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Biomedical subjects

T Schuster

Publications and source records attributed to T Schuster.

At least 91 records · Page 5Linked to original sources

Spinules in axospinous synapses of the rat dentate gyrus: changes in density following long-term potentiation.

Following high frequency stimulation of the perforant path the density of axospinous synapses from the middle third of the molecular layer of the rat dentate gyrus did not change significantly. By contrast, within this synaptic population the density of axospinous synapses containing synaptic spinules increased markedly. We interpret these results in terms of a structural modification related to enhanced synaptic efficacy.

Animals↗

[Tracheal compression by the brachiocephalic trunk in infants--surgical treatment of 30 cases].

This is a report on 30 cases of innominate artery compression of the trachea and its operative correction by an aorto-truncopexy. Tracheoscopy is the most important examination for arriving at the diagnosis. Magnetic resonance imaging (MRI), which offers representative pictures of many moments of expiration and inspiration, shows the anatomic relationship between the innominate artery, the aortic arch and the trachea, also demonstrating the extent of the tracheal compression. Surgical treatment is indicated if narrowing of the lumen of the trachea is greater than 70%. By fixing the aortic arch and the proximal innominate artery at the back of the sternum the trachea is relieved of its compression. In 30 children there was no unsuccessful operation, and none of them died.

Aorta, Thoracic↗

A conserved sequence in histone H2A which is a ubiquitination site in higher eucaryotes is not required for growth in Saccharomyces cerevisiae.

Histones H2A and H2B are modified by ubiquitination of specific lysine residues in higher and lower eucaryotes. To identify functions of ubiquitinated histone H2A, we studied an organism in which genetic analysis of histones is feasible, the yeast Saccharomyces cerevisiae. Surprisingly, immunoblotting experiments using both anti-ubiquitin and anti-H2A antibodies gave no evidence that S. cerevisiae contains ubiquitinated histone H2A. The immunoblot detected a variety of other ubiquitinated species. A sequence of five residues in S. cerevisiae histone H2A that is identical to the site of H2A ubiquitination in higher eucaryotes was mutated to substitute arginines for lysines. Any ubiquitination at this site would be prevented by these mutations. Yeast organisms carrying this mutation were indistinguishable from the wild type under a variety of conditions. Thus, despite the existence in S. cerevisiae of several gene products, such as RAD6 and CDC34, which are capable of ubiquitinating histone H2A in vitro, ubiquitinated histone H2A is either scarce in or absent from S. cerevisiae. Furthermore, the histone H2A sequence which serves as a ubiquitination site in higher eucaryotes is not essential for yeast growth, sporulation, or resistance to either heat stress or UV radiation.

Base Sequence↗

Neuroepithelial cell contacts in 12 days old rat embryo: normal and annulated gap junctions.

Neuroepithelial cells in the neural tube of 12 days old rat embryos make contact with each other by extended junctional complexes between their lateral membranes near the luminal surface. In this stage gap junctions are not numerous. Besides these "normal" gap junctions, especially in the upper part of the neuroepithelial cells, annulated gap junctions occur. They seem to originate by an endocytotic process of normal gap junctions with participation of cytoskeletal elements. The content of these annulated gap junctions mainly consists of ribosome-like particles in a high density, but larger particles may also occur. Annulated gap junctions sometimes reveal an intimate contact with the smooth endoplasmic reticulum or with the perinuclear cistern. If present in the perinuclear region the annulated gap junctions show membrane irregularities and other signs which are thought to mark steps of breakdown. Life-cycle and possible functions of the annulated gap junctions during neurulation need further investigation.

Animals↗

Proliferative potential of meningiomas determined with the monoclonal antibody Ki-67.

In 30 meningiomas we investigated the proliferation rate of various subtypes with the monoclonal antibody Ki-67. Frozen sections were incubated with Ki-67 antibody using a modified Alkaline Phosphatase anti-Alkaline Phosphatase (APAAP)-technique and evaluation of proliferation rate was done by cell counting. Meningiomas of the meningiotheliomatous, fibrous and angioblastic subtype without atypical histological findings contained 1% or less proliferating cells. In recurrent tumors, in transitional and in anaplastic meningiomas there is a marked increase of proliferating cells up to 20%. The distribution of marked cells varies in recurrent tumors and anaplastic meningiomas, and a focal proliferation of tumor cells was seen in meningiomas from transitional type. Immunohistological labelling of proliferating cells in meningiomas may allow a more precise prediction of the proliferation potential of each meningioma.

