Effect of metallothionein on granulocyte chemotaxis and superoxide generation.
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Biomedical subjects
Publications and source records attributed to K Hanada.
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From a cultured broth of Streptomyces matensis A-6621, we isolated three new platelet aggregation inhibitors designated as PI-080, PI-085 and PI-087. The structures of these compounds were established by spectral and chemical methods.
Plasma concentration of ACTH and cortisol were measured at 15-min intervals from 22.30 to 07.00 h in 8 normal male volunteers. ACTH was measured both by a modified and sensitized isolated adrenal cell bioassay and by radioimmunoassay. Within-subject correlations between bioactive ACTH and cortisol concentrations ranged between 0.86 and 0.95, with an average correlation of 0.93 (86% shared variance). In contrast, within-subject correlations between immunoassayable ACTH and cortisol ranged between 0.03 and 0.92, with an average correlation of 0.69 (48% shared variance). These results suggest that plasma ACTH concentrations determined by RIA might not accurately reflect the capacity of plasma to regulate the secretion of adrenal glucocorticoids.
The purpose of this study was to evaluate the dento-craniofacial morphology and the occlusal characteristics in the Central American Indians from the dental-anthropological point of view. The sample consisted of cephalograms, pantomograms, dental casts, photos and records (anthropometric measurements and oral examinations) which were taken from 210 modern Central American Indians and 212 ancient Central American Indians. The results were summarized as follows: 1. Craniofacial morphology: The modern Central American Indians showed; (1) smaller facial height and shorter depth of the cranial base and jaws than those of the Caucasians. (2) posterior position of peri-orbital structures, and smaller values of anterior facial height in comparison with the Japanese, which were similar to the Peruvian Indians. (3) shorter depth of the jaws and prominence of the chin than the ancient Central American Indians. 2. Dental arch form and tooth size: The modern Central American Indians had; (1) wider dental arches than the Caucasians, while sharing similar values with the Peruvian Indians and the Japanese. (2) smaller incisors, larger premolars and molars in the mesio-distal crown diameter compared with the Caucasians. (3) smaller teeth in the mesio-distal crown diameter than the ancient Central American Indians. 3. Occlusal conditions: The modern Central American Indians showed a good mesio-distal relationship between the upper and lower first molars in 70 percent.
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Immune activities of newly developed, short-lived SAM-P/1 mice declined sharply after a few months of age. As early as 2 months of age, the activity of T-helper (Th) cells ('Th2'-like) in the in vitro primary antibody response was profoundly impaired, in contrast to normal activity of Th cells ('Th1'-like) engaged in cell-mediated immune responses. Thus, young SAM-P/1 mice show a functional heterogeneity of Th cells. To determine how such a 'Th2' abnormality is inherited in SAM-P/1 mice, immune activities of their hybrids and backcrosses between MHC-identical, high responder B10.BR mice were statistically assessed. The distribution of responses did not support the Mendelian single-gene determination for low responsiveness. Moreover, involvement of a single gene which exhibits incomplete dominance was ruled out because of a continuous distribution pattern of antibody response in the F2 generation. Such an analysis strongly suggests that the impaired 'Th2'-like activity of SAM-P/1 mice is under control of two genes, based on the proportion of low responders in F2 hybrids (29 out of 267, 10.8%) and on calculation according to Wright's formula (n = 1.72). Further linkage analyses suggest that one of the genes is closely linked to albino coat-colour (c) locus on chromosome 7. The putative two genes are likely to control 'differentiation' or 'maturation' of Th2-like cells defectively, but the defect is not refractory, because in vivo-primed Th cells function in vitro as do those in ordinary strains of mice. Possible mechanisms and biological significance in relation to loss of immune activity with ageing are discussed.
In seven subjects with unilateral cleft lip and palate (UCLP), two subjects without cleft but with complete lingual crossbite, and two subjects with normal occlusion, tongue contact patterns against the hard palate, lingual surfaces of maxillary and mandibular teeth, and mandibular lingual mucosa during swallowing were analyzed three-dimensionally using electropalatography (EPG), before and after lateral expansion of the maxillary dental arch and after 3 months of retention. Before maxillary lateral expansion, all of the subjects with cleft palate showed no palate-tongue contact at rest, and limited movement of the tongue anteriorly and upward through the entire swallow cycle. Furthermore, the tongue contacted the hard palate for a relatively brief time during swallowing compared with the subjects without cleft with normal occlusion. After expansion, the tongue was seen to contact all areas of the hard palate and the lingual surface of the maxillary dentition for a longer period of time. After 3 months of retention, the tongue maintained contact with all lingual areas of the mandibular and maxillary arches and the hard palate.
