31 research outputs found

    The Recognition of Hypothalamo-Neurohypophysial Functions by Developing T Cells

    Get PDF
    Neuropeptide signals and specific neuropeptide receptors have been described in the thymus supporting the concept of a close dialogue between the neuroendocrine and the immune systems at the level of early T-cell differentiation. In this paper, we review recent data about neurohypophysial (NHP)-related peptides detected in the thymus from different species. We suggest that we are dealing in fact with other member(s) of the NHP hormone family, which seems to exert its activity locally through a novel model of cell-to-cell signaling, that of cryptocrine communication. This model involves exchange of signals between thymic epithelial cells and developing thymocytes. The NHP-related peptides have been shown to trigger thymocyte proliferation and could induce immune tolerance of this highly conserved neuroendocrine family

    Distribution of phosphatase activity and various bacterial phyla in the rhizosphere of <em>Hordeum vulgare</em> L. depending on P availability.

    No full text
    Despite the importance of the rhizosphere for nutrient turnover, little is known about the spatial patterns of organic phosphorus mineralization by plants and by microorganisms in the rhizosphere. Therefore, the distribution of acid and alkaline phosphatase activity and the abundance of bacteria belonging to various bacterial phyla were investigated in the rhizosphere of barley (Hordeum vulgare L.) as dependent on the availability of inorganic P. For this purpose, we conducted a greenhouse experiment with barley growing in inclined boxes that can be opened to the bottom side (rhizoboxes), and applied soil zymography and fluorescence-in situ-hybridization (FISH). Acid phosphatase activity was strongly associated with the root and was highest at the root tips. Due to P fertilization, acid phosphatase activity decreased in the bulk soil, and less strongly in the rhizosphere. Alkaline phosphatase activity, i.e., microbial phosphatase activity was high throughout the soil in the control treatment and was reduced due to inorganic P fertilization especially in the rhizosphere and less strongly in the bulk soil. P-fertilization slightly increased the total number of bacteria in the rhizosphere. Moreover, P-fertilization decreased the abundance of Firmicutes and increased the abundances of Beta- and Gamma-Proteobacteria. The total number of bacterial cells was significantly higher at the root surface than at the root tip and at a distance of 30&nbsp;&mu;m from the root surface. Our results show that alkaline phosphatase activity decreased more strongly in the rhizosphere than in the bulk soil due to P fertilization, which might be because of greater C deficiency in the bulk soil compared to the rhizosphere. Furthermore, the results indicate a spatial separation between hotspots of acid phosphatase activity and hotspots of bacteria in the rhizosphere of H.&nbsp;vulgare. Taken together, our study shows that bacteria and phosphatase activity were very heterogeneously distributed in soil, and that the effects of P fertilization on phosphatase activity differed strongly between bulk soil and rhizosphere as well as between various zones of the rhizosphere

    Influence of follicular dendritic cells on the survival of lymphocytes in vitro

    Full text link
    To study the role of follicular dendritic cells (FDC) in germinal centers, we tried to keep them alive in vitro by culturing entire lymphoid follicles. Ultrastructural studies of those cultures in different conditions of culture technique, medium and temperature have been made. In any considered conditions living FDC were not found in the cultures after the 7th day. But during that period, only lymphocytes in close contact with the cytoplasmic processes of FDC survived. FDC seem thus to exert a positive action on lymphocyte survival in vitro. Moreover, FDC and lymphocytes appeared associated in situ in clusters similar to those obtained after isolation of FDC (Lilet-Leclercq et al., J. Immunol. Meth., 1984, 59, 235)
    corecore