Donna M. Fluitsma

Mannose Receptor Mediated Antigen Uptake and Presentation in Human Dendritic Cells

In an immature state, dendritic cells (DC) can capture antigen via at least two mechanisms. First, DC use macropinocytosis for continuous uptake of large amounts of soluble antigens. Second, they express high levels of mannose receptor that can mediate internalization of glycosylated ligands. We found that dendritic cells can present mannosylated antigen 100-1000 fold more efficiently than non-mannosylated antigen. Immunocytochemistry as well as subcellular fractionation demonstrated that the mannose receptor and MHC class II molecules were located in distinct subcellular compartments. These results demonstrate that the mannose receptor endows DC with a high capacity to present glycosylated antigens at very low concentrations.

Dithiocarbamates are teratogenic to developing zebrafish through inhibition of lysyl oxidase activity

Dithiocarbamates (DTCs) are a class of compounds that are extensively used in agriculture as pesticides. As such, humans and wildlife are undoubtedly exposed to these chemicals. Although DTCs are thought to be relatively safe due to their short half lives, it is well established that they are teratogenic to vertebrates, especially to fish. In zebrafish, these teratogenic effects are characterized by distorted notochord development and shortened anterior to posterior axis. DTCs are known copper (Cu) chelators but this does not fully explain the observed teratogenic effects. We show here that DTCs cause malformations in zebrafish that highly resemble teratogenic effects observed by direct inhibition of a group of cuproenzymes termed lysyl oxidases (LOX). Additionally, we demonstrate that partial knockdown of three LOX genes, lox, loxl1 and loxl5b, sensitizes the developing embryo to DTC exposure. Finally, we show that DTCs directly inhibit zebrafish LOX activity in an ex vivo amine oxidase assay. Taken together, these results provide the first evidence that DTC induced teratogenic effects are, at least in part, caused by direct inhibition of LOX activity.

Development of Exudate-Resident Macrophages, on the Basis of the Pattern of Peroxidatic Activity in Vivo and in Vitro

The diaminobenzidine (DAB) technique developed by Graham and Karnovsky (1966) has been widely used in the study of the localization of peroxidatic activity in various types of cell, including macrophages. On the basis of the intercellular distribution of peroxidatic activity, two types of macrophage have been distinguished, viz. resident macrophages and exudate macrophages. There are discrepancies between the findings of different authors as well as differences between the animal species used, as described below.