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dc.contributor.advisor Zhuang, Yuan en_US
dc.contributor.author Mahlios, Joshua en_US
dc.date.accessioned 2012-09-04T13:17:37Z
dc.date.issued 2012 en_US
dc.identifier.uri http://hdl.handle.net/10161/5867
dc.description Dissertation en_US
dc.description.abstract <p>Proper regulation of the immune system with regards to development, reaction specificity, and duration is necessary to prevent immune reactions directed against the host that can have a number of potentially lethal consequences. This regulation is controlled in part through a wide variety of transcription factors that function to ensure the proper development, function, and regulation of the immune system. </p><p>E-proteins are widely expressed and have a multitude of functions in the immune system including proper lymphocyte development and function. E-proteins can be regulated by class V HLH factors, including the inhibitor of differentiation (Id). genes 1-4. Id proteins are expressed throughout the hematopoietic system and have crucial roles in cell fate decisions, differentiation and proliferation in a multitude of tissues and cell types.</p><p>Id3 plays a variety of important roles in the immune system including T cell homeostasis, activation, and effector function. The importance of Id3 has been demonstrated using a number of mouse models, and mice that lack Id3 develop an autoimmune condition similar to that of Primary Sjögren's syndrome (PSS). The goal of this dissertation is to further characterize disease initiation and progression in Id3-/- mice, with a focus on the specific targeting of exocrine glands and associated lymphoid tissues by the immune system. </p><p>T cells play a crucial role in the development of disease symptoms in Id3-/- mice, though much remains unknown about the relative contribution of the two major subsets of T cells, &#945;&#946; and &#947;&#948; T cells to disease severity. The importance of both &#945;&#946; and &#947;&#948; T cells is demonstrated in part by the use of two newly generated models, Id3/&#946;-/- and Id3/&#948;-/- mice, which lack &#945;&#946; or &#947;&#948; T cells, respectively. These mice have allowed for a better understanding of the relative contribution of T cells in disease initiation and progression in Id3-/- mice.</p><p>Analysis of serum cytokine levels show that Id3-/- mice develop elevated levels of IL-13 at an early age, and this cytokine is associated with impaired saliva function. Significant populations of IL-13+ T cells have been identified in the peri-glandular lymph nodes of Id3-/- mice, though it appears that there are significant IL-13 producing cells not of the T cell lineage. Reduction of serum IL-13 levels via anti-IL-13 antibody treatment resulted in improved saliva production in response to cholinergic stimulation and reduced the number of mast cells detected in the mandibular and lachrymal glands. The importance of IL-13 in the initiation and progression of exocrinopathy in Id3-/- is being further investigated using a recently acquired IL-13 reporter mouse model. Additionally, IL-13R&#945;1+ cells have been identified in and around the gland tissues of Id3-/- mice, and while the origin and function of these cells remains unknown, these cells have a potential to serve as a biomarker for disease progression and severity.</p><p>Lastly, analysis of Id3-/- mice reveals an increased presence of mast cells in the peri-glandular lymph nodes and gland tissues as compared to wild type controls. These mast cells are localized in areas of significant tissue remodeling, serve as a potential source of IL-13 and are associated with impaired saliva production. These findings suggest an important role of mast cells in disease development in Id3-/- mice. Together, these studies have revealed a number of findings that will likely contribute to our understanding of the initiation and progression of exocrinopathy in Id3-/- mice.</p> en_US
dc.subject Immunology en_US
dc.title Investigation of the initiation and progression of exocrinopathy in Id3-/- mice en_US
dc.type Dissertation en_US
dc.department Immunology en_US
duke.embargo.months 24 en_US
duke.embargo.release 2014-08-25

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