Role of p75 neurotrophin receptor in the neurotoxicity by beta-amyloid peptides and synergistic effect of inflammatory cytokines

• Published in: The Journal of experimental medicine Vol. 195; no. 7; pp. 907 - 918
• Main Authors: Perini, Giovanni, Della-Bianca, Vittorina, Politi, Valeria, Della Valle, Giuliano, Dal-Pra, Ilaria, Rossi, Filippo, Armato, Ubaldo
• Format: Journal Article
• Language: English
• Published: United States The Rockefeller University Press 01.04.2002
• Subjects: Amyloid beta-Peptides - toxicity; Cell Survival - drug effects; Clone Cells; Cytokines - toxicity; Drug Synergism; Gene Expression Regulation; Humans; Kinetics; Neuroblastoma; Neurons - drug effects; Neurons - pathology; Neurotoxins - toxicity; Original; Peptide Fragments - toxicity; Receptor, Nerve Growth Factor; Receptor, trkA - genetics; Receptor, trkA - physiology; Receptors, Nerve Growth Factor - drug effects; Receptors, Nerve Growth Factor - genetics; Receptors, Nerve Growth Factor - physiology; Recombinant Proteins - metabolism; Sequence Deletion; Transfection; Tumor Cells, Cultured
• ISSN: 0022-1007; 1540-9538
• DOI: 10.1084/jem.20011797

The neurodegenerative changes in Alzheimer's disease (AD) are elicited by the accumulation of beta-amyloid peptides (Abeta), which damage neurons either directly by interacting with components of the cell surface to trigger cell death signaling or indirectly by activating astrocytes and microglia to produce inflammatory mediators. It has been recently proposed that the p75 neurotrophin receptor (p75(NTR)) is responsible for neuronal damage by interacting with Abeta. By using neuroblastoma cell clones lacking the expression of all neurotrophin receptors or engineered to express full-length or various truncated forms of p75(NTR), we could show that p75(NTR) is involved in the direct signaling of cell death by Abeta via the function of its death domain. This signaling leads to the activation of caspases-8 and -3, the production of reactive oxygen intermediates and the induction of an oxidative stress. We also found that the direct and indirect (inflammatory) mechanisms of neuronal damage by Abeta could act synergistically. In fact, TNF-alpha and IL-1beta, cytokines produced by Abeta-activated microglia, could potentiate the neurotoxic action of Abeta mediated by p75(NTR) signaling. Together, our results indicate that neurons expressing p75(NTR), mostly if expressing also proinflammatory cytokine receptors, might be preferential targets of the cytotoxic action of Abeta in AD.