We previously constructed a bifunctionally active membrane-bound fusion protein, in which Escherichia coli proline carrier (the product of the putP gene) was linked with beta-galactosidase (the product of the lacZ gene) through a collagen linker (Hanada, K., Yamato, I., and Anraku, Y. (1987) J. Biol. Chem. 262, 14100-14104). The proline carrier was purified from this site specifically cleavable fusion protein. Cytoplasmic membranes overproducing the fusion protein were solubilized with dodecylmaltoside, and the solubilized fraction was subjected to anti-beta-galactosidase IgG-Sepharose chromatography. The fusion protein was specifically adsorbed to the immunoaffinity resin and then treated with collagenase for splitting the proline carrier moiety of the fusion protein from the beta-galactosidase moiety. The collagenase used for the collagenolysis was then removed by anti-collagenase IgG-Sepharose chromatography. In this way, the proline carrier was purified to more than 95% homogeneity of the protein. Proline transport in proteoliposomes reconstituted with the purified carrier was dependent on the membrane potential and the chemical gradient of Na+ across the membrane with apparent Michaelis constants for proline and for Na+ stimulation of 3.6 microM and 31 microM, respectively. These results indicated that the proline carrier mediates electrogenic Na+/proline symport.
Proline carrier of Escherichia coli was extracted from the carrier-overproducing membranes with dodecylmaltoside in the presence of phospholipid. The solubilized carrier showed the same proline binding activity as that in normal membranes. As judged from determinations of the binding activity in the micellar state as a marker of active carrier and the radioactivity of N-[ethyl-2-3H]ethylmaleimide-labeled carrier as a marker of carrier polypeptide, 80% of the carrier molecules in the membranes were extracted. Optimal conditions for reconstitution of the solubilized carrier were established. By a combination of freeze-thawing, sonication and dilution procedures, 70% of the solubilized carrier molecules were incorporated into proteoliposomes and the restored active transport of proline showed an apparent Kt of 1 microM and turnover number of 0.6 s-1. The transport of proline was driven by a membrane potential in a Na+ (or Li+)-dependent manner.
Complete nucleotide sequences of two new satellite RNAs (satRNA) of cucumber mosaic virus (CMV), E-satRNA and OY2-satRNA, have been determined and compared with known satellite RNA sequences. E-satRNA contained 339 nucleotide residues and OY2-satRNA had 386 nucleotide residues. Comparison of the sequences among satRNAs including these new satRNAs revealed extensive homologous regions in the 5'-terminus and the 3'-half. The former region contains about 95 nucleotide residues (80-100% homology) and the latter has about 175 nucleotide residues (81-99% homology), but there was less homology in the middle of the RNA. A possible secondary structure for E-satRNA, OY2-satRNA, and Y-satRNA [S. Hidaka et al. (1984) FEBS Lett. 174, 38-42] was constructed and compared with that of a satellite RNA from CMV-Q (Q-satRNA) [K. H. J. Gordon and R. H. Symons (1983), Nucl. Acids Res. 11, 947-960]. Two similar hairpin-loop structures in the 5'-terminal region were common features of the RNAs; one of them was found in E-satRNA, the other in OY2-satRNA, and both in Y-satRNA and Q-satRNA. Analyses of in vitro messenger properties of the satRNAs suggested that the first open reading frame of E-sat and Y-satRNAs was a possible coding region for protein synthesis.
Stability of the mandible was analysed with a Xerox copy of the dental cast in 35 cases of mandibular prognathism corrected by ramus osteotomies. The occlusal relationship in the Xerox copy was illustrated by superimposing two contact points on the upper and lower dental arches and the change in the position of the lower dental arch in relation to the upper dental arch was obtained by superimposing the latter on preoperative, predicted postoperative, and six months postoperative occlusions. The stability of the mandible was analysed by measuring the movement of five landmarks (two posterior, two molar and one incisor points) set around the lower dental arch to represent the movement of the mandible. The relapse was estimated by the movements of the landmarks from the predicted postoperative occlusion to the six months postoperative occlusion. The mean estimated anterior relapses at the posterior and molar points with the larger predicted movement and the incisor point were between 0.9 mm. and 2.0 mm. at six months postoperatively, whereas on the side with the smaller predicted movement, the points moved posteriorly by 0.6 mm. and 0.5 mm. Despite the fact that the amount of the predicted lateral movement was much smaller than that of the predicted posterior movement at operation, the posterior points were estimated to relapse laterally by 2.0 mm. and 1.7 mm.(ABSTRACT TRUNCATED AT 250 WORDS)
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A purification procedure of cathepsin H from human kidney is presented. It includes gel filtration, ion exchange chromatography, and covalent chromatography on thiol Sepharose as an essential step. Purified cathepsin H emerges in an isoelectric focusing gel at pH 6.1 and 6.3. Polyacrylamide gel electrophoresis in the presence of sodium dodecyl sulphate shows a molecular mass of about 28 kDa. Less than 20% of the enzyme preparation can be separated into a heavy (24 kDa) and a light chain (4 kDa) after reduction and gel filtration on Sephacryl S-200. The partial amino-acid sequence of human cathepsin H shows its close similarity to rat cathepsin H. Inhibition constants (Ki) of cathepsins H and B with chicken cystatin, two forms of human stefin A, human stefin B, and two forms of human cystatin C are in the range of 10(-9) to 10(-11)M.