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51.
52.
53.
Mg2+ restores membrane potential in rat liver mitochondria deenergized by Ca2+ and phosphate movements 总被引:1,自引:0,他引:1
Cellular ornithine biosynthesis could be expected to play a significant role in putrescine formation and hence in growth. Two enzymes are involved in ornithine biosynthesis: arginase and transamidinase. These enzyme activities were studied in two human melanoma cell lines differing in their Km of diamine oxidase for putrescine and in their tumorigenicity in nude mice. Arginase activity accounts for the majority of ornithine formed in the highly tumorigenic cell line, while the majority of ornithine is derived from transamidinase action in the poorly tumorigenic cell line, with concomitant formation of methyl guanidine, a potent inhibitor of diamine oxidase. 相似文献
54.
Stephen R. Sizemore R. David Cole 《In vitro cellular & developmental biology. Plant》1982,18(8):668-674
Summary The NMuMG cell line derived from normal mouse mammary epithelial cells was tested for responsiveness to hormones. The hormones
studied included insulin, glucocorticoids (cortisol and dexamethasone), and prolactin. In addition to membrane bound insulin
receptors and prolactin receptors, the cells had 2 × 104 cytoplasmic glucocorticoid receptors per cell. Morphological changes were observed in response to hormones. Clusters of cells
appeared with greatly increased diameter, and the number of cells per plate was reduced. The rate of DNA synthesis, corrected
by cell number, indicates that cell division, and hence cell turnover, was increased by the combination of all three hormones.
Insulin greatly enhanced protein synthesis, but glucocorticoid and prolactin did not further increase the rate. The combination
of the three hormones produced a change in the synthesis of histones, consistent with the increase in cell turnover.
There were substantial responses of enzyme activities to hormonal treatment of the cells. Insulin by itself induced a doubling
of the activity of glyceraldehyde phosphate dehydrogenase and perhaps a modest increase in NADH-cytochromec reductase. Lactose synthetase activity showed a three- to fourfold induction of both A and B subunits of the enzyme when
the cells were treated with insulin, glucocorticoid, and prolactin, and the effect of the latter two hormones was shown to
be additional to that of insulin.
This work was supported by Contract N01-CB-43866 from the National Cancer Institute, by Grants GB-38658 from the National
Science Foundation and GMS-20338 from the National Institutes of Health, and by the Agricultural Experimental Station at the
University of California. 相似文献
55.
James C. Fuscoe J.Patrick ONeill Richard Machanoff Abraham W. Hsie 《Mutation research》1982,96(1):15-30
We describe an assay for the quantification of reverse mutations at the hypoxanthine-guanine phosphoribosyltransferase (hgprt) locus in Chinese hamster ovary cells utilizing the selective agent L-azaserine (AS). Conditions are defined in terms of optimal AS concentration, cell density, and phenotypic expression time. After treatment, replicate cultures of 106 cells are allowed a 48-h phenotypic expression time in 100-mm plates. AS (10 μM) is then added directly to the growing culture and AS-resistant (ASr) cells form visible colonies. This assay is used to quantify ICR-191-, ICR-170-, and N-ethyl-N-nitrosourea-induced reversion of independently isolated HGPRT? clones. The ASr phenotype is characterized both physiologically and biochemically. All ASr clones isolated are stably resistant to AS and aminopterin but sensitive to 6-thioguanine. They also have re-expressed HGPRT enzyme. In addition, several revertants are shown to contain altered HGPRT. The data provide further evidence that ICR-191 and ICR-170 cause structural gene mutations in mammalian cells and also suggest that ICR-191, ICR-170, and N-ethyl-N-nitrosourea induce similar types of mutations in Chinese hamster ovary cells. 相似文献
56.
Stephen R. Cohen 《Journal of neurochemistry》1980,35(4):1008-1012
Concentrative influx of γ-aminobutyric acid (GABA) and α-aminoisobutyric acid (AIB) into incubated mouse cerebrum slices is decreased when pyruvate is substituted for glucose. Influx of GABA from pyruvate medium is not increased by presence of glucose, 2-deoxy-d -glucose (2-DOG), or 3-O-methyl-d -glucose (3-O-MeG). Influx of AIB is restored to the rate from glucose medium if 2-DOG is present initially, but is not restored if 2-DOG is added with AIB. Influx is not restored if 3-O-MeG is present initially, but is restored if 3-O-MeG is added with AIB. Influx is restored if glucose is present initially or is added with AIB. 相似文献
57.
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An EcoRI fragment, containing approx. 5100 base pairs (bp) of the immunity-end of bacteriophage Mu, was inserted into the multicopy plasmid pMB9 by in vitro recombination. The expression of early Mu genes, located on the cloned fragment, is thermo-inducible because of the presence of the ts mutation in gene c. The isolation of a transformant harbouring the recombinant plasmid, pGP1, was possible only when expression of Mu genes was prevented. pGP1 can be maintained at 28 degrees C at high copy number, but at 42 degrees C the pGP1 containing cells are killed due to the expression of the kil gene of Mu. The following Mu genes are present on pGP1: the ner gene, the integration and replication genes A and B, the cim gene, and the kil gene. pGP1 containing cells do not show Gam and Sot activity at 42 degrees C, therefore the leftmost EcoRI site on the Mu DNA is located between genes kil and gam or sot, or within the gam or sot gene. 相似文献
59.
60.
Anna Radomińska-Pyrek Maria Pilarska Piotr Zimniak 《Biochemical and biophysical research communications》1978,85(3):1074-1081
Phosphoethanolaminetransferase of high specific activity was solubilized from rat liver microsomes with the non-ionic detergent octyl glucoside. The solubilization method is fast and simple, allowing for processing of large amounts of material. The solubilized enzyme is stable. It contains virtually no phosphocholinetransferase activity. A preliminary characterization of the enzyme, with both diacyl- and alkylacyl-glycerol as substrate, is given. For the reaction, the lipid substrates were incorporated into artificial phospholipid bilayers (liposomes). 相似文献