Dendritic cells are specialized antigen-presenting cells that regulate immunity and tolerance. Chemokine receptor 7 (CCR7), which is expressed by mature dendritic cells, mediates the migration of the cells to secondary lymphoid organs and thus regulates immune responses. It has been demonstrated that immature dendritic cells can induce immune tolerance, but they do not express CCR7 and cannot migrate to secondary lymphoid organs. We transfected immature dendritic cells with a recombinant adenovirus carrying the CCR7 gene to obtain immature dendritic cells with the ability to migrate. The maturity of the cells was monitored by scanning electron microscopy and flow cytometry. In addition, we assessed the ability of cells to migrate and the function of the cells using in vitro chemotactic and mixed leukocyte reaction assays. The results showed that immature dendritic cells became semi-mature, exhibiting a mild upregulation of co-stimulatory molecular expression and a few dendritic processes. Immunofluorescence assay and Western blotting indicated that CCR7 protein expression increased significantly in immature dendritic cells following CCR7 gene transfection. The in vitro chemotactic assay showed a significantly enhanced ability to migrate in response to CCL19 following CCR7 gene transfection. Moreover, transfected cells showed an enhanced ability to stimulate allogeneic T cell proliferation in vitro, but their ability was significantly weaker than that of mature dendritic cells. Interleukin-10 inhibited the differentiation and maturation of immature dendritic cells. It is concluded that, following CCR7 gene transfection, immature dendritic cells exhibit an enhanced ability to migrate and some of the characteristics of mature cells. Thus, these cells are of potential clinical significance in studies of immune tolerance induction during skin grafting after severe burns.
We report the application of three-dimensional positron emission tomography/computed tomography (PET/CT) for the analysis of (13)NO(3)(-) uptake and (13)N distribution in growing kohlrabi. The analytical procedures, equipment parameters, and image reconstruction mode for plant imaging were tested and selected. (13)N in growing kohlrabi plants was imaged versus time using both PET movies and PET/CT tomograms. The (13)NO(3)(-) transport velocity in kohlrabi from root to petiole was estimated to be 1.0 cm/min. The appearance of shell-shaped (13)NO(3)(-) transport pathways, corresponding to the kohlrabi corm, suggests the existence of special routes with higher efficiency for (13)NO(3)(-) transport, which tends to have the shortest distances to the leaves or buds. Standardized uptake values (SUVs), used as the representative figures for describing (13)N distribution, were quantified versus time at some putative sites of interest. For multiple analysis of the same-plant, (13)N distribution in kohlrabi under normal conditions, methionine sulfoximine (MSX) stress, and recovery from MSX stress was examined. The (13)N distribution variation studies were also done under the above three growth conditions. Our results suggest a significant downregulation of nitrate uptake in kohlrabi in the presence of MSX.
Malignant gliomas, the most common type of primary brain tumor, account for 80% of malignant tumors in the central nervous system (CNS). There are three principal types of glioma: astrocytomas, oligodendrogliomas, and oligoastrocytomas. Glioma stem cells (GSCs) have been found in all types; however, many fundamental questions about GSCs remain unanswered. This review will examine the current state of knowledge regarding GSC origin and the signaling pathways implicated in GSC tumorigenesis. The outstanding challenges for the study of GSCs in the context of glioma progression will also be discussed.
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