Genetic polymorphism of lactate dehydrogenase isoenzymes in the carp (Cyprinus carpio) apparently due to a “null allele”

As a consequence of polyploidization, the carp is endowed with three genetic loci coding for LDH in most tissues (and additional ones in liver). However, each such duplicated gene may not be functionally essential for the organism and could be eliminated. In a population survey, an electrophoretic polymorphism was detected which may best be interpreted by the assumption of a null allele, which is apparently not subject to selective pressure. Thus this originally duplicated gene would have diverged in the course of evolution without the origin of differences in function, so that one or the other of the genes is dispensable.     

Dielectric properties of hemoglobin and myoglobin. I. Influence of solvent and particle size on the dielectric dispersion

Dielectric dispersion measurements with aqueous solutions of hemoglobin and myoglobin have been performed in the frequency range from 100 kcps to 15 Mcps. The influence of preparation, particle size, and solvent conditions was studied. The results are analyzed in terms of an orientational polarization mechanism.     

CONCENTRIC LAMINATION OF GLIAL PROCESSES IN OLIGODENDROGLIOMAS

Tissues were obtained by open biopsy of a series of human intracranial neoplasms, fixed in Veronal-buffered osmium tetroxide, and embedded in Vestopal-W. In two instances in which specimens were obtained from oligodendrogliomas in regions where the tumor had infiltrated but not entirely destroyed cortical tissues, glial processes were found to be arranged in a highly organized laminar fashion. This feature was not observed in two additional oligodendrogliomas nor in other types of intracerebral neoplasms. Three types of laminar structures were recognized: (a) perikaryal sheaths composed of several layers of overlapping or concentrically orientated glial processes, (b) layers of longitudinally orientated glial processes along the outer aspect of myelinated axons, and (c) small laminated figures composed of several concentrically disposed glial processes. Spirally constituted lamellar systems were not demonstrated. These findings indicate that under certain circumstances glial cells have the capacity to form sheaths and sheath-like structures by concentric lamination of several processes, rather than by spiraling of a single process.     

Über das Fehlen einer Beziehung zwischen dem Kaffeegenuß der Eltern und dem Geschlechtsverhältnis unter ihren Kindern

Ohne ZusammenfassungTeile dieser Arbeit wurden von Fräulein M. Kurth im Rahmen ihrer medizinischen Doktordissertation erarbeitet.Die Untersuchungen der Verfasser zum Mutationsproblem werden durch die Deutsche Forschungsgemeinschaft gefördert.     

Coated Vesicles in der Umgebung der neuro-muskulären Synapsen

Zusammenfassung In den verschiedenen Zellarten im Gebiet der neuro-muskulären Synapsen des mit OsO₄ fixierten Maus-Diaphragmas werden Mikropinozytose-Vesikel dargestellt, die durch eine besondere Membrandifferenzierung ausgezeichnet sind. Vorkommen, Feinstruktur und Entstehung dieser coated vesicles werden beschrieben. Ihre mögliche Funktion sowie die Bedeutung des Saumes werden in Zusammenhang mit der bereits vorliegenden Literatur diskutiert.

---

Summary Coated vesicles were demonstrated in various cell types in the region of the neuro-muscular junctions of the mouse diaphragm fixed with osmium tetroxide. These vesicles are characterized by a membrane which is specially differentiated. The occurrence, fine structure, and formation of these coated vesicles are described; their possible function and the nature of the coat are discussed in the light of existing literature.

---

---

Wir danken dem Schweizerischen Nationalfonds zur Förderung der wissenschaftlichen Forschung (Nr. 3806) für die Unterstützung dieser Arbeit.     

A Rapid Screening Test for Aflatoxin-synthesizing Aspergilli of the flavus-oryzae Group

A rapid test for the recognition of aflatoxin-synthesizing strains of the Aspergillus flavus–oryzae group is described. For this purpose the strains are cultivated on Czapek–Dox agar enriched with an aqueous extract of groundnuts, and in which sodium nitrate is replaced by ammonium chloride. Toxin production is observed by the production of a bright blue fluorescence in the medium when placed under an ultraviolet lamp.     

Pharmacologic evidence for the requirement of protein kinase C in IFN-induced macrophage Fc gamma receptor and Ia antigen expression.

Previous studies have implicated protein kinase C (PKC) as a mediator in the activation of macrophages by interferons. In order to probe further into the suspected role of protein kinase C in mouse peritoneal macrophage activation, the effects of protein kinase inhibitors in macrophage Fc gamma R and Ia Ag expression were studied. The protein kinase inhibitor, H7, reduced basal levels, and inhibited IFN-alpha-induced expression of Fc gamma R significantly. The concentration of H7 required to inhibit 50% of the Fc gamma R induction was approximately 12 microM, which reflects the previously reported affinity of this compound for PKC in vitro. H7 had only a minimal effect on IFN-gamma-induced Fc gamma R, suggesting different pathways of Fc gamma R induction by the two types of IFN. Ia induction by IFN-gamma was also inhibited by H7, indicating that both types of IFN can utilize PKC to mediate at least part of the signal required for Fc gamma R or Ia expression. HA-1004, a derivative of H7 which possesses high affinity for cyclic nucleotide-dependent protein kinases, but low affinity for PKC, did not alter induction, while H8, a slightly less effective PKC inhibitor than H7, was effective at higher concentrations. Another structurally distinct PKC antagonist, staurosporine, was also effective inhibiting IFN-alpha-induced Fc gamma R and IFN-gamma-induced Ia Ag expression, providing additional evidence that PKC is important. H7 was found to be effective when added as late as several hours after IFN treatment, indicating a prolonged or delayed requirement of PKC for optimal induction of Ia and Fc gamma R by IFN.