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dc.contributor.advisorCiolino, Henry P.en
dc.contributor.advisorJolly, Christopher A.en
dc.creatorGulvady, Apeksha Ashoken
dc.date.accessioned2012-11-29T22:08:30Zen
dc.date.available2012-11-29T22:08:30Zen
dc.date.created2011-05en
dc.date.issued2012-11-29en
dc.date.submittedMay 2011en
dc.identifier.urihttp://hdl.handle.net/2152/ETD-UT-2011-05-3276en
dc.descriptiontexten
dc.description.abstractApproximately two-thirds of US adults are overweight or obese, and obesity is also becoming more prevalent in children and adolescents. Similar to adults, obese children are at a higher risk of developing health problems due in part to dysfunctional immune surveillance. Obesity has been shown reduce the generation of new T-cells by accelerating thymic aging in an adult mouse. This study therefore aimed at determining whether similar diet induced obesity (DIO) changes can be induced in a young mouse. Comparisons made between lean and DIO C57Bl/6 mice showed a significant increase in thymic weight, decrease in thymic cellularity and thymic output, and impaired T-cell development at the double negative stage. We associate these alterations with changes in thymic architecture and accumulation of lipid droplets within the thymic cortex and medulla of the obese mice. The above observations indicate that DIO can induce fat accumulation and reduce thymic function at a young age. Resveratrol, a natural polyphenolic compound, was then used to regulate fat metabolism in an attempt to reduce these DIO changes we observed. Resveratrol induces fat oxidation via 5' adenosine monophosphate-activated protein kinase (AMPK), and its reciprocal regulation of glycerol-3-phosphate acyltransferase-1 (GPAT-1) and carnitine palmitoyltransferase-1 (CPT-1), the rate-limiting enzymes required for glycerophospholipid biosynthesis and oxidation, respectively. Through resveratrol feeding, we were able to prevent the effects of DIO on thymic architecture and thymic T-cell proliferation. This was achieved by manipulating AMPK into inhibiting GPAT-1 and enhancing CPT-1 activity. Since the expression of GPAT-1 was upregulated in the obese mice, we investigated whether deleting GPAT-1 altogether might prevent the thymic involution, by inhibiting synthesis of glycerophospholipids and triacylglycerol. Instead, we found that GPAT-1 deletion slowed thymic growth and reduced cellularity in young mice, which we associated with impaired thymic T-cell function and development, suggesting that the deleterious effects of GPAT-1 deficiency may be due to perturbations in thymic T-cell activation and signaling. These data provide a novel link between lipid metabolism and T-cell development, and identify the use of the naturally-occurring resveratrol to reduce lipid accumulation within the involution-prone thymus, thus providing a useful approach to preventing a decline in thymic function in childhood.en
dc.format.mimetypeapplication/pdfen
dc.language.isoengen
dc.subjectThymusen
dc.subjectObesityen
dc.subjectT-cellen
dc.subjectResveratrolen
dc.subjectAMPKen
dc.subjectGPAT-1en
dc.subjectCPT-1en
dc.titleThe influence of obesity and lipid metabolism on thymic functionen
dc.date.updated2012-11-29T22:08:40Zen
dc.identifier.slug2152/ETD-UT-2011-05-3276en
dc.contributor.committeeMemberSanders, Bob G.en
dc.contributor.committeeMemberKline, Kimberlyen
dc.contributor.committeeMemberRichie, Ellen R.en
dc.contributor.committeeMemberMaynard, Jennifer A.en
dc.description.departmentNutritional Sciencesen
dc.type.genrethesisen
thesis.degree.departmentNutritional Sciencesen
thesis.degree.disciplineNutritional Sciencesen
thesis.degree.grantorUniversity of Texas at Austinen
thesis.degree.levelDoctoralen
thesis.degree.nameDoctor of Philosophyen


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