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K Kohno

Publications and source records attributed to K Kohno.

At least 415 records · Page 23Linked to original sources
PubMed1988

On the glutamate transport through cell envelope vesicles of Halobacterium halobium.

Glutamate uptake by envelope vesicles of Halobacterium halobium was measured. Previous authors showed that the glutamate uptake needs the illumination as well as Na+ gradient across the membrane. The latter is considered to be the driving force for the uptake. No satisfactory explanation for the necessity of the illumination has not been given. We found that in the absence of Cl- in the medium, only Na+ gradient was enough to induce the glutamate uptake, i.e. no illumination was needed. Glutamate uptake was measured with various strains of H. halobium. We found that the envelope vesicles prepared from strains containing no bacteriorhodopsin showed the glutamate uptake in the dark and in the presence of Cl- in the medium provided only that Na+ gradient is imposed.

Cell Membrane↗
PubMed1988

Complete nucleotide sequence and characterization of the 5'-flanking region of mammalian elongation factor 2 gene.

The hamster elongation factor 2 gene was isolated from genomic libraries of diphtheria toxin- and Pseudomonas aeruginosa exotoxin A-resistant cells containing non-ADP-ribosylatable elongation factor 2, and its structure was determined by a combination of restriction endonuclease mapping and DNA sequence analysis. The entire gene is about 6 kilobases long and has 13 exons. Almost all the introns are about 90-200 bases long, except the first and third, which are about 1 kilobase and 400 bases long, respectively. The first exon is processed just after the initiation codon for translation. The promoter of this gene was also characterized. As this gene contains the mutation conferring resistance to diphtheria toxin and P. aeruginosa exotoxin A, introduction of this gene into mammalian cells results in expression of toxin resistance. Using this characteristic, gene expression by deletion mutants of the 5'-flanking region were examined, and results showed that about 60 base pairs upstream of the TATA sequence were most efficient for expression of the elongation factor 2 gene.

Amino Acid Sequence↗
PubMed1988

Ultrastructural study on the meninx of the goldfish brain.

The cranial meninges of the goldfish were studied by means of transmission electron microscopy combined with the freeze-fracturing technique. The goldfish has three cranial meninges. The outer layer consists of flattened cells, which are stratified in 3 to 7 layers and are packed densely with many interdigitations of cell processes. The constituent cells in the outer layer have copious smooth endoplasmic reticulum and are joined by gap junctions but have no desmosomes. The intermediate layer is thin, continuous, and single cell. In the replicas, both the upper and the lower surfaces of the intermediate layer cells have numerous openings of pinocytotic vesicles, but the upper surface is characterized by round gap junctions, whereas the lower surface is identified by a linear continuation of a combination of tight junctions and gap junctions and by desmosomes. The lateral surface has a hexagonal network of tight junctions and gap junctions with internally located desmosomes, which functions as a barrier to intercellular movement of lanthanum. The inner layer consists of a meshwork of reticular cells and large intercellular spaces, in which fine granular material, capillaries, and different types of blood-derived free cells can be found. Cells in the inner layer contain rough endoplasmic reticulum stacked in lamellae and have irregular processes joined by desmosomes. The goldfish meninges are compared with the meninges of mammals.

Animals↗
PubMed1988

Potentiation by a biscoclaurine alkaloid, cepharanthine, of the toxicity of conjugates of epidermal growth factor with Pseudomonas exotoxin in HeLa cells.

Cepharanthine, a biscoclaurine alkaloid, causes an 8-fold enhancement of the cytotoxic effect of a conjugate of epidermal growth factor (EGF) coupled with Pseudomonas exotoxin in HeLa cells. Cepharanthine also potentiates the effect of Pseudomonas exotoxin. Cepharanthine does not affect the binding and uptake of 125I-EGF by HeLa cells, but it delays the release of radioactivity associated with 125I-EGF into the medium. Analysis by colloidal silica gradients using cell homogenates suggests that 125I-EGF accumulates in the lysosomes of cells treated with cepharanthine and that [3H]cepharanthine accumulates in lysosomes. The pH in HeLa cell lysosomes is 5.2, and cepharanthine does not significantly increase the pH. Electron microscopy shows an increased number of electron-dense bodies and dilated Golgi apparatus after cepharanthine treatment. Cepharanthine appears to accumulate in lysosomes, and it may delay degradation of EGF-Pseudomonas exotoxin in the cells as does 125I-EGF.

ADP Ribose Transferases↗
PubMed1988

Bioavailability and pharmacokinetics of oral dopamine in dogs.

