文摘
Metabolism of x3b2;-amyloid peptide (Ax3b2;) 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 x3b2;-amyloid precursor protein (Ax3b2;PP), elevates Ax3b2; levels, and promotes neurodegeneration in old age. These effects were attributed to de novo synthetic pathways; however, the impact on Ax3b2; degradation was not explored. Neprilysin (NEP), a rate-limiting catabolic peptidase is involved in Ax3b2; metabolism in vivo. In the present study we sought to investigate whether accumulation of Ax3b2; 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 Ax3b2;PP, NEP protein and mRNA levels were measured. Additionally, NEP enzymatic activity and Ax3b2; levels were also assessed. Western blot and RT-PCR analysis indicated significant increases in the protein and mRNA expression of Ax3b2;PP, 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 Ax3b2;PP and repression of NEP resulting in the buildup of Ax3b2;.