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dc.contributor.advisorPetroff, Margaret Gen_US
dc.contributor.authorWarren, Bryce
dc.date.accessioned2015-03-16T22:45:05Z
dc.date.available2015-03-16T22:45:05Z
dc.date.issued2014-12-31en_US
dc.date.submitted2014en_US
dc.identifier.otherhttp://dissertations.umi.com/ku:13669en_US
dc.identifier.urihttp://hdl.handle.net/1808/17098en_US
dc.description.abstractThe Autoimmune Regulator (AIRE) contributes to central immune tolerance through the induction of self-antigen expression within the thymus. In humans, a defect in AIRE results in a multi-organ autoimmune disorder known as Autoimmune Polyglandular Syndrome Type-1. Both humans and mice with a deficiency in this gene develop autoreactive CD4+ T cells, serum autoantibodies and elevated rates of infertility. Interestingly, the pathology of autoimmune infertility in Aire-deficient (Aire-KO) mice differs between males and females. Ovarian autoimmunity causing a depletion of follicular reserves is prominent in female Aire-KO mice over 10 weeks of age. However, 50% of mated six-week old female Aire-KO mice demonstrate embryo loss by embryonic day (ED) 7.5 despite having normal follicular reserves. We determined that ovulation (90% KO vs 100% WT; n=11), mating frequency (99% KO vs 100% WT; n>58), progesterone production (p=0.232; n=4) and decidualization are unaffected. However, 60% (9 of 15) of 6-8 week old Aire-KO female mice generated serum autoantibodies against the ovary and more frequently ovulated degenerated oocytes (31% KO vs 2% WT; n>71) When cultured, one-cell embryos from Aire-KO females failed to become 2-cell and blastocyst stage embryos at significantly reduced rate compared to WT controls (47% KO vs 76% WT and 19% KO vs 60% WT; n>67). Finally, embryos from Aire-KO dams are developmentally delayed at ED3.5 with a reduced trophectoderm outgrowth potential after 48 and 96 hours of culture (0mm2 KO vs 7.1 mm2 WT, and 16.5 mm2 KO vs 30.9 mm2 WT; p58), progesterone production (p=0.232; n=4) and decidualization are unaffected. However, 60% (9 of 15) of 6-8 week old Aire-KO female mice generated serum autoantibodies against the ovary and more frequently ovulated degenerated oocytes (31% KO vs 2% WT; n>71) When cultured, one-cell embryos from Aire-KO females failed to become 2-cell and blastocyst stage embryos at significantly reduced rate compared to WT controls (47% KO vs 76% WT and 19% KO vs 60% WT; n>67). Finally, embryos from Aire-KO dams are developmentally delayed at ED3.5 with a reduced trophectoderm outgrowth potential after 48 and 96 hours of culture (0mm2 KO vs 7.1 mm2 WT, and 16.5 mm2 KO vs 30.9 mm2 WT; p71) When cultured, one-cell embryos from Aire-KO females failed to become 2-cell and blastocyst stage embryos at significantly reduced rate compared to WT controls (47% KO vs 76% WT and 19% KO vs 60% WT; n>67). Finally, embryos from Aire-KO dams are developmentally delayed at ED3.5 with a reduced trophectoderm outgrowth potential after 48 and 96 hours of culture (0mm2 KO vs 7.1 mm2 WT, and 16.5 mm2 KO vs 30.9 mm2 WT; p67). Finally, embryos from Aire-KO dams are developmentally delayed at ED3.5 with a reduced trophectoderm outgrowth potential after 48 and 96 hours of culture (0mm2 KO vs 7.1 mm2 WT, and 16.5 mm2 KO vs 30.9 mm2 WT; p83 oocytes). Additionally a subset of males (23%; n=22) exhibited oligozoospermia with disruption of the blood-testis barrier. Collectively these results demonstrate the importance of central immune tolerance on fertility preservation by preventing autoimmune disease against the male and female reproductive systems.
dc.format.extent195 pagesen_US
dc.language.isoen_USen_US
dc.publisherUniversity of Kansasen_US
dc.rightsThis item is protected by copyright and unless otherwise specified the copyright of this thesis/dissertation is held by the author.en_US
dc.subjectBiology
dc.subjectImmunology
dc.subjectCellular biology
dc.subjectAIRE
dc.subjectAutoimmune regulator
dc.subjectinfertility
dc.subjectoligozoospermia
dc.subjectorchiepididymitis
dc.subjectprimary ovarian insufficiency
dc.titleThe Autoimmune Regulator (AIRE) preserves fertility in male and female Balb/c mice.
dc.typeDissertationen_US
dc.contributor.cmtememberAbrahamson, Dale R
dc.contributor.cmtememberChristenson, Lane K
dc.contributor.cmtememberWright, Douglas E
dc.contributor.cmtememberYankee, Thomas M
dc.thesis.degreeDisciplineAnatomy & Cell Biology
dc.thesis.degreeLevelPh.D.
dc.rights.accessrightsopenAccessen_US


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