Name: Open Field Test in an Angelman Syndrome Mouse Model
Uploaded: 2023-10-20T12:10:00
Description: Watch this Scientific Journal Video about Open Field Test in an Angelman Syndrome Mouse Model at JoVE.com

open field test in an angelman syndrome mouse model

Validación de un modelo murino del síndrome de Angelman mediante pruebas conductuales

Angelman syndrome (AS) is a rare neurodevelopmental disease. The most common genetic origin of AS is a large deletion of the 15q11-q13 region of the maternally-derived chromosome, which is found in nearly 74% of patients1. Deletion of this region causes the loss of UBE3A, the main causative gene of AS that encodes an E3 ubiquitin ligase. The paternal allele of the UBE3A gene in neurons is silenced in a process known as imprinting. As a consequence, paternal imprinting of the gene allows only maternal expression in the central nervous system (CNS)2. Therefore, UBE3A gene deletion from the maternally-derived chromosome leads to the development of AS symptoms. In humans, AS manifests at around 6 months of age, with developmental retardation that persists throughout all developmental stages and results in severe debilitating symptoms in affected individuals3,4. The core symptoms of the disorder include the deficit of fine and gross motor skills, including jerky ataxic gait, serious speech impairment, and intellectual disability. Approximately 80% of AS patients also suffer from sleep disturbances and epilepsy. To date, the only available treatment are symptomatic drugs, which reduce epileptic seizures and improve sleep quality1. Therefore, the development of robust animal models with reproducible behavioral phenotypes alongside refined phenotyping analysis will be essential to elucidate the pathophysiological mechanisms of the disorder and discover effective medications and treatments.
The complexity of the human disorder affecting the CNS demands model organisms to possess a comparable genome, physiology, and behavior. Mice are popular as a model organism due to their short reproductive cycle, small size, and relative ease of DNA modification. In 1984, Paul Willner proposed three basic disease model validation criteria: the construct, face, and predictive validity, which are used to determine the model&#39;s value5. Simply, construct validity reflects the biological mechanisms responsible for the disorder development, face validity recapitulates its symptoms, and predictive validity describes the model response to therapeutic drugs.
To adhere to the above principles, we have chosen the most common genetic etiology, a large deletion of the maternal 15q11.2-13q locus including the UBE3A gene, to create AS model mice. We used the CRISPR/Cas9 technique to delete a 76,225 bp long region spanning the entire UBE3A gene, encompassing both the coding and non-coding elements of the gene, in mice from a C57BL/6N background6. We then bred the animals to obtain UBE3A+/&#8722; heterozygous mice. For face validation of the model, we used animals from crosses of UBE3A+/&#8722; females and wild-type males to gain UBE3A+/- progeny (strain named C57BL/6NCrl-UBE3A&#60;em1(IMPC)Ccpcz&#62;/Ph and later assigned as UBE3AmGenedel/+) and control littermates. We tested their fine and gross motor skills, emotionality, and affect to recapitulate core AS symptoms. In a previous article, we also evaluated the animals&#39; cognitive functions, as AS patients also suffer from intellectual disability6. However, we found no cognitive impairments in UBE3AmGenedel/+ mice, perhaps due to the young age of the animals at the time of testing7. Later examination of the older animals, around 18 weeks old, revealed a deficit in behavioral flexibility during reversal learning in the place preference paradigm. However, the complexity of the employed equipment for this analysis requires a separate methodological module and it is not included here.
The behavioral tests presented here belong to the common phenotyping tools in genetic research, thanks to their high predictive value and sufficient construct validity8,9,10. We used these tests to validate a mouse model of AS by recapitulating core symptoms of the human disease in a reproducible, age-independent manner. The emotionality of the animal was evaluated in the elevated plus maze and open field tests. Both of these tests are based on the approach-avoidance conflict, where animals explore a new environment in search of food, shelter, or mating opportunities while simultaneously avoiding anxiogenic compartments11. Additionally, the open field test is used to test a mouse&#39;s locomotor activity8. The tail suspension test is widely used in depression research to screen for new antidepressant drugs or depressive-like phenotypes in mouse knockout models12. This test evaluates the despair that animals develop over time in an inescapable situation. Motor learning and detailed gait characteristics were determined on the rotarod and in DigiGait, respectively. Animal endurance on the accelerating rod characterizes its balance and movement coordination skills, while detailed analysis of a mouse&#39;s step patterns is a sensitive evaluation of neuromuscular impairments connected to many neurogenerative movement disorders13,14,15. The nestlet shredding test is part of the standard methodology for detecting impulsive behavior in rodents, and since it utilizes natural rodent building behavior, it indicates the animal&#39;s well-being16,17.
The size of the experimental groups was a result of a compromise to meet the 3R rule demands and efficient usage of colony breeding performance. However, to obtain statistical power, the groups had no fewer than 10 individuals, due to the establishment of a sufficient amount of breeding pairs. Unfortunately, breeding performance did not always result in a sufficient number of animals.

