Browsing by Author "Greene, Catherine J"
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- ItemOpen AccessA role for cathepsin Z in neuroinflammation provides mechanistic support for an epigenetic risk factor in multiple sclerosis(2017-05-10) Allan, Euan R O; Campden, Rhiannon I; Ewanchuk, Benjamin W; Tailor, Pankaj; Balce, Dale R; McKenna, Neil T; Greene, Catherine J; Warren, Amy L; Reinheckel, Thomas; Yates, Robin MAbstract Background Hypomethylation of the cathepsin Z locus has been proposed as an epigenetic risk factor for multiple sclerosis (MS). Cathepsin Z is a unique lysosomal cysteine cathepsin expressed primarily by antigen presenting cells. While cathepsin Z expression has been associated with neuroinflammatory disorders, a role for cathepsin Z in mediating neuroinflammation has not been previously established. Methods Experimental autoimmune encephalomyelitis (EAE) was induced in both wildtype mice and mice deficient in cathepsin Z. The effects of cathepsin Z-deficiency on the processing and presentation of the autoantigen myelin oligodendrocyte glycoprotein, and on the production of IL-1β and IL-18 were determined in vitro from cells derived from wildtype and cathepsin Z-deficient mice. The effects of cathepsin Z-deficiency on CD4+ T cell activation, migration, and infiltration to the CNS were determined in vivo. Statistical analyses of parametric data were performed by one-way ANOVA followed by Tukey post-hoc tests, or by an unpaired Student’s t test. EAE clinical scoring was analyzed using the Mann–Whitney U test. Results We showed that mice deficient in cathepsin Z have reduced neuroinflammation and dramatically lowered circulating levels of IL-1β during EAE. Deficiency in cathepsin Z did not impact either the processing or the presentation of MOG, or MOG- specific CD4+ T cell activation and trafficking. Consistently, we found that cathepsin Z-deficiency reduced the efficiency of antigen presenting cells to secrete IL-1β, which in turn reduced the ability of mice to generate Th17 responses—critical steps in the pathogenesis of EAE and MS. Conclusion Together, these data support a novel role for cathepsin Z in the propagation of IL-1β-driven neuroinflammation.
- ItemOpen AccessExploring a Novel Late Stage Phagolysosomal Event in Macrophages(2020-09-17) Greene, Catherine J; Yates, Robin M.; Jirik, Frank; Biernaskie, JeffThe work presented in this thesis characterizes a novel late-stage phagolysosomal event of macrophages wherein the mature phagolysosome transiently fuses with the cellular membrane and releases its soluble but not particulate matter, a process we termed eructophagy. Phagosomal maturation through fusion and fission with the endolysosomal system was believed to be unidirectional, resulting in the degradation of phagocytosed cargo to basic building blocks. Through the development of a live-cell imaging assay to simultaneously monitor multiple phagolysosomal lumenal biochemistries in real-time, we observed eructophagy as an iterative process that occurred in certain phagolysosomes within a population of macrophages. Eructophagy was additionally observed in macrophages and dendritic cells from mice and humans. Upon further examination of eructophagy, we found that interferon-gamma (IFN-?) activation of macrophages significantly increased eructophagy but interleukin-4 (IL-4) activation almost completely inhibited eructophagy. Furthermore, macrophages derived from mice conditionally deficient in key autophagic proteins had impaired rates of eructophagy, suggesting a role for canonical autophagic machinery in eructophagy. Employing an shRNA screen of cellular fusion machinery associated with lysosomes, autophagosomes, and the cell membrane in macrophages derived from conditionally-immortalized myeloid precursor cells, we have constructed a potential fusion model of eructophagy. Pathogen and Damage-associated molecular patterns (PAMPS and DAMPS) are molecules from exogenous and endogenous sources respectively, that can induce innate immunity. Despite their recognition and downstream signaling being well established, little is known about how they are generated from larger source material. Here, we propose that eructophagy is a method of PAMP and DAMP dissemination through the release of partially-digested material from the phagolysosome. We demonstrate that phagolysosomal-dependent processing of CpG DNA and N-formyl peptides conjugated to particles within phagolysosomes occurs before their extracellular release, and subsequent activation of vicinal cells. Taken together, we present eructophagy as a novel phagolysosomal process of pro-inflammatory macrophages that is modulated by canonical autophagic machinery and utilizes fusion proteins associated with secretory autophagy. We propose that eructophagy offers a solution to the paradigm of how PAMPs and DAMPs are generated from larger source material before their dissemination.