Neuronal networks provide rapid neuroprotection against spreading toxicity

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Samson, Andrew J. and Robertson, Graham and Zagnoni, Michele and Connolly, Christopher N. (2016) Neuronal networks provide rapid neuroprotection against spreading toxicity. Scientific Reports, 6. pp. 1-11. 33746. ISSN 2045-2322 (https://doi.org/10.1038/srep33746)

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Abstract

Acute secondary neuronal cell death, as seen in neurodegenerative disease, cerebral ischemia (stroke) and traumatic brain injury (TBI), drives spreading neurotoxicity into surrounding, undamaged, brain areas. This spreading toxicity occurs via two mechanisms, synaptic toxicity through hyperactivity, and excitotoxicity following the accumulation of extracellular glutamate. To date, there are no fast-acting therapeutic tools capable of terminating secondary spreading toxicity within a time frame relevant to the emergency treatment of stroke or TBI patients. Here, using hippocampal neurons (DIV 15-20) cultured in microfluidic devices in order to deliver a localized excitotoxic insult, we replicate secondary spreading toxicity and demonstrate that this process is driven by GluN2B receptors. In addition to the modeling of spreading toxicity, this approach has uncovered a previously unknown, fast acting, GluN2A-dependent neuroprotective signaling mechanism. This mechanism utilizes the innate capacity of surrounding neuronal networks to provide protection against both forms of spreading neuronal toxicity, synaptic hyperactivity and direct glutamate excitotoxicity. Importantly, network neuroprotection against spreading toxicity can be effectively stimulated after an excitotoxic insult has been delivered, and may identify a new therapeutic window to limit brain damage.

ORCID iDs

Samson, Andrew J., Robertson, Graham ORCID logoORCID: https://orcid.org/0000-0002-3841-874X, Zagnoni, Michele ORCID logoORCID: https://orcid.org/0000-0003-3198-9491 and Connolly, Christopher N.;
CORE (COnnecting REpositories)