Expression of the calcium-binding protein, parvalbumin, in cultured cortical neurons using a HSV-1 vector system enhances NMDA neurotoxicity.

Abstract

Calcium-binding proteins (CaBPs) are a family of proteins having a unique distribution in the brain and are thought to be important in buffering intracellular calcium. Glutamate neurotoxicity is a process by which the over-activation of glutamate receptors can cause the influx of excessive extracellular calcium and neuronal cell death. It has been proposed that neurons containing CaBP may be more resistant to glutamate neurotoxicity due to their increased ability to buffer calcium. Using a herpes simplex virus-1 (HSV-1) vector system we packaged the CaBP gene, parvalbumin, or the marker gene, beta-galactosidase (beta-gal), correctly in viron particles, which were found upon infection to express mRNA specific to these vectors. PC12 and neocortical cultures showed strong immunohistochemical staining for either beta-gal or parv. The cortical cultures stained positively for endogenous glutamate decarboxylase, a marker for GABAergic neurons, but not for endogenous parvalbumin, indicating that parvalbumin was being expressed ectopically from the HSV-1 vector. Interestingly, the expression of parvalbumin increased cortical culture's susceptibility to N-methyl-D-aspartate-induced neurotoxicity. This increase in neurotoxicity was not due to the wild-type virus or the helper virus which accompanies the packaging of these vectors. We speculate that the ectopic expression of parvalbumin in cortical cultures may be increasing glutamate release which in turn increases cell death.

• Authors: D M Hartley, R L Neve, J Bryan, D B Ullrey, S Y Bak, P Lang, A I Geller
• Journal: Brain research. Molecular brain research (Brain Res Mol Brain Res) Vol. 40 Issue 2 Pg. 285-96 (Sep 01 1996) ISSN: 0169-328X [Print] Netherlands
• PMID: 8872313 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)

Chemical References

• Parvalbumins
• N-Methylaspartate
• L-Lactate Dehydrogenase

Topics

• Animals
• Cells, Cultured (metabolism)
• Cerebral Cortex (metabolism)
• Dose-Response Relationship, Drug
• L-Lactate Dehydrogenase (metabolism)
• N-Methylaspartate (toxicity)
• PC12 Cells
• Parvalbumins (metabolism)
• Rats
• Simplexvirus