Identification of Cathepsin B as a Mediator of Neuronal Death Induced by Aβ-activated Microglial Cells Using a Functional Genomics Approach

• Published in: The Journal of biological chemistry Vol. 279; no. 7; p. 5565
• Main Authors: Li Gan, Shiming Ye, Alan Chu, Kristin Anton, Saili Yi, Valerie A. Vincent, David von Schack, Daniel Chin, Joseph Murray, Scott Lohr, Laszlo Patthy, Mirella Gonzalez-Zulueta, Karoly Nikolich, Roman Urfer
• Format: Journal Article
• Language: English
• Published: American Society for Biochemistry and Molecular Biology 13.02.2004
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M306183200

Alzheimer's disease is a progressive neurodegenerative disease characterized by senile plaques, neurofibrillary tangles, dystrophic neurites, and reactive glial cells. Activated microglia are found to be intimately associated with senile plaques and may play a central role in mediating chronic inflammatory conditions in Alzheimer's disease. Activation of cultured murine microglial BV2 cells by freshly sonicated Aβ42 results in the secretion of neurotoxic factors that kill primary cultured neurons. To understand molecular pathways underlying Aβ-induced microglial activation, we analyzed the expression levels of transcripts isolated from Aβ42-activated BV2 cells using high density filter arrays. The analysis of these arrays identified 554 genes that are transcriptionally up-regulated by Aβ42 in a statistically significant manner. Quantitative reverse transcription-PCR was used to confirm the regulation of a subset of genes, including cysteine proteases cathepsin B and cathepsin L, tissue inhibitor of matrix metalloproteinase 2, cytochrome c oxidase, and allograft inflammatory factor 1. Small interfering RNA-mediated silencing of the cathepsin B gene in Aβ-activated BV2 cells diminished the microglial activation-mediated neurotoxicity. Moreover, CA-074, a specific cathepsin B inhibitor, also abolished the neurotoxic effects caused by Aβ42-activated BV2 cells. Our results suggest an essential role for secreted cathepsin B in neuronal death mediated by Aβ-activated inflammatory response.