The bioavailability and pharmacokinetics of oral dopamine (DA) were studied in dogs. Plasma concentrations of DA and its main metabolites, such as dopamine-3-O-sulfate (DA-SO4) and 3,4-dihydroxyphenyl acetic acid (DOPAC) were determined after intravenous or oral administration of DA using high-performance liquid chromatography with electrochemical detector (HPLC-ECD). Following the intravenous administration, plasma DA-SO4 and DOPAC concentrations were lower than the plasma DA concentration. On the other hand, following the oral administration, plasma DA-SO4 and DOPAC concentrations were much higher than the plasma DA concentration. The absolute bioavailability of DA after oral administration was calculated to be approximately 3%. Intraduodenal and mesenteric venous administration of DA revealed that DA-SO4 was mainly produced in the intestine and DOPAC was produced in the intestine and liver. On the basis of these observations, the bioavailability and pharmacokinetics of oral DA are discussed in connection with the metabolic inactivation due to first-pass metabolism.

3,4-Dihydroxyphenylacetic Acid↗
PubMed1988

The pattern of distribution of serotoninergic fibers in the anterior horn of the chick spinal cord.

The pattern of distribution of serotonin positive fibers in the motor nuclei of the chick spinal cord was examined immunohistochemically by using an antiserum against serotonin. A dense aggregation of serotoninergic fibers was located around anterior horn cells in the cervical spinal cord. In the brachial spinal cord, serotoninergic fibers were densely aggregated in the medial motor column and in the parts of the lateral motor column. There were two regions of serotonin immunoreactivity in the lateral motor column of the brachial spinal cord; one located in the ventromedial regions where a dense aggregation of serotoninergic fibers was found, and the reminder of the lateral motor column where only a few serotoninergic fibers were observed. The region containing a dense cluster of serotoninergic fibres around profiles of motoneuron somata and proximal dendrites appears to correspond to motor neuron pools of flexor muscles. In the thoracic spinal cord a high density of serotoninergic fibers was found in the motor nucleus. In the lumbosacral spinal cord (segments LS1-LS8) serotoninergic fibers were not observed in the medial motor column. However, there were five regions in the lateral motor column, where a high density of serotoninergic fibers was found. These very likely correspond to motor neuron pools of muscles which extend the hip joint.

Animals↗
PubMed1988

Lateral bud outgrowth on decapitated shoots of low-pruned mulberry (Morus alba L.).

After decapitation, lateral shoot growth of mulberry coppice (Morus alba L. cv. Shin-ichinose) from 10-year-old stumps had an extremely acrotonic form compared with that of intact one-year-old stems of trees during the spring. When one dominant shoot from each stump was decapitated, only a few upper lateral buds grew out and elongated. Defoliation of the decapitated shoots resulted in an increase in the number of shoots sprouting and a decrease in the rate of elongation of the laterals. Further enhancement of laterals on decapitated dominant shoots resulted from the removal of competing intact coppice shoots from the stumps. 1-Naphthaleneacetic acid (NAA) applied as a spray reduced the number of lateral buds sprouting from both defoliated, decapitated erect shoots and intact horizontally trained shoots. The results suggest that management of mulberry coppice could increase the supply of leaves for commercial silk production.

Journal Article↗
PubMed1988

Estrogen inhibits the growth of MCF-7 cell variants resistant to transforming growth factor-beta.

Human breast cancer MCF-7 cells containing estrogen receptor are killed by transforming growth factor-beta (TGF-beta). We isolated variants of MCF-7 highly resistant to TGF-beta. Variants ES-1 and ES-4 were cloned, and the growth of ES-1 and ES-4 was found to be inhibited by estradiol, whereas estradiol stimulated the growth of the parental MCF-7 cells. ES-1 cells contained about 2-fold higher level of estradiol receptor than MCF-7 cells. Addition of estradiol to the culture medium for MCF-7 and the variant changed the expression of several secreted proteins. The repertoire of secreted proteins was markedly altered in the variant. Polypeptides of molecular weight 52,000 (52 K), 65 K and 160 K were increased about 10- to 50-fold in both estradiol-treated MCF-7 and ES-1 cells. Polypeptide of 130 K was decreased in estradiol-treated ES-1 cells while this polypeptide was increased about 4-fold in estradiol-treated MCF-7, as compared with untreated MCF-7. Polypeptide of 100 K was specifically secreted in ES-1 whether or not estradiol was present, but there appeared to be no significant amount of the 100 K protein in MCF-7. The estradiol-hypersensitive phenotype is discussed in relation to its aberrant expression of secreting proteins.

Breast Neoplasms↗
PubMed1988

Vincristine-resistant human cancer KB cell line and increased expression of multidrug-resistance gene.

