Conversion ofβ-mercaptopyruvate to 2-mercaptoethanol by yeast enzymes

Zusammenfassung Hefeextrakt decarboxyliert-Mercaptobrenztraubensäure zu 2-Mercaptoazetaldehyd, welches von DPNH und Alkohol-Dehydrogenase zu 2-Mercaptoethanol reduziert wird. Enzymatische und chemische Messungen bestätigen den Reaktionsmechanismus.

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Supported by grants of the USPH, C-4681 and C-3211, and by a grant of the American Heart Association Inc., New York.     

17β-Estradiol-sensitivity of cultured myometrial cells

Summary The estrogen sensitivity of cells cultured from the rat myometrium was studied by growing the cells in the absence or presence of 1 nM 17-estradiol. Following a time lag of 10 days, exposure to estrogen resulted in increased incorporation of radiothymidine by the cells. Estrogen treatment also decreased isoproterenol-dependent and GTP-dependent adenylate cyclase activity, but had no effect on basal activity. These cultured cells have been shown previously to have some properties of uterine smooth muscle. The effects estrogen has in viyro, therefore, may reflect important properties in vivo that account for the mechanism by which the sex steroid decreases the sensitivity of the myometrium to isoproterenol.     

β-Adrenergic stimulation of androgen production by fetal mouse Leydig cells in primary culture

Summary The responsiveness of fetal mouse Leydig cells to catecholamines (epinephrine, norepinephrine), a-agonist agent (L-isoproterenol) and hCG was investigated in vitro. Fetal Leydig cells when freshly isolated were unable to respond to L-isoproterenol (10^–5M). However, L-isoproterenol, epinephrine and norepinephrine significantly stimulated androgen production by fetal Leydig cells after 24 h of primary culture. Androgen production was increased in both conditions and to a greater extent by hCG. Propranolol blocked the stimulatory effect of L-isoproterenol and epinephrine. It is concluded that catecholamines can regulate fetal testosterone biosynthesis.     

Activation of cytotoxic T cells by solid tumours?

Tumour-specific cytotoxic T cells (CTLs) are among the best-defined biological anticancer weapons. Nevertheless, they often fail to control tumour growth in vivo. Many reasons for this have been evoked tumours may actively inhibit CTLs, or may protect them selves from CTL recognition by various means. However, one does not necessarily need to postulate such active immune evasion mechanisms specifically acquired by tumour cells. In this review we argue that the failure of immune protection is due to the intrinsic inability of tumours to activate an effective immune response, and that many tumours are similar to normal issues in this respect. It is striking to see that the majority of the so-called immune escape mechanisms are not specifically acquired by selected tumour cells, but are common mechanisms shared between solid tumours and normal, healthy tissues. Immune responses are poor because tumour antigens do not efficiently localize to lymph follicles in lymphoid tissues, and are not efficiently presented to CTLs in an immunogenic context. The fact that tumours do not induce CTLs but are often susceptible to lymphocyte-mediated cytotoxicity indicates that more intensified immunization protocols should result in improved clinical outcome.     

The influence of N-methyl-N-β-chloroethyl hydrazines on the mitotic index of Ehrlich ascites tumor cells and the leukopoiesis of the mouse

Summary The cytostatic activity of N-methyl-N--chloroethylbenzaldehyd hydrazone, (B1) is at least equal to that of procarbazine when its effect is tested with the Ehrlich ascites tumor cells of the mouse and the Yoshida sarcoma of the rat. B1 causes a slighter decrease of mitotic cells and no shift from prophase to metaphase. These results suggest that the cytostatic effect of B1 is due to interference with cell metabolism or an effect at the cell membrane and not to an effect on cell proliferation. This assumption is supported by a considerable depression, of lymphocytes and a minor effect on granulopoiesis, which is especially sensitive towards proliferation toxins. All these findings suggest a different mechanism of action of B1 and procarbazine.     

Antagonism of chlorpromazine byβ-melanocyte stimulating hormone (β-MSH)

Résumé Une préparation hautement purifiée de l'hormone mélanophorétique-MSH inhibe les effets de la chlorpromazine au niveau de la moelle spinale.     