Alkaline Phosphatase↗

[Vesicle population of synapses in the hippocampus of the rat following early postnatal deprivation and administration of pyridostigmine].

Newborn male Wistar rats were subjected to early postnatal social and nutritional deprivation by separation of the pups from their mother animals from Day 3 to Day 14 for 16 hours daily. One group of the deprived animals was treated by daily injections of pyridostigmine (1 microgram/0.05 ml saline from Day 1 to Day 4, 5 micrograms/0.05 ml saline from Day 5 to Day 14). At the age of 14 days or 6 months, 5 deprived, 5 deprived and pyridostigmine treated rats and 5 controls were investigated. In the stratum radiatum of the hippocampal CA 1-region the vesicle population of axospinodendritic synapses was examined for quantitative ultrastructural changes using electron microscopic and morphometric methods. The vesicle density (number of vesicles/micron 2 terminal area) was determined in the whole presynaptic terminal as well as in distinct zones in the presynaptic terminal. 14 days of deprivation did not change the vesicle density in the whole presynaptic terminal, but did change the distribution of the vesicles. In 14 days old deprived rats the vesicle density was found to be decreased by about 10% in the presynaptic area bordering the synaptic contact zone (area 1), and it was increased by about 7% in the more distant area of the presynaptic terminal (area 2). Deprivation and simultaneous pyridostigmine treatment resulted in an elevated vesicle density in the whole presynaptic terminal by about 25%, in area 1 by about 8%, and in area 2 by about 30%. At the age of 6 months, the early postnatally deprived rats showed an increase in the vesicle density by about 8% in all areas of the presynaptic terminal when compared with the controls. Simultaneous pyridostigmine treatment led to a reduced vesicle density in the whole presynaptic terminal by about 5%, in area 1 by about 9%, and in area 2 by about 4%. The findings obtained following deprivation are interpreted as being the expression of an insufficient requirement of synaptic mechanisms caused by a lack of sensoric inputs during the early postnatal period. The results obtained in the neonatally pyridostigmine treated rats suggest permanent changes in the neurotransmitter metabolism following treatment with the psychotrophic drug. This may reflect a mechanism to compensate the effect of deprivation by neonatal pyridostigmine administration.

Animals↗

Yeast histone H2A and H2B amino termini have interchangeable functions.

The N-terminal ends of histones H2B and H2A have very different sequences and rates of evolution. However, they both extend from the nucleosome core and are positively charged. Short sequences at the C termini of both proteins also differ from each other and appear to be hydrophilic. Deletions at the N and C termini of yeast histones H2B2 and H2A1 do not obviously affect the cell's viability under normal growth conditions. However, deletions at the N termini of both H2B and H2A in the same cell are lethal or result in greatly reduced viability. Even switching portions of the N termini between H2B and H2A to create two chimeric histone proteins within the same cell has no obvious effect on viability. This supports the argument that the N-terminal end of one protein complements the function of the other.

Amino Acid Sequence↗

Organization, primary structure, and evolution of histone H2A and H2B genes of the fission yeast Schizosaccharomyces pombe.

The histone H2A and H2B genes of the fission yeast Schizosaccharomyces pombe were cloned and sequenced. Southern blot and sequence analyses showed that, unlike other eucaryotes, Saccharomyces cerevisiae included, S. pombe has unequal numbers of these genes, containing two histone H2A genes (H2A-alpha and -beta) and only one H2B gene (H2B-alpha) per haploid genome. H2A- and H2B-alpha are adjacent to each other and are divergently transcribed. H2A-beta has no other histone gene in close proximity. Preceding both H2A-alpha and -beta is a highly conserved 19-base-pair sequence (5'-CATCAC/AAACCCTAACCCTG-3'). The H2A DNA sequences encode two histone H2A subtypes differing in amino acid sequence (three residues) and size (H2A-alpha, 131 residues; H2A-beta, 130 residues). H2B-alpha codes for a 125-amino-acid protein. Sequence evolution is extensive between S. pombe and S. cerevisiae and displays unique patterns of divergence. Certain N-terminal sequences normally divergent between eucaryotes are conserved between the two yeasts. In contrast, the normally conserved hydrophobic core of H2A is as divergent between the yeasts as between S. pombe and calf.