A multidrug-resistant clone of human cancer KB cells was isolated by stepwise selection on exposure to increasing doses of vincristine. The final clone, VJ-300, obtained after ethylmethane sulfonate mutagenesis showed 400-fold higher resistance to vincristine than did KB cells. Cellular accumulation of vincristine in VJ-300 was decreased to less than one-tenth of that in KB. The cells were also cross-resistant to daunomycin, adriamycin, actinomycin D, colchicine and VP-16. During continuous culturing in the absence of any drug for several months, a different colchicine-resistant and multidrug-resistant clone, KB-C1, reverted almost completely to drug sensitivity, whereas drug resistance in VJ-300 was stably maintained. Amplification of the multidrug-resistance-1 (mdr-1) gene was more than 20-fold in KB-C1, but less than 2-fold in VJ-300. mdr-1 mRNA was, however, expressed in VJ-300 at a rate comparable to KB-C1. Acquisition of high multidrug resistance in VJ-300 might be correlated with both activated transcription of mdr-1 gene and amplification.

ATP Binding Cassette Transporter, Subfamily B, Mem↗
PubMed1987

Highly frequent single amino acid substitution in mammalian elongation factor 2 (EF-2) results in expression of resistance to EF-2-ADP-ribosylating toxins.

Toxin-resistant polypeptide chain elongation factor 2 cDNA has been cloned from a mutant hamster cell line with only non-ADP-ribosylatable elongation factor 2. The mutation conferring resistance to diphtheria toxin and Pseudomonas aeruginosa exotoxin A is a G-to-A transition in the first nucleotide of codon 717. Codon 715 encodes a histidine residue that is modified post-translationally to diphthamide, which is the target amino acid for ADP-ribosylation by both toxins. Transfection of mouse L cells with a recombinant elongation factor 2 cDNA differing from the wild-type only by this G-to-A transition confers resistance to P. aeruginosa exotoxin A. The degrees of toxin-resistant protein synthesis of stable transfectants are dependent on the ratio of non-ADP-ribosylated elongation factor 2 to wild-type elongation factor 2, not the amount of non-ADP-ribosylated elongation factor 2. The mutation creates a new Mbo II restriction site in the elongation factor 2 gene. Several independently isolated diphtheria toxin-resistant Chinese hamster ovary cell lines show the same alteration in the Mbo II restriction pattern.

ADP Ribose Transferases↗
PubMed1987

Pharmacokinetic analysis of concentration data of drugs with irregular absorption profiles using multi-fraction absorption models.

Nonlinear regression analysis of plasma drug concentration data with irregular or stepwise absorption profiles was studied using multi-fraction absorption models in which drugs in the gastrointestinal tract were assumed to be divided into several fractions each with its respective lag time and absorption rate constant. Plasma allopurinol concentration data, with two-phase absorption profiles in dogs after oral administration, were found to be satisfactorily fitted using a two-fraction absorption model. Plasma sulfisoxazole concentration data in humans were also successfully analyzed using a two-fraction absorption model. Plasma and urinary concentrations of pindolol in humans after oral administration of sustained-release preparations were fitted to two- or three-fraction absorption models. The pharmacokinetic absorption behavior of a sustained-release preparation of diltiazem hydrochloride was studied using a multi-fraction absorption model. Pharmacokinetic parameters derived from these models and those from the discontinuous absorption model were compared.

Allopurinol↗
PubMed1987

The topographical organization of neurons in the dorsal hypothalamic area that project to the spinal cord or to the nucleus raphé pallidus in the rat.

The present study was undertaken using retrograde labeling techniques to clarify whether the neurons in the dorsal hypothalamic area (DHA) that project to the spinal cord are the same as those that project to the nucleus raphé pallidus (NRP). Following an injection of wheat germ agglutinin-conjugated horseradish peroxidase (WGA-HRP) in the NRP many labeled small neurons (6-13 X 9-22 microns) with an oval shape were found in the ventromedial part of the DHA. At the level of the dorsomedial hypothalamic nucleus, they formed a distinct and compact cell cluster. Labeled neurons, which were large in size (9-22 X 11-36 microns) with oval and triangular shapes, were found mainly in the dorsolateral part of the DHA after injections of horseradish peroxidase (HRP) in the spinal cord. In a double-labeling experiment, Fast Blue or True Blue, and Nuclear Yellow were injected in the NRP and in the spinal cord, respectively. A large number of blue-fluorescent neurons were located mostly in the ventromedial part of the DHA, while yellow-fluorescent ones were found in the dorsolateral part of the DHA. However, no double-labeled neurons were found in the DHA. These results show that the neurons of the DHA projecting to the NRP are essentially different from those which project to the spinal cord.

