Glutamate induces rapid loss of axonal neurofilament proteins from cortical neurons in vitro

RS Chung, GH McCormack, AE King, AK West… - Experimental …, 2005 - Elsevier
RS Chung, GH McCormack, AE King, AK West, JC Vickers
Experimental neurology, 2005Elsevier
One of the primary hallmarks of glutamate excitotoxicity is degradation of the neuronal
cytoskeleton. Using a tissue culture approach, we have investigated the relationship
between excitotoxicity and cytoskeletal degradation within axons, with particular reference to
the axon specific neurofilament proteins. Neurofilaments were rapidly lost from axons over a
24-h period in response to excitotoxic insult (as observed by immunocytochemistry and
western blotting), while other axonal cytoskeletal markers (such as βIII-tubulin) remained …
One of the primary hallmarks of glutamate excitotoxicity is degradation of the neuronal cytoskeleton. Using a tissue culture approach, we have investigated the relationship between excitotoxicity and cytoskeletal degradation within axons, with particular reference to the axon specific neurofilament proteins. Neurofilaments were rapidly lost from axons over a 24-h period in response to excitotoxic insult (as observed by immunocytochemistry and western blotting), while other axonal cytoskeletal markers (such as βIII-tubulin) remained intact. Treatment with kainic acid and NMDA, or complementary experiments using the pharmacological glutamate receptors blockers CNQX (kainate/AMPA receptor antagonist) and MK-801 (NMDA receptor antagonist), demonstrated that neurofilament degeneration was mediated primarily by NMDA receptor activity. This work suggests that excitotoxicity triggers a progressive pathway of cytoskeletal degeneration within axons, initially characterised by the loss of neurofilament proteins.
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