Portrait of Chloé Savignac is unavailable

Chloé Savignac

PhD - McGill University
Supervisor
Research Topics
Computational Biology
Computational Neuroscience
Medical Machine Learning

Publications

Cell type transcriptomic modules reveal shared molecular mechanisms in Alzheimer’s and Parkinson’s disease
Edward A. Fon
Alain Dagher
Yasser Iturria-Medina
Jo Anne Stratton
L. M. Hodgson
David A Bennett
Historically, Alzheimer's disease (AD) and Parkinson's disease (PD) have been investigated as two distinct disorders of the brain. However, … (see more)a few similarities in neuropathology and clinical symptoms have been documented over the years. Traditional single-gene centric studies, such as differential gene expression analyses, have struggled to unravel the molecular basis for the observed pathological links between AD and PD. To address this, we tailor a latent factor framework to analyze synchronous gene co-expression at sub-cell-type resolution. Utilizing large, single-nucleus transcriptomics datasets in AD (70,634 nuclei) and PD (340,902 nuclei) from postmortem human brains, we systematically extract and juxtapose disease-critical molecular signatures in the brain. Our transcriptomic analysis reveals shared molecular programs between AD and PD that systematically localize to specific glial and neuronal cell types. In neurons, convergent gene groups in AD and PD relate to cytoskeletal dynamics and mitochondrial stress mechanisms. Similarly, overlapping gene groups in microglia modules implicate T cell activation mechanisms and synapse pruning pathways. In parallel, AD- and PD-associated genes in astrocytes are involved in heavy metal processing; oligodendrocytes highlight convergent dysregulation in myelin synthesis. In addition, our analysis reveals APOE, an AD GWAS gene, has disease predictive roles in PD-associated gene modules. Conversely, SNCA, a PD GWAS gene, emerges within AD associated gene modules. Our multi-module sub-cell-type approach offers unique insights into the molecular basis of shared neuropathology in AD and PD.
Profiling the Cell-Type Specific Effects of Psilocybin in Medial Prefrontal Cortexh
Heike Schuler
Delong Zhou
Vedrana Cvetkovska
Yiu-Chung Tse
Juliet Meccia
Rosemary C. Bagot
Mitochondria‐nucleus crosstalk characterizes Alzheimer's disease across 1,5 million brain cells
Emerging insight from stem cell research reinforces Alzheimer's disease (AD) to affect mitochondrial protein expression. Compelling new evid… (see more)ence points to mitochondrial reactive oxygen species (ROS) as potential driving player in Aβ toxicity, mediated through glial cells and ultimately impacting neuronal health. A comprehensive understanding of how oxidative phosphorylation variations relate to cell function remains largely unexplored, especially through a cell type lens. Leveraging today's largest single‐nucleus RNA sequencing dataset of AD, we unveil how cell‐type‐specific mitochondrial alterations reverberate in the nuclear transcriptome, in 424 AD patients and healthy controls from ROSMAP. By adopting a supervised latent factor modelling approach, we identified distinct gene modules capturing unique aspects of the mitochondrial crosstalk in 6 major brain cell types across 5,427 nuclear and 13 mitochondrial genes. We found that nuclear‐mitochondrial crosstalk varies distinctly with cell identity, reflecting metabolic demands and functional specialization. In neurons and oligodendrocytes, ATP synthase (complex V) takes a central role, whereas type 1 NADH dehydrogenase (complex I) is more prominent in astrocytes, microglia, and OPCs. Screening across >1 million gene expression profiles from ∼20,000 drug perturbations identified mitochondrial‐nuclear signatures that resemble those activated by parthenolide and niclosamide—two chemical compounds previously associated with oxidative stress and cytotoxicity via ubiquitination—as most predictive of AD. Microglia and OPCs achieved the highest overall classification accuracy, with stronger predictive performance observed in males than in females. Mapping gene module expressions to the Allen Human Brain Atlas revealed shared whole‐brain patterns highlighting the precuneus, which we implicated in ubiquitin‐cascade‐enriched modules. Clinical phenotyping revealed that males with higher AD risk, as indicated by their mitochondrial‐nuclear scores on glial gene modules, exhibited a greater pathological burden, including higher amyloid load, Parkinson's‐like symptoms, and neuroticism‐related traits. Finally, by comparing our findings with 2.5 million CRISPRi‐based perturbations, we identified neural signatures associated with female‐biased transcription factors and fatty acid biosynthesis, while glial signatures were linked to DNA damage and oxidative stress. By integrating multiple layers of biological data from established reference atlases, our analysis of mitochondria‐nuclear crosstalk revealed distinct transcriptional signatures associated with AD risk in glial and neural cells, with these associations exhibiting sex‐biased patterns.
Cell-type specific transcriptional modulation by psilocybin induces sustained plasticity in mouse medial prefrontal cortex
Heike Schuler
Delong Zhou
Vedrana Cvetkovska
Yiu-Chung Tse
Juliet Meccia
Joëlle Lopez
Ashot S. Harutyunyan
Jiannis Ragoussis
Rosemary C. Bagot
Despite enormous interest in psychedelics for psychiatric interventions, potential underlying biological mechanisms remain unclear. Here, we… (see more) confirm that a single dose of psilocybin increases synaptic transmission in mouse medial prefrontal cortex. Using scRNA-sequencing, we identify cell-type specific mechanisms of sustained neuroplastic effects. We show that, 24h post-psilocybin, expression of plasticity-related genes is increased in excitatory neurons and that transcription in a type of deep layer near projecting neuron, L5/6 NP, is robustly altered. Analyzing receptor expression patterns reveals that this cell-type specificity does not align with 5-HT 2A expression but aligns with 5-HT 2C expression patterns. Further, multivariate analyses identify psilocybin-induced gene expression patterns in L5/6 NP neurons predict 5-HT 2C , but not 5-HT 2A , transcript levels. Pharmacologic manipulation with a 5-HT 2C antagonist attenuates the post-acute sustained effect of psilocybin on synaptic transmission, highlighting 5-HT 2C signaling and L5/6 NP neurons as key mediators of psychedelic drug action’s sustained neuroplastic effects in mPFC.
Recovering undersampled single-cell transcriptomes with HyperCell
Abstract

