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Cabezas-Wallscheid, N.

Publications and source records attributed to Cabezas-Wallscheid, N..

2 recordsLinked to original sources

Gene expression noise dynamics unveil functional heterogeneity of ageing hematopoietic stem cells

Variability of gene expression due to stochasticity of transcription or variation of extrinsic signals, termed biological noise, is a potential driving force of cellular differentiation. While unicellular organisms exploit noise as a bet-hedging strategy, its role during multilineage differentiation of stem cells is underexplored. Utilizing single-cell RNA-sequencing to reconstruct cell state manifolds, we developed VarID2, a method for the quantification of biological noise at single-cell resolution. VarID2 reveals enhanced nuclear versus cytoplasmic noise across cell types of the peripheral blood, and distinct regulatory modes stratified by correlation between noise, expression, and chromatin accessibility. Noise levels are minimal in murine hematopoietic stem cells and increase during both differentiation and ageing. Differential noise identified myeloid-biased Dlk1+ long-term-HSCs in aged mice with enhanced quiescence and self-renewal capacity. VarID2 reveals fundamental properties of noise across cellular compartments, during stem cell differentiation and ageing, and uncovers distinct cellular sub-states invisible to conventional gene expression analysis.

systems biology↗

Prenatal inflammation perturbs fetal hematopoietic development and causes persistent changes to postnatal immunity

Adult hematopoietic stem and progenitor cells (HSPCs) respond directly to inflammation and infection, resulting in both acute and persistent changes to quiescence, mobilization, and differentiation. Here we show that fetal HSPCs respond to prenatal inflammation in utero, and that the fetal response shapes postnatal hematopoiesis and immunity. Heterogenous fetal HSPCs showed divergent responses to maternal immune activation (MIA), including changes in quiescence, expansion, and lineage-biased output. Single cell transcriptomic analysis of fetal HSPCs in response to MIA revealed specific upregulation of inflammatory gene profiles in discrete, transient HSC populations, that propagated expansion of lymphoid-biased progenitors. Beyond fetal development, MIA caused the inappropriate expansion and persistence of fetal lymphoid-biased progenitors postnatally, concomitant with increased cellularity and hyperresponsiveness of fetal-derived innate-like lymphocytes. Our investigation demonstrates how inflammation in utero can direct the trajectory of output and function of fetal-derived immune cells by reshaping fetal HSC establishment.

cell biology↗