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Burton, S.

Publications and source records attributed to Burton, S..

3 recordsLinked to original sources

Dissecting novel object exploration: a fully automated homecage-based novel object recognition test

The novel object recognition test is a frequently used memory test in rodents. Due to its ethological nature, cross-species relevance, and specificity to testing hippocampal and parahippocampal function, it has been widely applied in basic and translational research. However, its implementation proves challenging due to multiple uncontrolled factors. Here, we describe a fully automated homecage-based novel object recognition test for assessing long-term object memory in mice. We present an empirically guided computational model to show the robustness of this approach despite ambiguity in defining exploratory behaviours. We show that mice preferentially explored novel compared to familiar objects after 24-hour and 7-day retention periods, starting to discern them while still a distance away. The findings were replicated across two facilities. Furthermore, the ability to recognise the novel object depends on the mouses prior interactions with the replaced object after 24 hours, but not after 7 days. Finally, we showed that external factors may introduce undesired exploration biases, which can be addressed using relative instead of absolute discrimination measures. The fully automated homecage-based object recognition test will improve standardisation, rigour, and reproducibility, as well as expand our understanding of the factors influencing object exploratory behaviours and object memory. MotivationRecognition of objects as novel or familiar is an important cognitive memory function with cross-species relevance. Extensive work has provided a good understanding of the brain regions involved. Despite the apparent simplicity of novel object recognition (NOR) tests, they remain challenging due to their sensitivity to various uncontrolled experimental factors and differences in study design. Here, we report a fully automated standardised NOR test carried out in a mouses homecage, which minimises previously reported variability in NOR tests. HighlightsO_LIFully automated novel object recognition test for assessing long-term object memory in the mouses homecage C_LIO_LIA robust analysis pipeline described C_LIO_LITest replicated in two facilities with comparable results C_LIO_LIAn empirically guided computational model pointing to the robustness of this approach introduced C_LIO_LIMajor factors affecting the ability to discriminate novel from familiar objects, including object exploration bias, are described C_LI

neuroscience↗

Poldip2 deficiency attenuates disease severity in a mouse model of COVID-19

The lungs are the primary target of severe acute respiratory syndrome coronavirus 2 (SARS-CoV- 2), with the infection resulting in lung inflammation, pulmonary vascular leakage and diffuse alveolar damage. Polymerase delta-interacting protein-2 (Poldip2) mediates lung inflammation and vascular permeability after lipopolysaccharide-induced acute respiratory distress syndrome; however, its role in regulating lung permeability, vascular inflammation and tissue damage following SARS-CoV-2 infection is completely unknown. Here, we assessed the role of Poldip2 in inflammation, immune cell infiltration and lung tissue damage in response to SARS-CoV-2 infection. Our data shows that while deletion of Poldip2 does not affect the susceptibility to SARS- CoV-2 infection, mice heterozygous for Poldip2 exhibit reduced lung tissue damage, reduced cytokine and chemokine induction and decreased infiltration of myeloperoxidase (MPO)-positive neutrophils into inflamed lung tissue. These data reveal that Poldip2 depletion mitigates inflammation and immune cell infiltration following SARS-CoV-2 infection, highlighting the therapeutic potential of Poldip2 inhibition to attenuate severe lung injury.

pathology↗

Simultaneous representation of multiple time horizons by entorhinal grid cells and CA1 place cells

Grid cells and place cells constitute the basic building blocks of the medial entorhinal-hippocampal spatial cognitive map by representing the spatiotemporal continuum of an animals past, present and future locations. However, the spatiotemporal relationship between these different cell types is unclear. Here we co-recorded grid and place cells in freely foraging rats. We show that average time shifts in grid cells tend to be prospective and are proportional to their spatial scale, providing a nearly instantaneous readout of a spectrum of progressively increasing time horizons ranging hundreds of milliseconds. Average time shifts of place cells are generally larger compared to grid cells and also increase with place field sizes. Moreover, time shifts displayed nonlinear modulation by the animals trajectories in relation to the local boundaries and locomotion cues. Finally, long and short time shifts occurred at different parts of the theta cycle, which may facilitate their readout. Together, these findings suggest that progressively increasing time horizons of grid and place cells may provide a basis for calculating animal trajectories essential for goal-directed navigation and planning.

neuroscience↗