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University of Cambridge > Talks.cam > MRC Mitochondrial Biology Unit Seminars > Mitochondrial dysfunction and signalling in the nervous system
Mitochondrial dysfunction and signalling in the nervous systemAdd to your list(s) Download to your calendar using vCal
If you have a question about this talk, please contact hkb33. The overall goal of our work is to understand the effects of mitochondrial dysfunction in the nervous system and how this contributes to neurodegeneration. Mitochondria are abundant in almost every cell type and are particularly important in the nervous system. Mitochondria generate the majority of cellular ATP but also metabolize fatty acids, synthesize amino acids, buffer cellular calcium ions, produce reactive oxygen species, synthesise iron-sulphur clusters and mediate programmed cell death. Altered mitochondrial activity or mitochondrial dysfunction causes ‘mitochondrial retrograde signalling’ pathways to be activated, resulting in altered nuclear gene expression. To study mitochondrial retrograde signalling in the nervous system we have developed Drosophila models of neuronal specific mitochondrial dysfunction. I will discuss our recent work where we have shown that mitochondrial dysfunction activates endoplasmic reticulum stress signalling in neurons. We have furthermore used transcriptomics and metabolomics to identify a novel mechanism, triggered by mitochondrial dysfunction and endoplasmic reticulum stress signalling, which contributes to loss of neuronal function in Drosophila. This mechanism may be relevant to mitochondrial disease and neurodegenerative diseases associated with mitochondrial dysfunction. This talk is part of the MRC Mitochondrial Biology Unit Seminars series. This talk is included in these lists:
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