Single-cell transcriptomic technology has now matured, allowing quantification of mRNA transcripts corres… (see more)ponding to tens of thousands of genes within a cell. However, still only a small fraction of these mRNA is captured and measured by today’s single-cell assays. There are likely hundreds of thousands of mRNA copies present within a typical human cell, yet these assays omit a majority of the transcripts that are actually present. This introduces technical noise, especially non-biological variability and excessive sparsity, which frustrates downstream analysis and potentially skews biological conclusions. To overcome these challenges, we here develop HyperCell, a probabilistic deep learning approach that explicitly models this undersampling to produce estimates of each cell’s original gene transcript abundances across the whole transcriptome. We demonstrate that our framework offers benefits in various mRNA modeling settings, by i) correctly differentiating between spurious sampling-induced and real biological zeros, outperforming existing approaches, ii) estimating the total mRNA content of cells across states to reduce contamination due to background transcripts, iii) reducing contamination due to background transcripts, and iv) helping to counteract biases that may appear during typical differential gene expression analyses using widespread normalization approaches. Our approach to correcting for the technical noise introduced by the single-cell experimental process brings us closer to studying biology, starting from the true transcriptome of cells.

Cell type transcriptomics reveal shared genetic mechanisms in Alzheimer’s and Parkinson’s disease
Edward A. Fon
Alain Dagher
Yasser Iturria-Medina
Jo Anne Stratton
David A Bennett
Historically, Alzheimer’s disease (AD) and Parkinson’s disease (PD) have been investigated as two distinct disorders of the brain. Howev… (see more)er, a few similarities in neuropathology and clinical symptoms have been documented over the years. Traditional single gene-centric genetic studies, including GWAS and differential gene expression analyses, have struggled to unravel the molecular links between AD and PD. To address this, we tailor a pattern-learning framework to analyze synchronous gene co-expression at sub-cell-type resolution. Utilizing recently published single-nucleus AD (70,634 nuclei) and PD (340,902 nuclei) datasets from postmortem human brains, we systematically extract and juxtapose disease-critical gene modules. Our findings reveal extensive molecular similarities between AD and PD gene cliques. In neurons, disrupted cytoskeletal dynamics and mitochondrial stress highlight convergence in key processes; glial modules share roles in T-cell activation, myelin synthesis, and synapse pruning. This multi-module sub-cell-type approach offers insights into the molecular basis of shared neuropathology in AD and PD.
Cell type transcriptomics reveal shared genetic mechanisms in Alzheimer’s and Parkinson’s disease
Edward A. Fon
Alain Dagher
Yasser Iturria-Medina
Jo Anne Stratton
David A Bennett
Historically, Alzheimer’s disease (AD) and Parkinson’s disease (PD) have been investigated as two distinct disorders of the brain. Howev… (see more)er, a few similarities in neuropathology and clinical symptoms have been documented over the years. Traditional single gene-centric genetic studies, including GWAS and differential gene expression analyses, have struggled to unravel the molecular links between AD and PD. To address this, we tailor a pattern-learning framework to analyze synchronous gene co-expression at sub-cell-type resolution. Utilizing recently published single-nucleus AD (70,634 nuclei) and PD (340,902 nuclei) datasets from postmortem human brains, we systematically extract and juxtapose disease-critical gene modules. Our findings reveal extensive molecular similarities between AD and PD gene cliques. In neurons, disrupted cytoskeletal dynamics and mitochondrial stress highlight convergence in key processes; glial modules share roles in T-cell activation, myelin synthesis, and synapse pruning. This multi-module sub-cell-type approach offers insights into the molecular basis of shared neuropathology in AD and PD.
Large language models auto-profile conscious awareness changes under psychedelic drug effects
Robin Carhart-Harris
Steven Laureys
Abstract

Psychedelic experiences open a colorful view into drug-induced changes in conscious awareness. Small-samp… (see more)le studies on psychedelic drug action have gained traction in recent years. Yet, today’s means for measuring changes in subjective experience are mostly limited to legacy questionnaires of pre-assumed relevance, which could be complemented by bottom-up explorations of semantic facets that underlie experience reports. Here, we show how to harness large language models (LLMs) to i) design from scratch, ii) annotate at scale, and iii) evaluate with rigor a vast portfolio of experience dimensions during psychoactive drug influence, yielding > 2 million automatic dimension ratings that would otherwise have been done by hand. Investigator-independent LLM scoring of these drug effects on the human mind alone allowed to robustly discriminate the unique mental effects of 30 psychoactive substances. Successful knowledge integration of how psychedelics mediate shifts in subjective awareness will be an unavoidable milestone towards charting the full drug design space.