Amino Acid Sequence↗

[Morphologic correlates of the electrical interactions between neurons in the limbic system].

Electron microscopical results on "special structural relations" between neighbouring neuronal elements (pericarya, dendrites) are demonstrated in different regions of the rat limbic system: field CA3 and field CA1 of the hippocamp, dentate gyrus, area entorhinalis (L V) and area retrosplenialis granularis (L III). The "special structural relations" are to be characterized as follows: direct apposition of membranes of the neighbouring neurons including an extracellular space of relatively constant width over a larger distance without neuroglia intervening this space. Areas of membrane appositions have been observed between neuronal somata ("soma-somatic appositions"), between dendrites ("dendro-dendritic appositions") and between both, somata and dendrites ("dendro-somatic appositions"). In the elmigraphs their length varied between 1 and 6 microns. In the entorhinal cortex and in the retrosplenial cortex soma-somatic appositions were in the majority, whereas in the hippocampal regions dendrodendritic appositions, in the dentate gyrus all types seem to be predominant. In the literature such direct appositions of neuronal membrane often have been described in the CNS of different species. They are considered as a possible morphological correlate of the ephaptic interaction, which is caused by field effects between neighbouring neurons. Following the literature the results of the ephaptic interactions vary between a weak facilitation and synchronous discharge of an unstimulated neuron by a stimulated one. Although such direct appositions are present in different groups of neurons in the limbic system, especially in the hippocamp, up to now their functional meaning is unclear. No correlation seem to exist between neuronal membrane appositions/ephaptic interactions and such a phenomenon like the hippocampal longterm potentiation; mechanisms of cooperativity included in the LTP like coactivation effects of pre- or postsynaptic elements still remain to be clarified.

Animals↗

Quantitative and morphological studies on the plasticity of mixed synapses as exemplified by clear, spherical vesicles.

Large mixed axosomatic synapses (synaptic membrane with chemically "active zones" and electric "gap-junction" parts) within the region of the oculomotor nucleus of the trout were stimulated for a prolonged period of time (14 days) under physiological conditions. Concerning the great number of clear vesicles that are found in the presynaptic part of this type of synapse it can be said that they can be subdivided morphometrically into two classes with respect to the special membrane complexes of the mixed synapse (active zone, gap junction). This paper is designed to find out to what an extent the proven adaptability of the "mixed synapse" system does reflect the quantitative changes in the population of these organelles. For this purpose the number (numerical density of vesicles NVv) as well as the size (vesicular volume Vv) of the vesicles were determined by stereologic methods from segments of vesicles that were visible in the electron microscopic picture. Stimulation of the contact caused an accumulation of vesicles in the presynaptic area of the active zone as well as in the region of the terminal axonal cylinder (myelin-free presynaptic part of the axon--"marginal zone"). At the gap junctions the number of vesicles remained unchanged, but their size diminished significantly. On the one hand, the findings obtained are discussed as an expression of potential compensatory mechanisms involved in vesicle supply or formation (axonal transport, recycling) for chemical transmission, and, on the other, as indicating possible interactions between vesicles and gap junctions for electric transmission. They suggest that the behaviour of the vesicle population of mixed synapses is governed by laws of its own.

Animals↗

Teleost Mauthner cap cells: intimate contact by gap junctions.

In rainbow trout the glial cap cells ensheating the Mauthner cell axon cap form a more or less double-layered arrangement consisting of fibrous astrocytes, sometimes intermingled with an oligodendrocyte. All cells of the glial wall are linked together by many gap junctions. Especially the somata of the astrocytes are connected to each other by large symmetrical gap junctions. For this reason the glial cap cells might act as an (electro-) physiological unity. Morphologically, the high axon cap resistance above all results from the densely packed glial elements. Regarding their function the astro-astrocytic gap junctions might contribute to the formation of this barrier.

Animals↗

Light-microscopic investigations on the problem of a dendritic bundling in the rat hippocampus.

