Experimentelle Zellkern-Verlagerung in Pilzhyphen

Zusammenfassung Die experimentelle Verlagerung der Zellkerne in vegetativen Hyphen von Basidiomyceten-Arten gelingt, ohne daß der Zelle Dauerschäden zugefügt werden.Die zur Teilung führenden extra- und intranucleären Prozesse können durch den mikrurgischen Eingriff unterbrochen werden, wenn dieser Eingriff in der Anfangsphase der Teilung erfolgt. Die Kernteilung ist jedoch nicht mehr aufzuhalten, wenn sie bereits weiter fortgeschritten ist. Es wird angenommen, daß die Kernteilungsprozesse mit der Auflösung der Kernmembran eingeleitet werden.Kernteilung und Einschmelzen der Altkernsubstanz müssen nicht äquilokal erfolgen. Die Kernteilung in der Schnalle verläuft normal, wenn die morphologisch distinkte Hauptmasse des teilungsbereiten Kernes mikrur gisch entfernt wird.Im Gefolge der Kernverlagerungen entstehen wachstumsfähige Zellen, die kernlos, ein- oder mehrkernig sein können.     

Elektronenmikroskopische Untersuchungen zur Dynamik neurosekretorischer Zellen von Enchytraeus (Oligochaeta)

Zusammenfassung Von lichtmikroskopischen Befunden der Neurosekretion bei dem Oligochaeten Enchytraeus ausgehend, haben wir an zwei elektronenmikroskopisch genau bezeichneten und festgelegten Zellen bzw. Zelltypen, die bereits lichtmikroskopisch charakterisiert worden waren, Untersuchungen über die submikroskopisch faßbare Zelldynamik durchgeführt. Die beiden Arten neurosekretorischer Zellen (Q-Zelle und P-Zellen) sind elektronen-mikroskopisch schon durch ihre Lage zu erfassen. Sie können nicht nur durch die Zellgröße, sondern auch durch ihre Elementargranula, den Aufbau des endoplasmatischen Retikulums und den Golgi-Apparat eindeutig unterschieden werden. Wie schon in den lichtmikroskopischen Untersuchungen wurde die Sekretionsaktivität mit der Amputation ausgelöst. Sowohl in der Q -als auch in der P-Zelle bewirkt die Amputation eine unmittelbare Sekretentleerung. Die darauf einsetzende Phase der Sekretproduktion ist submikroskopisch durch eine erhöhte Zahl von Golgistrukturen in diesen Zellen, durch das deutlich in Erscheinung tretende granuläre endoplasmatische Retikulum und durch eine fortschreitende Vergrößerung und Verdichtung von Lysosomen in beiden Zelltypen gekennzeichnet. Für die Q-Zelle sind weiterhin die Verstärkung des diesen Zelltyp besonders noch charakterisierenden Bereiches von Membranzisternen und die dortige Ribosomenbildung typisch. Auf Grund der Feststellungen wird die Frage der Beziehung einzelner Strukturen in diesen beiden Zelltypen zur Produktion des Neuro-sekrets diskutiert. Die elektronenmikroskopische Untersuchung führte zur Entdeckung eines weiteren Zelltyps, der im Lichtmikroskop bisher nicht erkannt worden war und der sich durch besonderen Reichtum an Mitochondrien und großen Lipoid (?)-Komplexen auszeichnet (M-Zelle). Über seine Bedeutung ist jedoch noch keine Aussage möglich.

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Summary The cytophysiology of two types of neurosecretory cells (Q and P cell) in the brain of the oligochete Enchytraeus was studied at the ultrastructural level. These cell types can be identified by their location, and particularly by the size difference of their elementary granules. Amputation of the last ten segments caused a release of secretory product followed by a phase of renewed production. This was characterized by changes in the endoplasmic reticulum, the Golgi apparatus, and the lysosomes. The role of these structures in the production of neurosecretory material was discussed. Furthermore, a cell type with extraordinarily numerous mitochondria, hitherto unknown in Enchytraeus, was described. Its function has not yet been determined.

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Mit Unterstützung durch die Sächsische Akademie der Wissenschaften zu Leipzig.

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Herrn Prof. Dr. F. Seidel, Marburg, zum 70. Geburtstag gewidmet.     

