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PMID: 11238732 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Microglial secreted cathepsin B induces neuronal apoptosis.

Journal of neurochemistry ·Vol. 76 ·No. 5 ·2001-03-00 ·Pages 1475-84

Kingham PJ, Pocock JM

Abstract

Activated microglia release a number of substances that can influence neuronal signalling and survival. Here we report that microglia stimulated with the peptide chromogranin A (CGA), secreted the cysteine protease, cathepsin B. Conditioned medium from CGA exposed microglia was neurotoxic to the HT22 hippocampal cell line and to primary cultures of cerebellar granule neurones. In both neuronal cell types, the neurotoxicity could be significantly attenuated with z-FA-fmk or by depletion of microglial conditioned medium with cathepsin B antibody. Conditioned medium from activated microglia or cathepsin B alone induced neuronal apoptosis and caspase 3 activation. Our data indicate that CGA-activated microglia can trigger neuronal apoptosis and that this may be mediated through the secretion of cathepsin B. Since cathepsins may also play a role in the amyloidogenic processing of amyloid precursor protein, these results may have significance for tissue damage and neuronal loss in the neuropathology of Alzheimer's disease.

MeSH Terms
Animals Animals, Newborn Antibodies/pharmacology Apoptosis/physiology Brain/cytology Cathepsin B/metabolism Cell Line Cells, Cultured Cerebellum/cytology Chromogranin A Chromogranins/pharmacology Culture Media, Conditioned Hippocampus/cytology Microglia/cytology,drug effects,physiology Neurons/cytology,physiology Rats
Chemicals
Antibodies Chromogranin A Chromogranins Culture Media, Conditioned Cathepsin B
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Kingham P J
Department of Neurochemistry, Institute of Neurology, University College London, London, UK.
Pocock J M
Article Info
Journal
Journal of neurochemistry
Abbr.
J Neurochem
ISSN
0022-3042
Published
2001-03-00
Pages
1475-84
Language
English
Region
England
NLM ID
2985190R
Subset
IM
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