Light-microscopic investigations were devoted to the arrangement of the apical dendrites of the pyramidal cells of the CA 1 and CA 3 fields and the subiculum in the hippocampus of adult rats. By means of sectional reconstructions, a dendritic bundling was found to occur in the above mentioned regions. The bundles of the CA 1 region, with a length of 50-80 microns, are detectable in the stratum pyramidale and in the transitional region to the stratum radiatum. They include 2-5, and in single cases up to 9, dendrites. The groupings of the apical dendrites of the CA 3 pyramidal cells, with a length of appr. 50 microns, extend from the stratum pyramidale into the stratum lucidum. The number of dendrites grouped together is larger than in the CA 1 region; a more pronounced row configuration of the dendrites in the bundle prevails. The formation of dendrite bundles is most pronounced in the subiculum: appr. 10 dendrites form 80 micron long units. Their appearance resembles that of the bundles known from the neocortex very closely. Referring to dendrodendritic membrane contacts (gap junctions or casual appositions), which allow an electrotonic coupling, and hence the development of a synchronous activity within the groups of neurons defined by the dendrite bundle, a possible functional significance of the bundles in the hippocampus is pointed out.

Animals↗

The estrogen-induced vitellogenin synthesis in chicken liver after estrogen withdrawal or antiestrogen treatment.

(1) The induction of vitellogenin synthesis in chicken liver by an estrogen implant as well as the decline of vitellogenin synthesis and nuclear receptor concentration after withdrawal of the implant were studied. For the detection of vitellogenin the SAC immunoprecipitation technique was used. The nuclear receptor decreases very rapidly and somewhat earlier than the capacity of the liver to synthesize vitellogenin. (2) The inhibition by antiestrogens of the estrogen-induced vitellogenin synthesis as well as of the accumulation of the estrogen-receptor complex in the nucleus was investigated. Tamoxifen as well as the recently described 1,1,2,2-tetramethyl-1,2-bis(4'-hydroxyphenyl)ethane were found to be true antiestrogens in the chicken liver, i.e. they inhibit estrogen-induced vitellogenin synthesis but themselves cause no induction.

Animals↗

Production and characterization of monoclonal antibodies against the Epstein-Barr virus membrane antigen.

Five murine hybridoma lines that produce monoclonal antibodies against Epstein-Barr virus membrane antigen (MA) were established. Immunoprecipitation experiments demonstrated that three of the antibodies precipitated both the 236,000 (236K) MA and the 212K MA. The other two antibodies precipitated the 86K MA. Antibodies against the 236K-212K MA and the 86K MA mediated complement-dependent cytolysis of Epstein-Barr-virus-infected cells. The antibodies against the 86K MA neutralized both the B95-8 and P3HR-1 viruses.

Antibodies, Monoclonal↗

[Electron microscopic and morphometric studies on the in vitro differentiation of mitochondria in neurons of hippocampus explant cultures as affected by orotic acid and sodium orotate].

The influence of orotic acid and sodium orotate on the differentiation of mitochondria of the neurons within explantate cultures of the hippocampus of 18 day old rat embryos was investigated by means of morphometrical and stereological methods. The ultrastructure of the mitochondria in controls and pharmacologically influenced cultures was analysed on electronmicrographs after 3, 13 and 20 days in vitro. According to their morphological appearance and state of preservation the mitochondria were classified in 3 types: juvenile mitochondria (stage I), active mitochondria (stage II) and destroyed mitochondria (stage III). After 3 days of cultivation the neurons in cultures treated with orotic acid and sodium orotate showed significantly higher rates in the numerical density of mitochondria (ratio of the number of all mitochondria per unit volume of cytoplasm) in comparison with controls. Moreover, sodium orotate treatment lead to a significant increase especially in the numerical density of the mitochondria of stage II (active mitochondria) on the third day in vitro. However, the mitochondrial volume per unit volume of cytoplasma of the neurons in drug influenced cultures is lower than in controls for each of these dates--3., 13., and 20. day in vitro. The volume of the mitochondria increased under treatment with sodium orotate from the 3. up to the 20. day of cultivation but never reached the values of the uninfluenced controls. The plastic changes of the mitochondria due to pharmacological treatment with RNA--precursors demonstrate the possibility of a stimulating effect of the drug on the differentiation of neuronal mitochondria in vitro.

Animals↗