The effect of ischæmia on nucleoproteins in liver cells

Résumé Chez la souris, 24 heures après la ligature du pédicule d'un lobe hépatique, la basophilie cytoplasmique disparaît alors que les noyaux conservent une colorabilité normale par la méthode deFeulgen. Les dosages chimiques établissent que le taux de l'acide ribonucléique s'abaisse considérablement, tandis que celui de l'acide désoxyribonucléique ne subit pas de modifications appréciables. Ces phénomènes sont liés à la destruction des granules et microsomes séparables par ultracentrifugation. Une partie de ces nucléoprotéines se retrouve, après ultracentrifugations répétées, dans le liquide surnageant.     

Selective protection of cells against X-irradiation. Isoproterenol protects only those cells that possesβ-adrenoreceptors

Summary In mixed culture of Chinese hamster fibroblatst, clone 431, and transformed murine L fibroblasts, clone B-82, isoproterenol was found to protect only 431 cells against ionizing radiation. It was shown that 431 cells, in contrast to B-82 cells, possess-adrenoreceptors, and the radioprotective effect of isoproterenol can be realized only if this agent interacts with-adrenoreceptors coupled with the cAMP system. Since malignization often causes the disappearance of-adrenergic and other hormone receptors, the combined culturing and irradiation of the cells studied can be regarded as a model of the growth of malignant cells (B-82) among normal tissue cells (431 cells) under conditions of radiation therapy. A possibility of selective protection against radiation damage of normal tissue cells, with retention of the former radiosensitivity of tumor cells, is discussed.     

The adoption of self-induction by telephony, 1886–1889

Through 1886 to 1889 understanding of the mechanism of telephone transmission was transformed from an electrostatic and traditional view to an electrodynamic one conforming with Maxwell's scheme. Observed at the level of commercial application this painful adjustment occurred via a sequence of controversies connected with self-induction—on techniques of telephony, on electrical measurement, on lightning conductors and on matters of professional ethics—in which the parts played by evidence, by theory, and by authority were strangely mixed. The well-known confrontation of O. Heaviside and W. H. Preece was at the centre of the debate. An open division between traditionalists and progressives amongst electrical engineers was provoked, and the effectiveness of mathematical theory as against pure pragmatism at the practical level had in the end to be conceded.     

The microbiological dehydrogenation of 16β-methyl-5α-dehydrocortisone

Zusammenfassung Über die mikrobiologische Umwandlung des 16-Methyl-5-Dehydrocortisons in 16-Methylprednison durch einen Stamm vonCorynebacterium simplex wird berichtet. Mit Hilfe dieser Bakterienkulturen ist es möglich, in relativ kurzer Zeit die beiden Doppelbindungen in den Stellungen 1 und 4 im A-Ring des 16-Methylprednisons einzuführen.     

The structure of human interferon-β: implications for activity

Interferons (IFNs) are potent extracellular protein mediators of host defence and homoeostasis. This article reviews the structure of human IFN-β (HuIFN-β), in particular in relation to its activity. The recently determined crystal structure of HuIFN-β provides a framework for understanding of the mechanism of differentiation of type I IFNs by their common receptor. Insights are generated by comparison with the structures of other type I IFNs and from the interpretation of existing mutagenesis data. The details of the observed carbohydrate structure, together with biochemical data, implicate the glycosylation of HuIFN-β, which is uncommon among type I IFNs, as an important factor in the solubility, stability and, consequently, activity of the protein. Finally, these structural implications are discussed in the context of the clinical use of HuIFN-β. Received 12 June 1998; received after revision 16 July 1998; accepted 16 July 1998     

The effect ofβ-aminopropionitrile (BAPN) on bacteria

Zusammenfassung Alle untersuchten Bakterien waren gegenüber BAPN entweder ganz unempfindlich oder zeigten nur eine unspezifische Wachstumsverminderung. Diese Bakterien scheinen zum Studium lathyrogenischer Substanzen ungeeignet. Die Annahme, dass BAPN auf Mucopolysacchariden wirkt, konnte durch diese Untersuchung nicht gestützt werden.

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This work was supported by Research Grant A-4002 from the National Institute of Arthritis and Metabolic Diseases, U.S. Public Health Service. We are also grateful to Abbott Laboratories, North Chicago (Illinois) for generous gifts of mono--aminopropionitrile (BAPN) fumarate.     

Microbiological transformations ofβ-sitosterol and stigmasterol by a soil pseudomonad

Summary Fermentation of -sitosterol by a soil pseudomonad resulted in the formation of 4-stigmasten-3-one, 4-stigmasten-3-one-6-ol and 5-stigmasten-3, 7-diol. In case of stigmasterol the metabolites isolated and characterized were 4,22-stigmastadien-3-one, 4, 22-stigmastadien-3-one-6-ol and 5,22-stigmastadien-3, 7-diol.The soil pseudomonad strain (BS-305) is maintained at 4°C on nutrient-agar slants.     

