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Identification of genes involved in macrophage activation and effector functions against intracellular pathogens
Includes bibliographical references.
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| Main Author: | |
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| Other Authors: | |
| Format: | Thesis |
| Language: | English |
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Division of Immunology
2014
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| _version_ | 1867613341611982848 |
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| access_status_str | Open Access |
| author | Schwegmann, Anita Ruth |
| author2 | Brombacher, Frank |
| author_browse | Brombacher, Frank Schwegmann, Anita Ruth |
| author_facet | Brombacher, Frank Schwegmann, Anita Ruth |
| author_sort | Schwegmann, Anita Ruth |
| collection | Thesis |
| description | Includes bibliographical references. |
| format | Thesis |
| id | oai:open.uct.ac.za:11427/9031 |
| institution | University of Cape Town (South Africa) |
| language | eng |
| last_indexed | 2026-06-10T12:34:36.552Z |
| license_str | Not specified — see source repository |
| provenance_str_mv | Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository |
| publishDate | 2014 |
| publishDateRange | 2014 |
| publishDateSort | 2014 |
| publisher | Division of Immunology |
| publisherStr | Division of Immunology |
| record_format | dspace |
| source_str | UCTD — University of Cape Town Open Access Repository |
| spelling | oai:open.uct.ac.za:11427/9031 Identification of genes involved in macrophage activation and effector functions against intracellular pathogens Schwegmann, Anita Ruth Brombacher, Frank Biochemistry Includes bibliographical references. This dissertation addressed the hypothesis that macrophages have an alternative killing mechanism that is independent of superoxide and nitric oxide but dependent on IFN-γ, TNF and C/EBPβ. Since the mechanism and the genes involved in this alternative pathway are mostly unknown, the aim of this dissertation was to identify these macrophage effector genes and to functionally characterize their role during infection utilizing gene deficient mouse models. Since mice deficient for C/EBPβ (C/EBPβ-/-) expressed normal levels of IFN-y and TNF during Listeria monocytogenes infection, the macrophage effector genes involved in confinement and killing of L. monocytogenes were postulated to be downstream of C/EBPβ. Furthermore, C/EBPβ-/- mice are highly susceptible L. monocytogenes due to impaired listericidal activity. Comparison of the gene expression profiles of WT and C/EBPβ-/- macrophages infected with L. monocytogenes was postulated to increase the probability of identifying these effector genes, which would be differentially expressed between the two groups. Comparative gene expression profiling by DNA microarrays between L. monocytogenes in infected WT and C/EBPβ-/- macrophages, successfully identified 1268 genes to be differentially expressed between the two groups. A focussed functional clustering strategy reduced the number of candidate genes to 220. PKCδ was selected for further study since it was involved in humoral defense, immune signalling, production of superoxide, regulation of transcription and may be putatively transcriptionally regulated by C/EBPβ. Furthermore, PKCδ was indirectly shown to promote L. monocytogenes escape from the phagosome and to negatively regulate transcription activity of C/EBPβ. In addition, since PKCδ was un-regulated, as shown by microarray and confirmed by RT-PCR, in L. monocytogenes infected C/EBPβ-/- macrophages, it was therefore thought to play a detrimental role during L. monocytogenes. However, since this premise has never been investigated directly, the role PKCδ during innate immunity against L monocytogenes was examined using the PKCδ deficient (PKCδ-/-) mouse model. Data in this dissertation provides new insight into the role of PKCδ during innate immunity to L. monocytogenes. PKCδ-/- mice were highly susceptible to L. monocytogenes due to enhanced listerial escape and impaired listericidal activity. Despite full macrophage activation and production of nitric oxide, PKCδ-/- mice displayed uncontrolled bacterial growth and dissemination of L. monocytogenes, which led to early death of the mice. In contrast, PKCδ-/- mice were able to control Mycobacterium infection as well as WT mice, suggesting that the activity of PKCδ may be negatively regulated by L. monocytogenes. A systems biology approach generated the hypothesis that PKCδ may promote Rab5a activation, which together with localized release of superoxide into the phagosome and activation of C/EBPβ by PKCδ, resulted in the confinement of the L. monocytogenes within the phagosome. Alternatively, PKCδ may act in a separate pathway that confines L monocytogenes within the phagosome, by activating and/or synergizing with unidentified proteins to neutralize that activity of listerial LLO and PI-PLC. Data in this dissertation clearly demonstrates that PKCδ is critical for confinement of L monocytogenes within phagosomes and may be part of a listericidal mechanism that is independent or nitric oxide, superoxide and pro-inflammatory cytokines. 2014-11-03T08:15:21Z 2014-11-03T08:15:21Z 2006 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/9031 eng application/pdf Division of Immunology Faculty of Health Sciences University of Cape Town |
| spellingShingle | Biochemistry Schwegmann, Anita Ruth Identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| thesis_degree_str | Doctoral |
| title | Identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| title_full | Identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| title_fullStr | Identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| title_full_unstemmed | Identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| title_short | Identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| title_sort | identification of genes involved in macrophage activation and effector functions against intracellular pathogens |
| topic | Biochemistry |
| url | http://hdl.handle.net/11427/9031 |
| work_keys_str_mv | AT schwegmannanitaruth identificationofgenesinvolvedinmacrophageactivationandeffectorfunctionsagainstintracellularpathogens |