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Neuronal calcium dyshomeostasis as a crucial process in neuropath | 50266

Journal of Neurology & Neurophysiology

ISSN - 2155-9562

Neuronal calcium dyshomeostasis as a crucial process in neuropathologies

Joint Event on 23rd International Conference on Neurology & Neurophysiology & 24th International Conference on Neurosurgery and Neuroscience

March 18-19, 2019 Edinburgh, Scotland

Ludmila Zylinska, Bozena Ferenc and Tomasz Boczek

Medical University of Lodz, Poland
Stanford University School of Medicine, USA

Scientific Tracks Abstracts: J Neurol Neurophysiol

Abstract :

Oscillations of cytosolic Ca2+ are necessary for cellular signaling and propagation of Ca2+ signal is an absolute requirement for the functioning of neuronal cells. Ca2+ appears to be a universal and ubiquitous signaling molecule, thereby in resting neuronal cells its concentration is kept at ~100 nM against 1-2 mM outside the cell. Inability to maintain calcium homeostasis in neurons underlies many neuropathologies. Ca2+ may elicit a variety of different responses based on the type of targeted neurotransmission pathways, and it regulates synaptic plasticity, controls neuronal growth and neuronal survival. The plasma membrane contains a high affinity Ca2+-ATPase (PMCA) that translocates Ca2+ from the cytosol to the extracellular environment. The enzyme is coded by four separate genes (PMCA1-4), among which PMCA2 and PMCA3 are considered as neuron-specific forms. In the brain, PMCA function declines progressively during aging, thus impaired calcium homeostasis may contribute to neurodegeneration. We have developed the stable transfected differentiated PC12 cells with reduced level of PMCA2 or PMCA3, and the most critical finding was permanently increased resting Ca2+ concentration. Altered PMCA composition affected the expression level of several Ca2+-associated proteins (SERCA, calmodulin, calcineurin, neuromodulin) and certain types of voltage-gated calcium channels. We have also evidenced a novel PMCA role in regulation of bioenergetic pathways and mitochondrial activity. Interestingly, some changes could occur as adaptive processes protecting cells against calcium overload. Since age-related PMCA decrease has been documented, our modified PC12 cells may be a useful model to clarify the biological changes in neurons as well as to study the vulnerability of cells to neurodegenerative insults.

Biography :

Ludmila Zylinska PhD, DSc, is a Full Professor and Head of the Department of Molecular Neurochemistry, Medical University of Lodz, Poland. Her scientific interests are related to regulation of neuronal calcium homeostasis with particular attention brought on plasma membrane calcium pumps in the CNS, as well as on molecular mechanisms of calcium-dependent processes that regulate neuronal transmission in physiological and pathological conditions. She has published more than 60 papers in the areas of Biochemistry, Neuroscience and Cell Biology.

E-mail: ludmila.zylinska@umed.lodz.pl

 

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