Yankner B A, Dawes L R, Fisher S, Villa-Komaroff L, Oster-Granite M L, Neve R L
Department of Neurology, Harvard Medical School, Boston, MA.
Science. 1989 Jul 28;245(4916):417-20. doi: 10.1126/science.2474201.
Amyloid deposition in senile plaques and the cerebral vasculature is a marker of Alzheimer's disease. Whether amyloid itself contributes to the neurodegenerative process or is simply a by-product of that process is unknown. Pheochromocytoma (PC12) and fibroblast (NIH 3T3) cell lines were transfected with portions of the gene for the human amyloid precursor protein. Stable PC12 cell transfectants expressing a specific amyloid-containing fragment of the precursor protein gradually degenerated when induced to differentiate into neuronal cells with nerve growth factor. Conditioned medium from these cells was toxic to neurons in primary hippocampal cultures, and the toxic agent could be removed by immunoabsorption with an antibody directed against the amyloid polypeptide. Thus, a peptide derived from the amyloid precursor may be neurotoxic.
淀粉样蛋白在老年斑和脑血管中的沉积是阿尔茨海默病的一个标志。淀粉样蛋白本身是导致神经退行性变过程的原因,还是仅仅是该过程的一个副产品,目前尚不清楚。用人类淀粉样前体蛋白基因的部分片段转染嗜铬细胞瘤(PC12)细胞系和成纤维细胞(NIH 3T3)细胞系。当用神经生长因子诱导表达前体蛋白特定含淀粉样蛋白片段的稳定PC12细胞转染子分化为神经元细胞时,它们会逐渐退化。这些细胞的条件培养基对原代海马培养中的神经元有毒,并且可以通过用针对淀粉样多肽的抗体进行免疫吸附来去除毒性因子。因此,源自淀粉样前体的一种肽可能具有神经毒性。