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Biomedical subjects

M Hatano

Publications and source records attributed to M Hatano.

At least 361 records · Page 20Linked to original sources
PubMed1982

Nasopharyngeal carcinoma in Japan--clinical evaluation of EBV serology and EBV-associated nuclear antigens test.

This study was aimed at the possible clinical application of two Epstein-Barr virus (EBV) immunological tests to Japanese nasopharyngeal carcinoma (NPC). One of them was serological test to measure antibody titers to EBV-associated antigens (viral capsid antigens (VCA) and virus-induced early antigens (EA)) of 42 NPC sera. The other was for the detection of EBV-associated nuclear antigens (EBNA) in 22 tumour cells of NPC. The results showed that significant elevation of antibody titers to VCA and EA which resided particularly in IgA class as well as a high incidence in the presence of EBNA were found in undifferentiated NPC. Apart from its importance in etiology, EBV serology and the EBNA test may help clinicians to establish a diagnosis of undifferentiated NPC in Japan and there is little doubt that these tests should eventually become a routine biologic test in ENT practice.

Adult↗
PubMed1982

Circular dichroism of bacteriochlorophyll a in light-harvesting bacteriochlorophyll-protein complexes from Rhodopseudomonas palustris.

Bacteriochlorophyll (Bchl)-protein complexes containing light-harvesting Bchls were isolated from Rhodopseudomonas palustris, and the CD spectra of these complexes were measured in the near-infrared region. These isolated Bchl-protein complexes retained the CD signals of light-harvesting Bchls that were observed in intracytoplasmic membrane preparation. Comparison of the CD spectrum of B870-reaction center complexes with that of the isolated reaction centers revealed that the peak at 860 nm and the trough at 890 nm were attributable to the B870 spectral form, and that the peak at 790 nm and the trough at 810 nm were not all attributable to the reaction center. The CD spectra of spectrally different types of B800--850 complex revealed that the magnitudes of the peak at 840--850 nm and the trough at 860--870 nm were correlated with the magnitude of the absorption peak at around 850 nm. Therefore, these positive and negative CD bands were attributable to the B850 spectral form. In a similar manner, the peak at 810--820 nm and trough at 790 nm were attributable to the B800 spectral form.

Bacterial Proteins↗
PubMed1982

Deuterium nuclear magnetic resonance spectroscopy of deuterated pyridine-iron(III) porphyrin complexes. Locations and relaxation times of bound deuterated pyridine resonances.

The first application of deuterium nuclear magnetic resonance spectroscopy (2H NMR) to fully deuterated pyridine (d5-pyridine)-iron(III) porphyrin complexes is described. (1) d5-Pyridine gives very broad 2H NMR signals in the presence of hemin or horseradish peroxidase to which pyridine is hardly (or not) bound, probably due to relatively long electronic relaxation times of the high-spin ferric ions. d5-Pyridine in the presence of horse-heart metmyoglobin gives resolved and less broadened 2H NMR signals, probably due to the relatively short electronic relaxation times of the ferric ion and/or to slow chemical exchange of the ligand. (2) The three resonances of free d5-pyridine coalesce into a single or a double resonance in the presence of a heme octapeptide prepared by trypsin digestion of Candida krusei cytochrome c. Nuclear spin-lattice and spin-spin relaxation times of the d5-pyridine-heme octapeptide complex are markedly shorter than those of free d5-pyridine. These findings are interpreted by the chemical exchange mechanism from the temperature dependences of the relaxation times. Thus, on certain assumptions the residence time of pyridine in the bound state and the exchange rate are estimated as approximately 10(-3) s and approximately 400 s-1, respectively, at 25 degrees C. Since 1H NMR signals of axial ligands of paramagnetic hemoproteins are hard to observe, the usefulness of deuterium magnetic resonance for investigating ligand exchange in the paramagnetic hemoproteins is emphasized.

Chemical Phenomena↗
PubMed1982

Development of protease activation mutants of HVJ (Sendai virus) in persistently infected cell cultures.

HVJ wild-type virus, in which the F protein is activated by trypsin but not by elastase, was spontaneously converted to a mutant with an F protein characterized by being activated by elastase alone. This spontaneous mutation generally occurred during serial passages of cells persistently infected with HVJ, even though the cells were first established by infection with plaque-purified wild-type virus. Multiple-cycle replication, plaque formation, haemolysis and SDS-polyacrylamide gel electrophoretic (SDS-PAGE) analysis showed that all the elastase-activated mutants isolated from HVJ carrier cells no longer required trypsin for F protein activation. At early passages, these protease activation mutants did not show temperature-sensitive (ts) growth, while at a later stage the mutants, together with the ts mutation, appeared dominant. The frequency of such a protease activation mutation during passage in the HVJ carrier cells seemed to depend on the cell species, but was increased when compared to lytic infections.

Animals↗
PubMed1982

Non-destructive detection of methionine sulfoxide in the resilium of a surf clam by solid-state 13C-NMR spectroscopy.

Methionine sulfoxide was detected in the resilium (internal hinge ligament) of a surf clam by high-resolution solid-state 13C-NMR spectroscopy involving cross-polarization and magic angle spinning, using no chemical procedure. The results support the previous report [Kikuchi, Y. and Tamiya, N. (1981) J. Biochem. (Tokyo) 89, 1975-1976] on a high content of methionine sulfoxide observed by chemical methods in the resilium protein of surf clam species.

Amino Acids↗
PubMed1982

Leukocyte adherence inhibition test in renal diseases.

Leukocyte adherence inhibition (LAI) test was examined in 35 patients with renal diseases and 14 normal controls, using collagenase-treated glomerular basement membrane, glycosidase-treated glomerular basement membrane and renal tubular epithelium as antigens. Although the control group showed strikingly similar mean LAI indices for all antigens tested, the whole group of patients with renal diseases showed a wide scatter of values. Two categories of patients had significantly increased LAI indices (p less than 0.01) when their mean values were compared with those of normal controls: (1) rapidly progressive glomerulonephritis (RPGN) and (2) lupus nephritis (SLE). In the serial studies of the RPGN and SLE cases, there were no significant changes in the pattern of LAI and they continued to give positive and very comparable results when re-examined at intervals of 1-6 months. Out of the 30 patients who were able to be evaluated with the three antigens, 15 cases exhibited positive LAI response to two or more antigens simultaneously. These in vitro findings suggest that there is an abnormal cellular response to certain antigen or widespread LAI reactivity to a variety of renal antigens in certain forms of human glomerulonephritis.

Antigens↗
PubMed1982

Concanavalin A-induced suppressor cell activity in focal glomerular sclerosis.

Suppressor cell activity (SCA) was analyzed in 8 patients with focal glomerular sclerosis (FGS) and 11 patients with chronic proliferative glomerulonephritis (CGN). We have assessed the ability of peripheral blood lymphocytes (PBL) stimulated by concanavalin A (Con A) to inhibit the proliferative response of normal allogeneic lymphocytes by both Con A and phytohemagglutinin (PHA). It was found that the FGS patients with nephrotic syndrome (NS) had significantly increased levels of suppression index when compared to the values obtained with normal controls. In contrast, the mean suppression values in the PBL from FGS patients in remission and CGN patients with or without NS, whether the mitogen used was Con A or PHA, were similar to those of the control subjects. Thus, the majority of FGS patients with NS demonstrated an alteration in Con A-induced SCA. The possible significance of these phenomena in the pathophysiology of FGS is discussed.

Adolescent↗