Title page for ETD etd-11172005-185717

Type of Document Master's Thesis
Author Stalder, Mark Winston
Author's Email Address mstald1@lsu.edu
URN etd-11172005-185717
Title Neural Stem Cells as a Delivery Vector for Chemokine Expression in the Central Nervous System
Degree Master of Science (M.S.)
Department Pathobiological Sciences (Veterinary Medical Sciences)
Advisory Committee
Advisor Name Title
Karin E. Peterson Committee Chair
K. Gus Kousoulas Committee Member
Marlene S. Orandle Committee Member
  • spongiosis
  • retroviral recombination
  • in vivo gene expression system
  • spongiform degeneration
Date of Defense 2005-10-28
Availability unrestricted
Increased expression of cytokines and chemokines in the central nervous system (CNS) is closely associated with the development of retroviral-induced neurological diseases such as HIV-associated dementia, as well as other neuropathologies such as Alzheimer’s Disease and Multiple Sclerosis. The specific functions of many of these pro-inflammatory factors have yet to be elucidated in the disease process, and it is unclear whether the nature of their effects is protective, pathogenic, or both. Additionally, current models of chemokine function have inherent limitations, with direct injection resulting in a brief response that doesn’t accurately represent the effects of chronic production, and transgenic mice constitutively expressing chemokines by a large percentage of intrinsic brain cells from inception. This study takes the first step in developing a more representative in vivo system by which the direct of effects of the over-expression of individual CNS chemokines may be studied. C17.2 neural stem cells (NSC) were transduced with retroviral vectors containing the genes for CCL2, CCL7, CCL12, or the vector alone, and were inoculated into mice to generate a more accurate representation of the limited chemokine producing cell population that is seen with disease. The in vivo data generated herein suggests that this system is capable of consistently expressing comparable levels of these three chemokines, and characterizes the migration patterns of these cells into the major regions of the CNS. As no significant glial activation was seen concurrent with CCL over-expression, this study provides support for idea that the CCL chemokines may be involved in priming the CNS immune response, rather than its direct initiation. Additionally, ancillary histopathological data suggests a possible role for CCL12 in the development of spongiform lesions in the presence of recombinant retrovirus infection.
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