Dissociable influences of maternal vs paternal Alzheimer’s risk on neurocognitive and cardiovascular health in men and women
Frederic St‐Onge
Sylvia Villeneuve
AmanPreet Badhwar
Sarah A Gagliano Taliun
Sali Farhan
Maiya R. Geddes
Yasser Iturria Medina
Judes Poirier
R. Nathan Spreng
We uncovered IPs of AD susceptibility differently expressed in male and female probands and affected by the diagnosed parent’s sex. Matern… (see more)al inheritance highlighted memory performance in both sexes, whereas paternal inheritance was particularly linked to cardiovascular health in males. The inheritance of the IPs was reflected in the brain structure at both superficial and deeper layers of the cortex. As the first study of its kind, our cross‐generational analysis of matri‐ vs. patrilinear AD risk bridges the epidemiological and clinical literature by leveraging the power of ∼1,000 patient visits. Our completely data‐driven framework ultimately dissociated phenotypes of maternal and paternal AD risk single‐handedly expressed in male and female probands.
APOE alleles are associated with sex-specific structural differences in brain regions affected in Alzheimer's disease and related dementia
Sylvia Villeneuve
AmanPreet Badhwar
Kimia Shafighi
Chris Zajner
Vaibhav Sharma
Sarah A. Gagliano Taliun
Sali Farhan
Judes Poirier
Alzheimer’s disease is marked by intracellular tau aggregates in the medial temporal lobe (MTL) and extracellular amyloid aggregates in th… (see more)e default network (DN). Here, we examined codependent structural variations between the MTL’s most vulnerable structure, the hippocampus (HC), and the DN at subregion resolution in individuals with Alzheimer’s disease and related dementia (ADRD). By leveraging the power of the approximately 40,000 participants of the UK Biobank cohort, we assessed impacts from the protective APOE ɛ2 and the deleterious APOE ɛ4 Alzheimer’s disease alleles on these structural relationships. We demonstrate ɛ2 and ɛ4 genotype effects on the inter-individual expression of HC-DN co-variation structural patterns at the population level. Across these HC-DN signatures, recurrent deviations in the CA1, CA2/3, molecular layer, fornix’s fimbria, and their cortical partners related to ADRD risk. Analyses of the rich phenotypic profiles in the UK Biobank cohort further revealed male-specific HC-DN associations with air pollution and female-specific associations with cardiovascular traits. We also showed that APOE ɛ2/2 interacts preferentially with HC-DN co-variation patterns in estimating social lifestyle in males and physical activity in females. Our structural, genetic, and phenotypic analyses in this large epidemiological cohort reinvigorate the often-neglected interplay between APOE ɛ2 dosage and sex and link APOE alleles to inter-individual brain structural differences indicative of ADRD familial risk.
<i>APOE</i> ɛ2 vs <i>APOE</i> ɛ4 dosage shows sex-specific links to hippocampus-default network subregion co-variation
Sylvia Villeneuve
AmanPreet Badhwar
Kimia Shafighi
Chris Zajner
Vaibhav Sharma
Sarah A Gagliano Taliun
Sali Farhan
Judes Poirier
Alzheimer’s disease and related dementias (ADRD) are marked by intracellular tau aggregates in the medial-temporal lobe (MTL) and extracel… (see more)lular amyloid aggregates in the default network (DN). Here, we sought to clarify ADRD-related co-dependencies between the MTL’s most vulnerable structure, the hippocampus (HC), and the highly associative DN at a subregion resolution. We confronted the effects of APOE ɛ2 and ɛ4, rarely investigated together, with their impact on HC-DN co-variation regimes at the population level. In a two-pronged decomposition of structural brain scans from ∼40,000 UK Biobank participants, we located co-deviating structural patterns in HC and DN subregions as a function of ADRD family risk. Across the disclosed HC-DN signatures, recurrent deviations in the CA1, CA2/3, molecular layer, fornix’s fimbria, and their cortical partners related to ADRD risk. Phenome-wide profiling of HC-DN co- variation expressions from these population signatures revealed male-specific associations with air-pollution, and female-specific associations with cardiovascular traits. We highlighted three main factors associated with brain-APOE associations across the different gene variants: happiness, and satisfaction with friendships, and with family. We further showed that APOE ɛ2/2 interacts preferentially with HC-DN co-variation patterns in estimating social lifestyle in males and physical activity in females. Our findings reinvigorate the often-neglected interplay between APOE ɛ2 dosage and sex, which we have linked to fine-grained structural divergences indicative of ADRD susceptibility.