Filamentous fungi are multicellular eukaryotic organisms, which represent a separate taxonomic group organisms within the fungal kingdom, apart from the yeasts. These fungi always need a substrate... Show moreFilamentous fungi are multicellular eukaryotic organisms, which represent a separate taxonomic group organisms within the fungal kingdom, apart from the yeasts. These fungi always need a substrate to grow on, this can be living or dead material. Fungi possess the capacity to secrete high levels of enzymes. Because of this specific property, fungi are already used for centuries as miniature factories for the production of extracellular proteins. Aspergillus niger is an attractive organism because of its high secretion capacity and is frequently used as a model organism. Whereas high production yields can be obtained when homologous proteins are expressed, much lower amounts are obtained with the production of, heterologous proteins. This low protein yield is likely to be caused by impaired secretion of the heterologous protein. Evidence support the idea that a bottleneck for protein production is post-translational, possibly within the protein secretion pathway. To be able to improve heterologous protein secretion in fungi the (molecular) mechanism(s) of the protein secretion pathway was studied and resulted in this thesis. In Chapter 1 the knowledge about the secretory pathway in the yeast S. cerevisiae has been used as starting point to discuss and review different aspects of protein secretion in filamentous fungi. Special focus is on the comparison of the presence and function of secretion related small GTPases in yeasts, mammalian cells and filamentous fungi. Chapter 2 describes the visualisation of different cell organelles from A. niger using GFP-reporter proteins. To target GFP to a specific organelle, the GFP was fused to an organelle specific protein, or part of such a protein. In this way it was possible to visualize, nuclei, the endoplasmic reticulum (ER) and vacuoles. In addition, by fusing GFP to a protein that is efficiently secreted (glucoamylase), also the protein secretion process could be visualised. Chapter 3 describes the identification of several small GTPases in A. niger. The function of one of them, srgA, has been studied in more detail. In Chapter 4 the in depth functional characterisation of a second secretion related GTPase from A. niger named srgC is described. Here it is shown that this secretion related GTPase is specifically important for vacuolar biosynthesis which is visualized by the GFP-reporters described in chapter 2. In Chapter 5 a study on heterologous protein production in A. niger is described. Here a novel screening method is used based on a fusion protein between the well secreted A. niger glucoamylase protein fused with a laccase from Pleurotus ostreatus. With this method laccase hyper-secretion mutants were isolated. Show less
In rheumatoid arthritis, an inflammatory infiltrate accumulates and persists in the synovial membrane. Synovial T cells display a number of particular characteristics. While displaying markers of... Show moreIn rheumatoid arthritis, an inflammatory infiltrate accumulates and persists in the synovial membrane. Synovial T cells display a number of particular characteristics. While displaying markers of recent activation, synovial T lymphocytes respond poorly to mitogenic stimuli and their cytokine production appears to be suppressed both in situ and in vitro. One of the critical hallmarks from synovial T cells is that they suffer from oxidative stress. Oxidative stress in synovial fluid T lymphocytes inhibits T cell receptor (TCR)-dependent phosphorylation of pivotal signaling molecules, required for efficient T cell proliferation, and contributes to severe hyporesponsiveness of these cells. Chronic exposure of T lymphocytes to free radicals produced by activated phagocytic cells at the site of inflammation has been proposed to be the major cause of deregulated redox homeostasis in RA. In this thesis we further investigate the source of free radicals. We demonstrate that the oxidative stress found in synovial T cells is not the result from exogenous sources but originates from (an) intracellular activated oxidase(s). We demonstrate that the oxidase generating ROS in SF T cells is controlled by the small GTPases Ras and Rap1. We show that in synovial T cells Ras can be activated by a variety of cytokines. Rap1 inhibition is induced by direct cell-cell contact of T lymphocytes with antigen presenting cells (APC), and can be prevented by blocking the co-stimulatory T cell receptor CD28 with CTLA-4. Howevever, we did therapy with a nutrient supplement containing high dose anti-oxidants and poly-unsaturated fatty acids did not lead to clinical improvement of RA disease activity, nor therapy with high dose intravenously administered N-acetyl cysteine. Show less