Abstract
Annual Review of Pharmacology and Toxicology
Vol. 47:
117-141
(Volume publication date February 2007)
(doi:10.1146/annurev.pharmtox.47.120505.105311)
First published online as a Review in Advance on July 31, 2006Cell Signaling and Neuronal Death Makoto R. Hara1 and Solomon H. Snyder1,2,31The Solomon H. Snyder Department of Neuroscience, 2Department of Pharmacology and Molecular Science, and 3Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205; email: ssnyder@jhmi.edu, mhara@jhmi.edu Abstract The past few decades have revealed that cell death can be precisely programmed with two principal forms, apoptosis and necrosis. Besides pathophysiological alterations, physiologic processes, such as the pruning of neurons during normal development and the involution of the thymus, involve apoptosis. This review focuses on the role of inter- and intracellular signaling systems in cell death, especially in the nervous system. Among neurotransmitters, glutamate and nitric oxide have been most extensively characterized and contribute to cell death in excitotoxic damage, especially in stroke and possibly in neurodegenerative diseases. Within cells, calcium, the most prominent of all intracellular messengers, mediates diverse forms of cell death with actions modulated by many proteins, including IP3 receptors, calcineurin, calpain, and cytochrome c. Acronyms and Definitions Bcl-2 family: a family of proteins that regulate a critical intracellular checkpoint in the intrinsic pathway of apoptosis. They are usually categorized into different groups based on the presence of certain sequence motifs, Bcl-2 homology (BH) domains Glutamate carboxypeptidase II (GCPII): a metalloprotease that hydrolyses NAAG to N-actyl-L-aspartate (NAA). It also occurs in the prostate as prostate-specific membrane antigen (PSMA) and is released into the circulation in prostate cancer Inositol 1,4,5-trisphosphate (IP3): a second messenger that is produced primarily by phospholipase C (PLC) metabolism of phosphatidylinositol-4,5-bisphosphate (PIP2) in response to the stimulation of G protein–coupled receptors (GPCRs) or receptor tyrosine kinases (RTKs) Inositol 1,4,5-trisphosphate receptor (IP3R): receptors that release Ca2+ into the cytosol from internal stores in response to IP3 Ionotropic glutamate receptors: receptors that are also ion channels and pass electric current in response to gluamate binding Metabotropic glutamate receptors (mGluRs): seven transmembrane receptors that are coupled to second-messenger cascades via G-proteins N-acetyl-L-aspartyl-L-glutamate (NAAG): NAAG is one of the most prevalent neurotransmitters in the mammalian brain. NAAG acts as an agonist at Group II metabotropic glutamate receptors on neurons and glia S-nitrosylation: the coupling of an NO moiety to a cysteine thiol (-SH) to form an S-nitrosothiol (-SNO) Most recent citing papers (via CrossRef)Multiple Sklerose – eine Kanalopathie? Der Nervenarzt 80(4):422-429 (2009) Glutamate-induced post-activation inhibition of locus coeruleus neurons is mediated by AMPA/kainate receptors and sodium-dependent potassium currents British Journal of Pharmacology 156(4):649-661 (2009) Effect of radiofrequency electromagnetic field exposure on in vitro models of neurodegenerative disease Bioelectromagnetics:n/a-n/a (2009) Proteolytic fragments of laminin promote excitotoxic neurodegeneration by up-regulation of the KA1 subunit of the kainate receptor The Journal of Cell Biology 183(7):1299-1313 (2009) Oxidative impairment of hippocampal long-term potentiation involves activation of protein phosphatase 2A and is prevented by ketone bodies Journal of Neuroscience Research 86(15):3322-3330 (2008)
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