Literature DB >> 23142186

Over-expression of N-type calcium channels in cortical neurons from a mouse model of Amyotrophic Lateral Sclerosis.

Massimo Pieri1, Silvia Caioli, Nadia Canu, Nicola B Mercuri, Ezia Guatteo, Cristina Zona.   

Abstract

Voltage-gated Ca(2+) channels (VGCCs) mediate calcium entry into neuronal cells in response to membrane depolarisation and play an essential role in a variety of physiological processes. In Amyotrophic Lateral Sclerosis (ALS), a fatal neurodegenerative disease caused by motor neuron degeneration in the brain and spinal cord, intracellular calcium dysregulation has been shown, while no studies have been carried out on VGCCs. Here we show that the subtype N-type Ca(2+) channels are over expressed in G93A cultured cortical neurons and in motor cortex of G93A mice compared to Controls. In fact, by western blotting, immunocytochemical and electrophysiological experiments, we observe higher membrane expression of N-type Ca(2+) channels in G93A neurons compared to Controls. G93A cortical neurons filled with calcium-sensitive dye Fura-2, show a net calcium entry during membrane depolarization that is significantly higher compared to Control. Analysis of neuronal vitality following the exposure of neurons to a high K(+) concentration (25 mM, 5h), shows a significant reduction of G93A cellular survival compared to Controls. N-type channels are involved in the G93A higher mortality because ω-conotoxin GVIA (1 μM), which selectively blocks these channels, is able to abolish the higher G93A mortality when added to the external medium. These data provide robust evidence for an excess of N-type Ca(2+) expression in G93A cortical neurons which induces a higher mortality following membrane depolarization. These results may be central to the understanding of pathogenic pathways in ALS and provide novel molecular targets for the design of rational therapies for the ALS disorder.
Copyright © 2012 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Calcium current; Cortex; Electrophysiology; Fura-2; G93A

Mesh:

Substances:

Year:  2012        PMID: 23142186     DOI: 10.1016/j.expneurol.2012.11.002

Source DB:  PubMed          Journal:  Exp Neurol        ISSN: 0014-4886            Impact factor:   5.330


  10 in total

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Authors:  Mingchen C Jiang; Adesoji Adimula; Derin Birch; Charles J Heckman
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4.  Voltage-gated calcium channels are abnormal in cultured spinal motoneurons in the G93A-SOD1 transgenic mouse model of ALS.

Authors:  Qing Chang; Lee J Martin
Journal:  Neurobiol Dis       Date:  2016-05-02       Impact factor: 5.996

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7.  STIM1 Protein Activates Store-Operated Calcium Channels in Cellular Model of Huntington's Disease.

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Review 10.  Nearly 30 Years of Animal Models to Study Amyotrophic Lateral Sclerosis: A Historical Overview and Future Perspectives.

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  10 in total

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