Curcio, M., Salazar, I.L., Mele, M., Canzoniero, L.M.T., Duarte, C.B.
Calpains and neuronal damage in the ischemic brain: The swiss knife in synaptic injury
(2016) Progress in Neurobiology, 143, pp. 1-35.
https://www.scopus.com/inward/record.uri?eid=2-s2.0-84979684030&partnerID=40&md5=19a8615887ad35ddb4085a6682819135
DOI: 10.1016/j.pneurobio.2016.06.001
AFFILIATIONS: CNC – Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal;
Doctoral Programme in Experimental Biology and Biomedicine, Center for Neuroscience and Cell Biology, University of Coimbra, 3004-504, Coimbra, Portugal, Institute for Interdisciplinary Research, University of Coimbra (IIIUC), Coimbra, Portugal;
Department of Science and Technology, University of Sannio, Benevento, Italy;
Department of Life Sciences, University of Coimbra, Coimbra, Portugal
ABSTRACT: The excessive extracellular accumulation of glutamate in the ischemic brain leads to an overactivation of glutamate receptors with consequent excitotoxic neuronal death. Neuronal demise is largely due to a sustained activation of NMDA receptors for glutamate, with a consequent increase in the intracellular Ca2+ concentration and activation of calcium- dependent mechanisms. Calpains are a group of Ca2+-dependent proteases that truncate specific proteins, and some of the cleavage products remain in the cell, although with a distinct function. Numerous studies have shown pre- and post-synaptic effects of calpains on glutamatergic and GABAergic synapses, targeting membrane- associated proteins as well as intracellular proteins. The resulting changes in the presynaptic proteome alter neurotransmitter release, while the cleavage of postsynaptic proteins affects directly or indirectly the activity of neurotransmitter receptors and downstream mechanisms. These alterations also disturb the balance between excitatory and inhibitory neurotransmission in the brain, with an impact in neuronal demise. In this review we discuss the evidence pointing to a role for calpains in the dysregulation of excitatory and inhibitory synapses in brain ischemia, at the pre- and post-synaptic levels, as well as the functional consequences. Although targeting calpain-dependent mechanisms may constitute a good therapeutic approach for stroke, specific strategies should be developed to avoid non-specific effects given the important regulatory role played by these proteases under normal physiological conditions. © 2016 Elsevier Ltd
CORRESPONDENCE ADDRESS: Duarte, C.B.; Center for Neuroscience and Cell Biology, University of CoimbraPortugal; email: cbduarte@ci.uc.pt
