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York, N. S.

Publications and source records attributed to York, N. S..

2 recordsLinked to original sources

Transient, early, female-specific increase in cortical glial fibrillary acidic protein distribution in the Syrian hamster model of mild peripheral COVID-19

BackgroundMild-moderate respiratory COVID-19 is commonly associated with a range of neurological symptoms. The mechanisms linking this peripheral disease to cognitive symptoms are thought to include heightened circulating cytokines and other inflammatory mediators resulting in a leaky blood-brain barrier and increased neuroinflammation (i.e., inflammation taking place in the brain). This can lead to aberrant synaptic transmission and cognitive dysfunction. A key component of neuroinflammation is the reactivity of astrocytes, in a process termed astrogliosis, associated with altered morphology, proliferative capacity, gene expression, and function. Accumulating evidence suggests astrogliosis likely occurs in mild-moderate COVID-19; however, there has been limited investigation. In this study, we quantified changes to astrocytes in a Syrian hamster model of mild-moderate respiratory COVID-19. MethodsWe used an intranasal inoculation model to produce mild-moderate respiratory COVID-19 in 8-10-week-old male and female Syrian hamsters. We extracted brains at 1-, 3-, 5-, 7-, and 31-days post-inoculation and from uninfected controls, and immunolabelled brain sections with astrocyte- (GFAP and SOX9) and neuron-specific (NEUN) markers. We captured tiled confocal micrographs of entire brain sections and analyzed the resulting signals from five regions of interest: cortex, corpus callosum, hippocampus, third ventricle, and dorsal striatum. ResultsTo systematically quantify cell-type-specific labelling for astrogliosis markers, we first developed an unbiased pipeline. We found a transient increase in GFAP signal density in female hamster, specifically in the cortex at 3 days post-inoculation. There were no corresponding changes noted in astrocyte (SOX9), neuron (NEUN) or total cell (Hoechst) numbers. Moreover, there were no changes in male hamsters at any timepoint in any region of interest. ConclusionsOur findings provide the first spatiotemporal insight into astrogliosis in a hamster model of mild-moderate respiratory COVID-19. We identified a transient and sex-specific increase in GFAP signal density, indicative of astrogliosis. Our findings contribute to the literature surrounding sex differences in (neuro)immune responses and add to the growing body of COVID-19 literature, in which sex-specific outcomes are apparent in both human patient populations and rodent experimental models.

neuroscience↗

Quantification of morphological, functional, and biochemical features of H9c2 rat cardiomyoblast retinoic acid differentiation

Cell culture models enable advancement in our understanding of heart development and heart disease. The H9c2 rat ventricular cardiomyoblast cell line can be differentiated, recapitulating certain components of cardiomyocyte development; however, morphological, functional, and biochemical changes are rarely investigated in parallel, thereby limiting fulsome understanding. We therefore characterized morphology, Ca2+ handling, and gene expression after five days (5 days-in-vitro, DIV5), and fourteen days (DIV14) of exposure to differentiation stimuli, consisting of retinoic acid and low serum. We observed several morphological changes with increasing time in differentiation, including increased mean length, area, eccentricity, and multinucleation, as well as an increase in actin clusters. Spontaneous Ca2+ transients in differentiated H9c2 cells had decreased frequency and synchronicity compared to those observed in primary cardiomyocytes. Additionally, key cardiomyocyte cytoskeletal proteins and ion channel transcript and protein expression levels changed significantly with differentiation, in alignment with changes normally observed in cardiomyocyte development. Our findings suggest H9c2 cells may be used as a high throughput screening model to investigate cardiomyocyte biology in certain developmental contexts with relevance to heart health and disease. HighlightsO_LIWe quantified morphology, Ca2+ handling, and gene expression changes in rat ventricular cardiomyoblast H9c2 cells across retinoic acid differentiation. C_LIO_LIWe compared multiple differentiation time points (mainly DIV0, DIV5, and DIV14) and observed time-dependent changes in all 3 aspects. We observed several morphological changes with increasing time in differentiation, including increased mean length, area, eccentricity, and multinucleation, as well as an increase in actin clusters. We observed the onset of spontaneous Ca2+ transients with differentiation, with further changes in subpopulations with increasing time in differentiation. Finally, we observed multiple changes in gene expression consistent with cardiomyocyte differentiation. C_LIO_LIWe summarize these parallel time-point dependent changes in morphology, Ca2+ handing, and gene expression to enable other researchers to optimize their study design. C_LI

cell biology↗