and mRNA expression of AβPP, which appeared to be concentration and time-dependent, while the protein and mRNA expression of NEP as well as NEP activity declined. These actions of Pb were specific and were not observed when substituted by another metal. These results suggest that Pb causes both the overexpression of AβPP and repression of NEP resulting in the buildup of Aβ.