Abstract
Several “low molecular weight” or “secretory” phospholipases A2 isoforms may be expressed in mammalian neural cells. Indeed, mRNAs for GIB, GIIA, GIIE, GIII, GV, GX, and GXII were detected in brain tissues despite different levels. However, only the presence of GIB, GIIA, and GV proteins has been clearly demonstrated in neural cells or in the nervous tissue. Although the roles of GIB and GV in the nervous tissue are still elusive, there is evidence to support the involvement of GIIA in physiological and pathological events, including neurotransmission, long-term potentiation, and neuritogenesis. The neurotoxic effects of an increase in GIIA may be envisaged under pathological conditions associated with the activation of astrocytes during inflammation or through activation of neurons and enzymes due to the stimulation of the NMDA glutamate receptor. In the past, elevation of GIIA expression in many acute and chronic neurological diseases is well known. Although each neurodegenerative disease has a separate etiology, many share similar neurochemical common processes, such as excitotoxicity, oxidative stress, and mitochondrial dysfunction, phenomena where GIIA play an important role.
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Acknowledgements
This work was supported by a grant (2008.0.21.321) from Fondazione Cassa di Risparmio di Perugia. We thank Prof. Ildo Nicoletti (Laboratory of Image Analysis, University of Perugia) and Prof. Rosario Donato (Department of Experimental Medicine and Biochemical Sciences, University of Perugia) for the confocal immunofluorescence analysis.
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Dedicated to Prof. Lloyd A. Horrocks
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Goracci, G., Ferrini, M. & Nardicchi, V. Low Molecular Weight Phospholipases A2 in Mammalian Brain and Neural Cells: Roles in Functions and Dysfunctions. Mol Neurobiol 41, 274–289 (2010). https://doi.org/10.1007/s12035-010-8108-6
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DOI: https://doi.org/10.1007/s12035-010-8108-6