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Geurten, B. R. H.

Publications and source records attributed to Geurten, B. R. H..

3 recordsLinked to original sources

Axon demyelination and degeneration in a zebrafishspastizin model of hereditary spastic paraplegia

Hereditary spastic paraplegias (HSPs) are a diverse set of neurological disorders characterized by progressive spasticity and weakness in the lower limbs caused by damage to the axons of the corticospinal tract. More than 88 genetic mutations have been associated with HSP, yet the mechanisms underlying these disorders are little understood. We studied the pathogenesis of one form of HSP known as spastic paraplegia 15 (SPG15). This disorder is caused by mutations in the ZFYVE26 gene, which codes for a protein called SPASTIZIN. We show that, in zebrafish, the significant reduction of Spastizin caused degeneration of Mauthner (M)-cells. M-cell degeneration is associated with axon demyelination in the spinal cord and impaired locomotion in the spastizin mutants. Our findings reveal that the mutation not only compromises axonal integrity but also affects the structural molecules of the myelin sheath, laying the foundation for degeneration and advancing our understanding of the intricate mechanisms underlying HSPs.

neuroscience↗

A novel approach to quantifying inter-individual distance in insects

1Behaviour involving two or more individuals within the same species is known as social behaviour. Sexual dimorphisms and environmental cues as well as age, experience and social hierarchy shape social behaviour. The study of this complex behaviour, however, has one essential boundary condition: the distance between individuals. Because social signals (e.g. acoustic, visual or olfactory) have limited reach the inter-individual distance is crucial for the correct transmission of such signals. In this study we present a newly developed assay to study group behaviour and inter-individual distance in Drosophila melanogaster. This assay consists of a circular observation space flanked by two automatic release devices that allow flies to enter individually. By releasing the flies one at a time, the observer can study different features of (intra-)group behaviour with different group compositions. Importantly, the observer can control (manually or through automatisation) the increase of group size over time. Over the last decades insects became more relevant as convenient model organisms to study the neurophysiological and genetic basis of (human) neuro-developmental disorders. Drosophila models are used to study the genetic and neuronal underpinnings of a wide range of neurological disorders. In some cases the studies revealed alterations in social behaviour consistent with descriptions of behavioural symptoms in human disorders. Social behaviours in Drosophila are well-studied and include courtship, mating, aggression and group interactions. This setup will facilitate the analysis of these aspects of group interactions in Drosophila, allowing for a deeper understanding of the neuronal circuits and genetic factors involved in those behaviours. 2 Contribution to the fieldSocial behaviour pertains to the most sophisticated behavioural feats, as it involves multiple, interacting individuals. These complex interactions often conceal the underlying neuronal and ethological mechanisms. One of the most basal ethological mechanisms is the inter-individual distance, which resembles a perimeter in which each individual needs to formulate a response to the approach of others. We introduce a device that allows to test the inter-individual distance under consistent circumstances, by automating the entry time and direction of conspecifics into the arena. We can further observe the composition, dynamics and forming of larger animal groups as well as their separating. We can also observe how the individual distances alter during the process. Also other behaviours can be easily observed, e.g. aggression, courtship, homosexual courtship, etc. We successfully employed this approach in [1] and could discriminate the role of different neuroligins in social behaviour. We provide a detailed description including building plans and material lists for this social observation device. The system can be run in an automatic mode to ensure the consistency of experiments or in a manual mode to test animals under more flexible social situations. We provide multiple back lighting systems to test animals in the dark (infra-red LEDs) or in illuminated environments (vis. range LEDs). The system is fully automated and can be linked with a number of animal trackers (e.g. T-Rex, deeplabcut, LACE, etc.) via simple videography. We hope that our experimental setup augments the variety of behaviours testable in ethological setups (T-maze, water-mazes, operant conditing setups, etc) with social interaction and group formation.

animal behavior and cognition↗

Cold trapped - Correcting locomotion dependent observation biases in thermal preference of Drosophila

Sensing environmental temperatures is essential for the survival of ectothermic organisms. In Drosophila, two methodologies are used to study temperature preferences (TP) and the genes involved in thermosensation: two-choice assays and temperature gradients. Whereas two-choice assays reveal a relative TP, temperature gradients can identify the absolute Tp. One drawback of gradients is that small ectothermic animals are susceptible to cold-trapping: a physiological inability to move at the cold area of the gradient. Often cold-trapping cannot be avoided, biasing the resulting TP to lower temperatures. Two mathematical models were previously developed to correct for cold-trapping. These models, however, focus on group behaviour which can lead to overestimation of cold-trapping due to group aggregation. Here we present a mathematical model that estimates the behaviour of individual Drosophilain temperature gradients. The model takes the spatial dimension and temperature difference of the gradient into account, as well as the rearing temperature of the flies. Furthermore, it allows quantifying cold-trapping, reveals true TP, and differentiates between temperature preference and tolerance. Online simulation is hosted at http://igloo.uni-goettingen.de. The code can be accessed at https://github.com/zerotonin/igloo.

neuroscience↗