Über Fibrillärstrukturen im Nebennierenmark von Haus und Wildmeerschweinchen (Cavia aperea f. porcellus L. und Cavia aperea tschudii Fitzinger)

Zusammenfassung Im Nebennierenmark von adulten Wildmeerschweinchen (Cavia aperea tschudii) und Hausmeerschweinchen (Cavia aperea f. porcellus) werden bisher unbekannte intrazelluläre Fibrillenstrukturen nachgewiesen. Licht- und elektronenmikroskopische Befunde zeigen, daß in bestimmten Markzellen Filamentbündel in Gruppen auftreten, die durch das Perikaryon bis zur Zellperipherie zu verfolgen sind. Sie fasern in der Nähe des Plasmalemms auf und bilden desmosomenähnliche Kontaktflächen. Die Einzelfilamente sind ca. 70–100 Å dick. Beim Chinchilla konnten im Mark keine Filamentstränge festgestellt werden, beim Haus- und Wildmeerschweinchen kommen sie in unterschiedlicher Häufigkeit vor.

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Intracellular fibrils in the adrenal medulla of domesticated and wild guinea pigs (Cavia aperea f. porcellus L. and Cavia aperea tschudii fitzinger)

Summary By light and electron microscopic observations intracellular fibrils were found in the adrenal medulla of adult wild (Cavia aperea tschudii) and domesticated guinea pigs (Cavia aperea f. porcellus). In certain cells of the adrenal medulla bundles of filaments can be traced from the perinuclear region into the periphery of the cells. Near the plasma membrane they split apart and attach to the desmosome-like regions. The individual filaments are about 70–100 Å in diameter. In adrenal medullary cells of chinchilla no fibrillar strands were observed, in wild and domesticated guinea pigs they occur in different numbers.

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Die Untersuchung wurde mit dankenswerter Hilfe der Deutschen Forschungsgemeinschaft durchgeführt.     

Hormone regulated enzyme activities of plasma membrane of decidual endometrium of the rat

Plasma membranes were purified from deciduoma of pseudopregnant rats and rat liver. Preparations contained 80% plasma membrane-derived material as based on electron microscope morphometry and analysis of enzyme markers. Several plasma membrane enzymes were tested for direct response to hormones. NADH-ferricyanide reductase of plasma membranes from both tissues was stimulated by glucagon and inhibited by insulin but was unresponsive to steroids. For steroids, responsiveness was limited to a reduction in NaF-stimulated adenylate cyclase activity by the steroid R5020. Thus, interaction of steroid hormones with plasma membranes, unlike that of glucagon and insulin, is not reflected in an altered activity of plasma membrane-bound dehydrogenases but may be exerted directly on adenylate cyclase.     

A simple method for mapping aquatic macrophytes

Aerial photography with a balloon-suspended camera is a suitable tool for surveying aquatic vegetation and for measuring water movements. Examples from the lake Lunzer Untersee (Austria) are given.     

Immuno-histochemical and -cytochemical Evidence Suggesting the Presence of Campylobacter jejuni and Campylobacter coli in Cases of Porcine Intestinal Adenomatosis

Antisera against a number of Campylobacter species were used in immuno-histochemical and -cytochemical studies on cases of porcine intestinal adenomatosis. Avidin-biotin-complex (ABC) and streptavidin immunoperoxidase methods were used on formalin-fixed, paraffin-embedded and frozen sections. Protein A gold method was used on formaldehyde fixed and frozen sections for immuno-cytochemistry. The antisera used were raised in rabbits by subcutaneous or intravenous injection of living or formalin treated organisms. Antisera against different serotypes of the thermotolerant, catalase positive Campylobacters, Campylobacter jejuni and Campylobacter coli gave positive reactions in the immuno-histochemical studies. The staining was found in intestinal epithelial cells both in the ileum and in the colon and was restricted to the apical cytoplasm of adenomatous epithelial cells. The staining had a granular pattern, the positive structures sometimes having the shape of Campylobacter. Epithelial cells in areas with normal differentiation of goblet cells did not stain. In contrast, no staining resulted with antisera against Campylobacter sputorum subsp. mucosalis and Campylobacter hyointestinalis. Immuno-cytochemistry, using antisera against Campylobacter jejuni showed that the positive staining in altered epithelial cells were restricted to intracellular organisms having a structure resembling Campylobacter spp.     

Localization and organization of phenol degradation genes ofPseudomonas putida strain H

The genetic organization of the DNA region encoding the phenol degradation pathway ofPseudomonas putida H has been investigated. This strain can utilize phenol or some of its methylated derivatives as its sole source of carbon and energy. The first step in this process is the conversion of phenol into catechol. Catechol is then further metabolized via themeta-cleavage pathway into TCA cycle intermediates. Genes encoding these enzymes are clustered on the plasmid pPGH1. A region of contiguous DNA spanning about 16 kb contains all of the genetic information necessary for inducible phenol degradation. The analysis of mutants generated by insertion of transposons and cassettes indicates that all of the catabolic genes are contained in a single operon. This codes for a multicomponent phenol hydroxylase andmeta-cleavage pathway enzymes. Catabolic genes are subject to positive control by the gene product(s) of a second locus.     

Effects of Nerve Growth Factor on Glutathione Peroxidase and Catalase in PC 12 Cells

Abstract: Nerve growth factor (NGF) is a member of the neuro- trophin family and is required for the survival and maintenance of peripheral sympathetic and sensory ganglia. In the CNS, NGF regulates cholinergic expression by basal forebrain cholinergic neurons. NGF also stimulates cellular resistance to oxidative stress in the PC12 cell line and protects PC12 cells from the toxic effects of reactive oxygen species. The hypothesis that NGF protection involves changes in antioxidant enzyme expression was tested by measuring its effects on catalase and glutathione per- oxidase (GSH Px) mRNA expression in PC12 cells. NGF increased catalase and GSH Px mRNA levels in PC 12 cells in a time- and dose-dependent manner. There was also a corresponding increase in the enzyme activities of catalase and GSH Px. Thus, NGF can provide cytoprotection to PC12 cells by inducing the free radical scavenging enzymes catalase and GSH Px.