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Zoodsma, M.

Publications and source records attributed to Zoodsma, M..

3 recordsLinked to original sources

Integrative transcriptomics and electrophysiological profiling of hiPSC-derived neurons identifies novel druggable pathways in Koolen-de Vries Syndrome

Koolen-de Vries Syndrome (KdVS) is a neurodevelopmental disorder (NDD) with no treatment options due to a lack of understanding of its underlying pathophysiology. To investigate neuronal activity in KdVS, human induced pluripotent stem cell (hiPSC)-derived neurons from KdVS and control subjects were cultured on microelectrode arrays (MEAs). Our study identified reduced network burst rates, indicating disorganized network activity in KdVS neurons. To bridge molecular and functional aspects of the syndrome, we developed an experimental framework, MEA-seq, that integrates network activity measurements with high-throughput transcriptome profiling. This approach identified a negative correlation between the expression of the NDD-associated gene CLCN4 and the network burst rate. Consequently, knockdown of CLCN4 in KdVS neurons restored the activity to control level, confirming a causal relationship between increased CLCN4 expression and reduced network burst rate. Additionally, we identified a positive correlation between mitochondrial gene expression and the network burst rate, and identified impaired mitochondrial function in KdVS hiPSC-derived neurons. The transcriptomic signature of KdVS neurons was then used for computational screening against drug perturbation signatures of the LINCS Consortium database, predicting other drug targets and compounds capable of reversing the expression of affected genes in KdVS neurons. We selected 10 compounds for experimental validation, identifying the antioxidant phloretin and the Rho-kinase inhibitor fasudil as potential candidates for restoring the network activity dysfunction in KdVS. We conclude that the integrative molecular and electrophysiological of hiPSC-derived neurons with MEA-seq has excellent potential for identifying novel drugs and druggable pathways for KdVS and other NDDs.

neuroscience↗

CellDemux: coherent genetic demultiplexing in single-cell and single-nuclei experiments.

Multiplexed single-cell experiment designs are superior in terms of reduced batch effects, increased cost-effectiveness, throughput and statistical power. However, current computational strategies using genetics to demultiplex single-cell (sc) libraries are limited when applied to single-nuclei (sn) sequencing data (e.g., snATAC-seq and snMultiome). Here, we present CellDemux: a computational framework for genetic demultiplexing within and across data modalities, including single-cell, single-nuclei and paired snMultiome measurements. CellDemux uses a consensus approach, leveraging modality-specific tools to robustly identify non-empty oil droplets and singlets, which are subsequently demultiplexed to donors. Notable, CellDemux demonstrates good performance in demultiplexing snMultiome data and is generalizable to single modalities, i.e. snATAC-seq and sc/snRNA-seq libraries. We benchmark CellDemux on 187 genetically multiplexed libraries from 800 samples (scRNA-seq, snATAC-seq, CITE-seq and snMultiome), confidently identifying and assigning cells to 88% of donors. In paired snMultiome libraries, CellDemux achieves consistent demultiplexing across data modalities. Moreover, analysis of 38 snATAC libraries from 149 samples shows that CellDemux retains more genetically demultiplexed nuclei for downstream analyses compared to existing methods. In summary, CellDemux is a modular and robust framework that deconvolves donors from genetically multiplexed single-cell and single-nuclei RNA/ATAC/Multiome libraries.

genomics↗

Differences in anti-viral immune responses in individuals of Indian and European origin: relevance for the COVID-19 pandemic

During the COVID-19 pandemic, large differences in susceptibility and mortality due to SARS-CoV-2 infection have been reported between populations in Europe and South Asia. While both host and environmental factors (including BCG vaccination) have been proposed to explain this, the potential biological substrate of these differences is unknown. We purified peripheral blood mononuclear cells from individuals living in India and the Netherlands at baseline and 10-12 weeks after BCG vaccination. We compared chromatin accessibility between the two populations at baseline, as well as gene transcription profiles and cytokine production capacities upon viral stimulation with influenza and SARS-CoV-2. The chromatin accessibility of genes important for adaptive immunity was higher in Indians compared to Europeans, while the latter had more accessible chromatin regions in genes of the innate immune system. At the transcriptional level, we observed that Indian volunteers displayed a more tolerant immune response to viral stimulation, in contrast to a more exaggerated response in Europeans. BCG vaccination strengthened the tolerance program in Indians, but not in Europeans. These differences may partly explain the different impact of COVID-19 on the two populations.

immunology↗