The mitochondrial calcium uniporter is crucial for the generation of fast cortical network rhythms

Author:

Bas-Orth Carlos123,Schneider Justus34,Lewen Andrea34,McQueen Jamie56,Hasenpusch-Theil Kerstin6,Theil Thomas6,Hardingham Giles E56,Bading Hilmar13,Kann Oliver34ORCID

Affiliation:

1. Department of Neurobiology, University of Heidelberg, Heidelberg, Germany

2. Institute of Anatomy and Cell Biology, University of Heidelberg, Heidelberg, Germany

3. Interdisciplinary Center for Neurosciences (IZN), University of Heidelberg, Heidelberg, Germany

4. Institute of Physiology and Pathophysiology, University of Heidelberg, Heidelberg, Germany

5. UK Dementia Research Institute, University of Edinburgh, Edinburgh, UK

6. Centre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK

Abstract

The role of the mitochondrial calcium uniporter (MCU) gene ( Mcu) in cellular energy homeostasis and generation of electrical brain rhythms is widely unknown. We investigated this issue in mice and rats using Mcu-knockout and -knockdown strategies in vivo and in situ and determined the effects of these genetic manipulations on hippocampal gamma oscillations (30–70 Hz) and sharp wave-ripples. These physiological network states require precise neurotransmission between pyramidal cells and inhibitory interneurons, support spike-timing and synaptic plasticity and are associated with perception, attention and memory. Absence of the MCU resulted in (i) gamma oscillations with decreased power (by >40%) and lower synchrony, including less precise neural action potential generation (‘spiking'), (ii) sharp waves with decreased incidence (by about 22%) and decreased fast ripple frequency (by about 3%) and (iii) lack of activity-dependent pyruvate dehydrogenase dephosphorylation. However, compensatory adaptation in gene expression related to mitochondrial function and glucose metabolism was not detected. These data suggest that the neuronal MCU is crucial for the generation of network rhythms, most likely by influences on oxidative phosphorylation and perhaps by controlling cytoplasmic Ca2+ homeostasis. This work contributes to an increased understanding of mitochondrial Ca2+ uptake in cortical information processing underlying cognition and behaviour.

Publisher

SAGE Publications

Subject

Cardiology and Cardiovascular Medicine,Neurology (clinical),Neurology

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