Interferon-β can induce the production of plasminogen activator by cultured human cancer cells

Summary Three cultured human cell lines, renal cancer cells (ACHN), bladder cancer cells (EJ), and fibroblasts transformed in culture by Co-60 gamma rays (KMST-6), when treated with interferon-, produced 1.5 to 4 times as much plasminogen activator as the untreated control cultures. This enhanced production of PA was inhibited by cycloheximide or actinomycin D.     

Targeting mitochondria by α-tocopheryl succinate kills neuroblastoma cells irrespective of MycN oncogene expression

Amplification of the MycN oncogene characterizes a subset of highly aggressive neuroblastomas, the most common extracranial solid tumor of childhood. However, the significance of MycN amplification for tumor cell survival is controversial, since down-regulation of MycN was found to decrease markedly neuroblastoma sensitivity towards conventional anticancer drugs, cisplatin, and doxorubicin. Here, we show that a redox-silent analogue of vitamin E, α-tocopheryl succinate (α-TOS), which triggers apoptotic cell death via targeting mitochondria, can kill tumor cells irrespective of their MycN expression level. In cells overexpressing MycN, as well as cells in which MycN was switched off, α-TOS stimulated rapid entry of Ca(2+) into the cytosol, compromised Ca(2+) buffering capacity of the mitochondria and sensitized them towards mitochondrial permeability transition and subsequent apoptotic cell death. Prevention of mitochondrial Ca(2+) accumulation or chelation of cytosolic Ca(2+) rescued the cells. Thus, targeting mitochondria might be advantageous for the elimination of tumor cells with otherwise dormant apoptotic pathways.     

The problem of ‘conditioning’ the action of antiphlogistic corticoids by the thyroid gland

Zusammenfassung Experimentell wurde die Wirkung von Prednison und Hydrocortisonacetat auf die Entwicklung des Fremdk?rpergranuloms an intakten und an thyreoid- und parathyreoidektomierten Tieren untersucht. Nach beidseitiger Thyreoidektomie konnte keine Unterdrückung der entwicklungshemmenden Effekte der Corticoide festgestellt werden.      

The presence of RNA of the A–U type in citrate nuclei isolated from rabbit liver cells

Zusammenfassung Die in 5% iger Zitronensäure isolierten Kaninchenleberkerne enthalten eine minimale Fraktion von RNS, die sich durch ihren Gehalt an Basen der DNS annähert (A+U/G+C>1). Diese RNS wird während der Extraktion mit dem 6% igen Natrium-p-Amino-salicylat und dem Phenol zusammen mit der DNS und RNS vom G+C-Typ gewonnen.     

The potential importance of myeloid-derived suppressor cells (MDSCs) in the pathogenesis of Alzheimer’s disease

The exact cause of Alzheimer’s disease (AD) is still unknown, but the deposition of amyloid-β (Aβ) plaques and chronic inflammation indicates that immune disturbances are involved in AD pathogenesis. Recent genetic studies have revealed that many candidate genes are expressed in both microglia and myeloid cells which infiltrate into the AD brains. Invading myeloid cells controls the functions of resident microglia in pathological conditions, such as AD pathology. AD is a neurologic disease with inflammatory component where the immune system is not able to eliminate the perpetrator, while, concurrently, it should prevent neuronal injuries induced by inflammation. Recent studies have indicated that AD brains are an immunosuppressive microenvironment, e.g., microglial cells are hyporesponsive to Aβ deposits and anti-inflammatory cytokines enhance Aβ deposition. Immunosuppression is a common element in pathological disorders involving chronic inflammation. Studies on cancer-associated inflammation have demonstrated that myeloid-derived suppressor cells (MDSCs) have a crucial role in the immune escape of tumor cells. Immunosuppression is not limited to tumors, since MDSCs can be recruited into chronically inflamed tissues where inflammatory mediators enhance the proliferation and activation of MDSCs. AD brains express a range of chemokines and cytokines which could recruit and expand MDSCs in inflamed AD brains and thus generate an immunosuppressive microenvironment. Several neuroinflammatory disorders, e.g., the early phase of AD pathology, have been associated with an increase in the level of circulating MDSCs. We will elucidate the immunosuppressive armament of MDSCs and present evidences in support of the crucial role of MDSCs in the pathogenesis of AD.