Animals↗
PubMed1987

Accessory cell function in a Con A response: role of Ia and interleukin 1.

Accessory cell (A-cell) function in a Con A response was analyzed. Irradiated P388D1 cells efficiently induced a proliferative response to Con A of T cells purified from spleen cells, whereas paraformaldehyde-fixed P388D1 cells failed to serve as A cells. Although IL-1 containing culture supernatant (SN) of a macrophage hybridoma induced the Con A response of the T-cell preparations, the depletion of Ia+ cells by the treatment with anti-Ia antibody and complement abrogated the response in the presence of IL-1. Fixed P388D1 cells and the hybridoma SN synergized in the reconstitution of the response. A 15,000-Da fraction of the hybridoma SN or human recombinant IL-1 alpha was able to substitute the hybridoma SN for the response. The reconstitution of the response by IL-1 and fixed P388D1 cells was inhibited by the addition of monoclonal anti-Ia antibody. These results indicate that IL-1 or fixed P388D1 cell does not exert a sufficient signal by itself and both of them are required for the reconstitution of a Con A response of highly purified T cells, and that Ia on fixed P388D1 cells play an important role.

Animals↗
PubMed1987

Mutant with diphtheria toxin receptor and acidification function but defective in entry of toxin.

A mutant of Chinese hamster ovary cells, GE1, that is highly resistant to diphtheria toxin was isolated. The mutant contains 50% ADP-ribosylatable elongation factor 2, but its protein synthesis was not inhibited by the toxin even at concentrations above 100 micrograms/ml. 125I-labeled diphtheria toxin was associated with GE1 cells as well as with the parent cells but did not block protein synthesis of GE1 cells even when the cells were exposed to low pH in the presence or absence of NH4Cl. The infections of GE1 cells and the parent cells by vesicular stomatitis virus were similar. GE1 cells were cross-resistant to Pseudomonas aeruginosa exotoxin A and so were about 1000 times more resistant to this toxin than the parent cells. Hybrids of GE1 cells and the parent cells or mutant cells lacking a functional receptor were more sensitive to diphtheria toxin than GE1 cells. These results suggest that entry of diphtheria toxin into cells requires a cellular factor(s) in addition to those involved in receptor function and acidification of endosomes and that GE1 cells do not express this cellular factor. This character is recessive in GE1 cells.

Animals↗
PubMed1987

Identification of a phenotype-specific enhancer in the first intron of the rat collagen II gene.

The regulation of the collagen II gene was investigated by transfecting plasmids containing potential regulatory sequences of this gene coupled to the gene for chloramphenicol acetyltransferase (CAT) into various cells. The 5' flanking region of this gene functioned as a weak promoter when transfected into chicken chondrocytes or fibroblasts. Inclusion of an 800-base fragment from the first intron, however, increased transcription of CAT approximately 18-fold in chicken chondrocytes and in differentiating limb bud cells but not in fibroblasts, myoblasts, muscle-derived fibroblasts, or teratocarcinoma cells. Furthermore, this fragment was active when placed either upstream or downstream of the CAT gene and when present in either orientation. The activity of this enhancer was examined in relation to differentiation by using "micromass" culture of limb bud mesenchyme cells undergoing chondrogenesis. In this system, no response to the enhancer was observed in undifferentiated limb bud mesenchyme cells. Following differentiation into chondrocytes, a 13-fold enhancer effect was observed in these cells. Finally, all-trans-retinoic acid, a known teratogen, dramatically suppressed enhancer activity in chondrocytes and differentiating limb bud mesenchyme cells. These results suggest that the collagen II gene contains an enhancer element in the first intron that is involved in cell-specific expression.

Animals↗
PubMed1987

Sequence of the cDNA encoding the laminin B1 chain reveals a multidomain protein containing cysteine-rich repeats.

Laminin is a basement membrane-specific glycoprotein (800 kDa) consisting of three chains: A, B1, and B2. Laminin has diverse biological functions, which include stimulating epithelial cell growth and differentiation. We have isolated two overlapping cDNA clones that span 5.9 kilobases and code for the entire B1 chain of mouse laminin. The nucleotide sequence of the clones reveals a 5358-base pair open reading frame that potentially codes for 1786 amino acids, including 20 amino acids of a presumptive signal peptide. Analysis of the deduced protein sequence predicts that the B1 chain has seven distinct domains that include cysteine-rich repeats, alpha-helical, and globular structures. Part of the cysteine-rich region is homologous to epidermal growth factor and other proteins that contain epidermal growth factor-like repeats.

Amino Acid Sequence↗