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There is now a CONTENT FREEZE for Mercury while we switch to a new platform. It began on Friday, March 10 at 6pm and will end on Wednesday, March 15 at noon. No new content can be created during this time, but all material in the system as of the beginning of the freeze will be migrated to the new platform, including users and groups. Functionally the new site is identical to the old one. webteam@gatech.edu
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Advisor:
J. Brandon Dixon, PhD (Georgia Institute of Technology)
Committee:
Susan Thomas, PhD (Georgia Institute of Technology)
Krishnendu Roy, PhD (Georgia Institute of Technology)
Rudolph Gleason, PhD (Georgia Institute of Technology)
Mark Nicolls, MD (Stanford University School of Medicine)
Investigation of functional lymphatic changes and the immune response during lymphedema development
The lymphatic system serves important roles in fluid balance and immune system regulation within the body. Through both passive and active transport of fluid, the lymphatic network transports interstitial fluid back into the circulatory system. When the lymphatic system fails, that excess fluid can no longer be properly transported back into the circulation. This leads to a disease called lymphedema, which manifests as swelling of distal limbs and normally occurs following injury to the lymphatic network. The mechanisms of lymphedema development are not completely understood, but the immune response is known to play an important role in lymphedema pathogenesis. The main goal of this thesis is to investigate both the functional response of the intact lymphatic vasculature and changes in leukocyte populations within draining lymph nodes (dLNs) during lymphedema progression. In the first aim, we used near-infrared (NIR) imaging techniques to quantify changes in lymphatic function in vivo following induction of lymphedema in mice using a novel lymphedema model. We specifically investigated the effect of two potential therapeutic mechanisms, antagonism of leukotriene B4 (LTB4) production and deletion of epsin, on lymphatic function following lymphedema surgery. Further in vivo and ex vivo analysis was performed to elucidate potential mechanisms regulating the effect of LTB4 on lymphatic contractile function. In the second aim, we used flow cytometry to investigate changes in leukocyte populations within dLNs during acute lymphedema progression. Our novel lymphedema model leaves a pair of intact collecting lymphatic vessels on one side of the mouse tail while other tail lymphatics are ligated, allowing for analysis of the immune response within dLNs experiencing differences in drainage. Further analysis using a nanoparticle delivery system was used to quantify differences in particle uptake between dLNs as lymphedema progressed. The effect of LTB4 antagonism on the immune response was also elucidated. Overall, this work furthers understanding of the mechanisms driving lymphedema pathogenesis, by combining comprehensive analysis of changes in lymphatic contractile function in vivo and ex vivo with investigation of changes in the immune response within dLNs.