A new DNA marker (D4S90) is located terminally on the short arm of chromosome 4, close to the Huntington disease gene

Genetic linkage studies have mapped Huntington's disease (HD) to the distal portion of the short arm of chromosome 4 (4p16.3), 4 cM distal to D4S10 (G8). To date, no definite flanking marker has been identified. A new DNA marker, D4S90 (D5), which maps to the distal region of 4p16.3, is described. The marker was used in a genetic linkage study in the CEPH reference families with seven other markers at 4p16. The study, together with knowledge of the physical map of the region, places D4S90 as the most distal marker, 6 cM from D4S10. A provisional linkage study with HD gave a maximum lod score of 2.14 at a θ of 0.00 and no evidence of linkage disequilibrium. As D4S90 appears to be located terminally, it should play an important role in the accurate mapping and cloning of the HD gene.     

Histochemical demonstration of purine nucleoside phosphorylase (PNPase) in microglial and astroglial cells of adult rat brain

The histochemical localization of enzymes associated with purine nucleoside metabolism indicates that glial cells might participate in the regulation of these compounds in the central nervous system. In the present study we examined the histochemical localization of purine nucleoside phosphorylase (PNPase) in sections from adult rat brain. Some sections were also sequentially stained immunocytochemically for astroglial or microglial cells utilizing glial fibrillary acidic protein (GFAP) or OX-42 antibodies, respectively. Our observations showed that PNPase was restricted to glial cells, whereas neurons always remained negative. Brain sections stained for both PNPase and GFAP showed that the GFAP-positive astroglial cells were always PNPase positive. Other PNPase-positive but GFAP-negative cells were also observed. These cells resembled microglial cells, and brain sections reacted for both PNPase and OX-42 confirmed this by showing that the major part of OX-42-positive microglial cells were PNPase positive. In these sections, the PNPase-positive but OX-42-negative cells present resembled astroglial cells. From our double staining experiments, we conclude that PNPase is present in both astroglial and microglial cells in normal adult brain.     

Clinical and biochemical studies in three patients with severe early infantile Cockayne syndrome

Summary We present clinical and biochemical data from three patients with severe Cockayne syndrome (CS) of very early onset. Unlike in classic CS, signs became evident in the first weeks of life and led to unusually early death. Fibroblasts from two of the patients showed a complete defect of the repair of UV-induced thymine dimer lesions. They were unable to remove thymine dimer lesions from their DNA, had a severe reduction of the RNA synthesis rates after UV irradiation, and showed no reactivation of an UV-inactivated indicator gene and no DNA recondensation after UV irradiation. DNA repair investigated in these two fibroblast cell strains resembled that of xeroderma pigmentosum cells of complementation group A. In contrast, fibroblasts from the third patient showed the same in vitro repair characteristics as classic CS cells.     

Human glomerular mesangial cells inactivate leukotriene B4 by reduction into dihydro-leukotriene B4 metabolites

Due to its potent chemotactic properties leukotriene B4 is an important mediator of inflammatory reactions. Cultured human kidney mesangial cells converted exogenously added leukotriene B4 efficiently into three different more lipophilic metabolites, two of them probably representing dihydro-leukotriene B4 isomers. This represents an alternative metabolic pathway, in contrast to leukotriene B4 omega-oxidation found in human polymorphonuclear leukocytes. Both dihydro-leukotriene B4 isomers had nearly completely lost their ability to induce leukocyte chemotaxis as compared to leukotriene B4.     

Scavenging of Hydrogen Peroxide in the Endosperm of Ricinus communis by Ascorbate Peroxidase

The fat-storing endosperm of Ricinus communis L. was found tocontain an ascorbate peroxidase (EC 1.11.1.11 [EC] ), which is nearlyas active as catalase (EC 1.11.1.6 [EC] ) in degradation of hydrogenperoxide (H₂O₂) at its physiological concentrations. This ascorbateperoxidase probably functions together with monodehydroascorbatereductase (EC 1.6.5.4 [EC] ) or dehydroascorbate reductase (EC 1.8.5.1 [EC] )and glutathione reductase (EC 1.6.4.2 [EC] ) to remove the H₂O₂ producedduring the transformation of fat to carbohydrate in the glyoxysomes.The activities of these enzymes as well as the content of ascorbateand glutathione increase parallel to the activities of glyoxysomalmarker enzymes during the course of germination. Inhibitionof catalase by aminotriazole results in increases of the ascorbateperoxidase activity and of the glutathione content. All fourenzymes are predominantly localized in the cytosol of the Ricinusendosperm with low activities found in the plastids and themitochondria. The results suggest, that the ascorbate-dependentH₂O₂ scavenging pathway, which has been shown to be responsiblefor the reduction of photosynthetically derived H₂O₂ in thechloroplasts, operates also in the Ricinus endosperm. (Received June 5, 1990; Accepted July 31, 1990)