Libri Novi

Ohne Zusammenfassung     

The morphology of the cement gland apparatus of Larval Pterophyllum scalare Cuv. & Val. (Cichlidae,Teleostei)

Summary The cement gland apparatus of newly hatched Pterophyllum scalare Cuv. & Val. was examined by histology, scanning and transmission electron microscopy. The whole organ is composed of three pairs of endoepithelial, ductless glands, which cause prominent elevations on the larval head and are found in a specific arrangement. Each single gland is represented by an aggregation of elongated, tubular secretory cells surrounding a pyriform acinus. It overlies a basal lamina and is covered by the outer layer of the bilaminar embryonic epidermis.Two different types of secretory cells can be distinguished. One type is restricted to the bottom of the cavity. It is characterized by multiform cytoplasmic protrusions, which project into the gland's cavity. The secretory granules contain a network of light filamentous material. The second type constitutes the side wall of the acinus. It does not develop any protrusions. The contents of the secretory granules is of very high and homogeneous electron density. The mechanism of extrusion is discussed for both cell types. All secretory cells show a strong PAS-reaction. In SEM a circular microridge pattern with attached mucus globules can be recognized on the larval epithelial surface.Dedicated to Prof. Dr. H. Leonhardt on the occasion of his 60th birthday     

HER-2/neu-mediated down-regulation of biglycan associated with altered growth properties

The extracellular matrix protein biglycan (Bgn) is a leucine-rich proteoglycan that is involved in the matrix assembly, cellular migration and adhesion, cell growth, and apoptosis. Although a distinct expression of Bgn was found in a number of human tumors, the role of this protein in the initiation and/or maintenance of neoplastic transformation has not been studied in detail. Using an in vitro model of oncogenic transformation, a down-regulation of Bgn expression as well as an altered secretion of different Bgn isoforms was found both in murine and human HER-2/neu oncogene-transformed cells when compared with HER-2/neu(-) cells. This was associated with a reduced growth, wound closure, and migration capacity. Vice versa, silencing of Bgn in HER-2/neu(-) fibroblasts increased the growth rate and migration capacity of these cells. Bgn expression was neither modulated in HER-2/neu(+) cells by transforming growth factor-β(1) nor by inhibition of the phosphoinositol 3-kinase and MAP kinase pathways. In contrast, inhibition of the protein kinase C (PKC) pathway led to the reconstitution of Bgn expression. In particular, the PKC target protein cAMP response element binding protein (CREB) is a major regulator of Bgn expression as the silencing of CREB by RNA interference was accompanied by ～5000-fold increase in Bgn-mRNA expression in HER-2/neu(+) cells. Thus, Bgn inhibits the major properties of HER-2/neu-transformed cells, which is inversely modulated by the PKC signaling cascade.     

Research progress on gut health of farmers teleost fish: a viewpoint concerning the intestinal mucosal barrier and the impact of its damage

Reviews in Fish Biology and Fisheries - The intestinal mucosal barrier plays a critical role in the maintenance of host health. In farmed teleost fish, the intestinal epithelium is challenged by a...     

Finding Evidence for Local Transmission of Contagious Disease in Molecular Epidemiological Datasets

Surveillance systems of contagious diseases record information on cases to monitor incidence of disease and to evaluate effectiveness of interventions. These systems focus on a well-defined population; a key question is whether observed cases are infected through local transmission within the population or whether cases are the result of importation of infection into the population. Local spread of infection calls for different intervention measures than importation of infection. Besides standardized information on time of symptom onset and location of cases, pathogen genotyping or sequencing offers essential information to address this question. Here we introduce a method that takes full advantage of both the genetic and epidemiological data to distinguish local transmission from importation of infection, by comparing inter-case distances in temporal, spatial and genetic data. Cases that are part of a local transmission chain will have shorter distances between their geographical locations, shorter durations between their times of symptom onset and shorter genetic distances between their pathogen sequences as compared to cases that are due to importation. In contrast to generic clustering algorithms, the proposed method explicitly accounts for the fact that during local transmission of a contagious disease the cases are caused by other cases. No pathogen-specific assumptions are needed due to the use of ordinal distances, which allow for direct comparison between the disparate data types. Using simulations, we test the performance of the method in identifying local transmission of disease in large datasets, and assess how sensitivity and specificity change with varying size of local transmission chains and varying overall disease incidence.