Author Spotlight: Una batería de pruebas conductuales altamente reproducibles para validar un modelo murino de síndrome de Angelman 

Caracterización conductual de un modelo de ratón con síndrome de Angelman

Our goal is to elucidate the physiological roles of genes using mice as an experimental model. We also focus on developing mouse models of specific diseases that scientists can use to investigate disease causation and develop effective treatments. An example of such activity is the mouse model of Angelman syndrome.Arguably, the most promising new technology with potential is integrating artificial intelligence based on deep learning techniques in animal research. This approach can be used to monitor animal behavior in the home cage directly without need for the experimenter to disturb the animals. The biggest challenge in behavioral studies currently is reproducibility.Therefore, we introduce a battery of tests that validate the Angelman syndrome of model in a way that does not depend on the model's age or species. We use established behavioral tests to validate our AS model. However, with the novel approach for the model development closely resembling the human condition with a large deletion.Using CRISPR technology, we deleted the entire UBE3A gene from the mouse genome. In contrast to other models where the deletion is limited to 3KB. We're working on developing a genetic therapy that could restore a symptoms in a mouse model.

Watch this Scientific Journal Video about Open Field Test in an Angelman Syndrome Mouse Model at JoVE.com

Open Field Test in an Angelman Syndrome Mouse Model  

Prueba de campo abierto en un modelo de ratón con síndrome de Angelman

Coloque las cuatro cajas de prueba de campo abierto, o OF, en la plataforma de prueba debajo de la cámara. Usando el potenciómetro en la pared, ajuste la intensidad de la luz a 200 lux en el centro de cada prueba OF con la ayuda de un luxómetro con su sensor colocado en el centro de cada caja durante el ajuste. Abra el software haciendo doble clic en el icono del software del visor y cargue la configuración para las pruebas de EF haciendo clic en el icono de la parte superior izquierda de la pestaña de configuración.Introduzca la información del animal en los campos correspondientes de la pestaña del experimento. Verifique que la posición de la zona coincida con las casillas de prueba OF y ajústelas si es necesario. Con un control visual y un mouse de computadora, asegúrese de que el centro de contorno virtual y las zonas periféricas coincidan con las zonas de prueba OF correspondientes.Coloque el cursor del ratón sobre el icono de flecha en la parte superior izquierda de la pestaña de adquisición. Saca cuatro animales de la jaula de la casa y colócalos en la esquina de cada caja de prueba. Detenga el experimento haciendo clic con el botón izquierdo en el mouse de la computadora.En la prueba de FO, los animales mutantes heterocigotos maternos Ube3a fueron significativamente hipoactivos, como se refleja en una distancia recorrida más corta, una velocidad media más baja y un tiempo de descanso más largo. Sin embargo, ninguno de los parámetros relacionados con el comportamiento similar a la ansiedad se alteró en los mutantes Ube3a.

Research

JoVE Journal

Behavior

Open Field Test in an Angelman Syndrome Mouse Model

Behavioral Characterization of an Angelman Syndrome Mouse Model

This manuscript describes a battery of behavioral tests available to characterize Angelman syndrome (AS)-like phenotypes in an established murine model of ...

Investigación

Comportamiento

Elevated Plus Maze Test in an Angelman Syndrome Mouse Model

Prueba de laberinto elevado plus en un modelo de ratón con síndrome de Angelman

Tail Suspension Test in an Angelman Syndrome Mouse Model

Prueba de suspensión de cola en un modelo de ratón con síndrome de Angelman

Gait Analysis in an Angelman Syndrome Mouse Model

Análisis de la marcha en un modelo de ratón con síndrome de Angelman

Rotarod Test in an Angelman Syndrome Mouse Model

Prueba de Rotarod en un modelo de ratón con síndrome de Angelman

Nestlet Shredding: Nest Building Test in an Angelman Syndrome Mouse Model

Nestlet Shredding: Prueba de construcción de nidos en un modelo de ratón con síndrome de Angelman