Investigating the Role of Lactate in Regulating Gene Expression through Epigenetic Modifications in Neuronal Cells
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PhD Dissertation_Manar Darwish_Summer 2020.pdf
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PhD Dissertation
Type
DissertationAuthors
Darwish, Manar M.
Advisors
Magistretti, Pierre J.
Committee members
Merzaban, Jasmeen
Aranda, Manuel

Gräff, Johannes
Fiumelli, Hubert
Program
BioscienceKAUST Department
Biological and Environmental Science and Engineering (BESE) DivisionDate
2019-11Embargo End Date
2021-06-14Permanent link to this record
http://hdl.handle.net/10754/663537
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At the time of archiving, the student author of this dissertation opted to temporarily restrict access to it. The full text of this dissertation became available to the public after the expiration of the embargo on 2021-06-14.Abstract
Lactate has been long thought of as a dead-end waste product of glycolysis. In the brain, recent evidence has revealed a key role of L-lactate creating a paradigm-shift in our understanding of the neuronal energy metabolism. The Astrocyte neuron lactate shuttle (ANLS) model, has shown L-Lactate as the main energy substrate delivered by astrocytes to neurons to sustain neuronal oxidative metabolism. This metabolic coupling is an essential mechanism for long-term memory formation. Experimental evidence indicates that the role of lactate in cognitive function is not limited to being a neuronal metabolic substrate, but rather it is also an important signaling molecule for synaptic plasticity. One of the new emerging roles of lactate is its effect on gene expression levels; however, our current understanding of the mechanism of lactate effect on gene expression is rudimentary. Here, I investigate the role of lactate as an epigenetic modulator in neuronal cultures. First, I explored the effect of lactate on the transcriptome and methylome of the neuronal cells using primary neuronal cell culture models. Our results reveal a significant role for lactate in inducing neuronal cell differentiation. Following, I characterized a neuroblastoma cell line as our neuronal differentiation cell model and assessed its metabolic features relative to other immortal cell lines. Further, using the cell line in vitro model, I looked into the metabolic reprograming that occurs in parallel with the first indications of differentiation, focusing on lactate production rates. Subsequently, I investigated the role of lactate in differentiation through transcriptomic analysis. We show that lactate induced histone acetylation and promoted expression of dopaminergic markers, with a stronger effect of D-lactate over L-lactate. Further studies to establish potential linkages between those two pathways will enhance our understanding of the effect of lactate.Citation
Darwish, M. M. (2019). Investigating the Role of Lactate in Regulating Gene Expression through Epigenetic Modifications in Neuronal Cells. KAUST Research Repository. https://doi.org/10.25781/KAUST-R9451ae974a485f413a2113503eed53cd6c53
10.25781/KAUST-R9451