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dc.contributor.advisor Jameson, Julie en_US
dc.contributor.author Park, Christa
dc.date.accessioned 2017-08-11T18:03:04Z
dc.date.issued 2017-08-11
dc.date.submitted 2017-08-10
dc.identifier.uri http://hdl.handle.net/10211.3/194723
dc.description.abstract According to the Journal of the American Medical Association and the Centers for Disease Control and Prevention, one in six children and adolescents in the United States are obese. Obesity is a metabolic disease caused by a caloric imbalance, which leads to an accumulation of excess fat in the body. Adipose tissue constitutes an endocrine organ that can become unregulated as it expands and cause chronic systemic inflammation. There is a strong correlation between obesity and inflammatory conditions such as inflammatory bowel disease. In addition, the gastrointestinal problems encountered in obese youth are more severe than in patients whose obesity manifests in adulthood. Although intraepithelial lymphocytes are known to improve intestinal barrier function and decrease the severity of inflammatory bowel disease, it is unknown whether intraepithelial lymphocytes are impacted by obesity. An established murine model of obesity was used to examine the relationship between the developmental stage of obesity onset and the ability of intraepithelial lymphocytes to seed in the intestine, maintain normal numbers and function in barrier protection. Since intraepithelial lymphocytes seed in the intestine early in childhood and proliferate locally to produce numbers that are maintained throughout adulthood, we hypothesized that these immune cells may be especially sensitive to obesity at an early age. Immunohistochemistry and flow cytometry were used to examine intraepithelial T cell number and function in the intestine of mice that experienced controlled onsets of obesity at stages similar to child, adolescence, and adulthood of humans. Intraepithelial lymphocytes were significantly reduced in all three stages of maturation after consuming a high fat diet. Obese weanling mice exhibited the fewest intraepithelial lymphocytes as compared to the obese adolescent and obese adult mice. However, T cell subsets in adolescent and adult mice were more severely skewed toward inflammatory populations with elevated TNF-a production than T cell subsets in weanling mice. Both factors may result in problems with barrier function and contribute to the increased severity of inflammatory bowel disease. Together these results demonstrate that the age at which weight gain is initiated is important in the pathogenesis of intestinal disease in obesity. en_US
dc.description.sponsorship Biological Science en_US
dc.language.iso en_US en_US
dc.subject T cell en_US
dc.subject Mice en_US
dc.subject Obesity en_US
dc.title The Impact of Obesity on Intestinal Epithelial T Cell Number and Function in Mice in Different Stages of Maturity en_US
dc.type Thesis en_US
dc.description.embargoterms 3 years en_US
dc.date.embargountil 2020-08-10T18:03:04Z
dc.contributor.committeemember Kristan, Deborah en_US
dc.contributor.committeemember D'anna Hernandez, Kimberly en_US


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